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15. 12. 2025 Jan Kříž

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If you do not have it available in your CMS, please email webmaster@vscht.cz.<\/p>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"116987":{"idvazba":"144406","nad_uzel":"116983","pod_uzel":"116987","url":"\/about","sablona":"49","nazev":"About department","_url_prefix":"{\/\/uoch.vscht.cz\/about}","poradi":"1","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.039431","platne_do":null,"iduzel":"116987","obsah":"a:14:{s:5:\"nazev\";s:16:\"About department\";s:9:\"seo_title\";s:16:\"About department\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["116988","116989","116990"],"poduzly_count":3,"poduzly_count_aut":2,"poduzly":{"poduzly_count_aut_sum":0,"116988":{"idvazba":"144407","nad_uzel":"116987","pod_uzel":"116988","url":"","sablona":"4","nazev":"[box] v\u00fdpis pod\u0159\u00edzen\u00fdch str\u00e1nek","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.048413","platne_do":null,"iduzel":"116988","obsah":"a:6:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:5:\"false\";s:10:\"podstranky\";s:4:\"true\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:0:\"\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"116989":{"idvazba":"144408","nad_uzel":"116987","pod_uzel":"116989","url":"\/about\/profile","sablona":"49","nazev":"Profile and history of the department","_url_prefix":"{\/\/uoch.vscht.cz\/about\/profile}","poradi":"1","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.055781","platne_do":null,"iduzel":"116989","obsah":"a:13:{s:5:\"nazev\";s:37:\"Profile and history of the department\";s:9:\"seo_title\";s:37:\"Profile and history of the department\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:118:\"<h2>Profile of the department<\/h2>\r\n<p>V\u011bnujeme se tomu a onomu.<\/p>\r\n<h2>History<\/h2>\r\n<p>\u00dastav byl zalo\u017een...<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"116990":{"idvazba":"144409","nad_uzel":"116987","pod_uzel":"116990","url":"\/about\/members","sablona":"49","nazev":"Members","_url_prefix":"{\/\/uoch.vscht.cz\/about\/members}","poradi":"2","skupina_www":"everyone","platne_od":"08.06.2026 20:26:00","platne_do":null,"iduzel":"116990","obsah":"a:13:{s:5:\"nazev\";s:25:\"Members of the Department\";s:9:\"seo_title\";s:7:\"Members\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:6288:\"<h2><\/h2>\r\n<h2>Department Administration<\/h2>\r\n<ul>\r\n<li><strong>Head of Department<\/strong>: Prof. Ing. Radek Cibulka, PhD. (<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/504\">contact<\/a>)<\/li>\r\n<li><strong>Secretary of Department:<\/strong> Ing. Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1, Ph.D. (<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/693\">contac<\/a><a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/693\">t<\/a>)<\/li>\r\n<li><strong>Economist of Department: <\/strong>Ing. Mark\u00e9ta Slabochov\u00e1<span>&nbsp;<\/span> (<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/415\">contact<\/a>)<\/li>\r\n<li><strong>Administrative Support&nbsp;of Department:<\/strong> Veronika P\u00edpalov\u00e1 <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/2137\">(contact)<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<hr>\r\n<h2>Professors<\/h2>\r\n<ul>\r\n<li>prof. <strong>Andrea Brancale<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/3531\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>prof. Ing. <strong>Radek Cibulka<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/504\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>prof. Ing.&nbsp;<strong>Michal Kohout<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/679\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>prof. Ing. <strong>Jaroslav Kv\u00ed\u010dala<\/strong>, CSc. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/224\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>prof. Ing. <strong>Pavel Lhot\u00e1k<\/strong>, CSc. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/341\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>prof. Ing. <strong>Ji\u0159\u00ed Svoboda<\/strong>, CSc. \u2013 <a href=\"#\">webov\u00fd profil<\/a><\/li>\r\n<\/ul>\r\n<hr>\r\n<h2>Associate professors<\/h2>\r\n<ul>\r\n<li>doc. Ing. <strong>Jan Budka<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/362\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>doc. Ing.&nbsp; <strong>Petr Kova\u0159\u00ed\u010dek<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/3102\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>doc. Ing. <strong>Tom\u00e1\u0161 Tobrman<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/611\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<\/ul>\r\n<hr>\r\n<h2>Lecturers<\/h2>\r\n<ul>\r\n<li>Ing. <strong>Petra Cu\u0159\u00ednov\u00e1<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/3520\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. Bc. <strong>Michal Himl<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/630\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Mgr.&nbsp;<strong>Roman Holakovsk\u00fd<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/431\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>V\u00e1clav Kozm\u00edk<\/strong>, CSc. \u2013&nbsp;<a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/278\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Martin Krupi\u010dka<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/670\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Ond\u0159ej Kundr\u00e1t<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/733\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Petra M\u00e9nov\u00e1<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/1810\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Mgr. et Mgr. <strong>Pavla Perl\u00edkov\u00e1<\/strong>, Ph.D. \u2013&nbsp;<a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/3110\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/3110\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Eva Svobodov\u00e1<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/634\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Martin Tlust\u00fd<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/1917\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Ji\u0159\u00ed T\u016fma<\/strong>, Ph.D. \u2013 <a href=\"#\">webov\u00fd profil<\/a> | <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/1006\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<\/ul>\r\n<hr>\r\n<h2>Technicians<\/h2>\r\n<ul>\r\n<li><strong>Kv\u011bta B\u00e1rtov\u00e1<\/strong> \u2013 <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/540\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Tom\u00e1\u0161 Hlo\u017eek \u2013<\/strong>&nbsp;<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/4085\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Zde\u0148ka Hrb\u00e1\u010dkov\u00e1<\/strong> \u2013 <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/1328\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Michaela Kadlecov\u00e1&nbsp;<\/strong> \u2013&nbsp;<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/442\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Martina Kovandov\u00e1 <\/strong>\u2013<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/477\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Nataliia Markovska<\/strong> \u2013<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/4092\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li>Ing. <strong>Mark\u00e9ta Slabochov\u00e1<\/strong><span>&nbsp;<\/span>\u2013<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/415\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Helena \u0160tenglov\u00e1<\/strong><span>&nbsp;<\/span>\u2013<a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/486\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><\/li>\r\n<li><strong>Marta Tok\u00e1rov\u00e1<\/strong> \u2013 <a href=\"https:\/\/telefony.vscht.cz\/en\/Person\/391\" target=\"_blank\" rel=\"noopener\">phonebook<\/a><br>\r\n<h2><br><br><\/h2>\r\n<h2><br><a href=\"https:\/\/telefony.vscht.cz\/en\/Department\/9\">Department Phonebook<\/a><\/h2>\r\n<\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"116991":{"idvazba":"144410","nad_uzel":"116983","pod_uzel":"116991","url":"\/students","sablona":"49","nazev":"Studying","_url_prefix":"{\/\/uoch.vscht.cz\/students}","poradi":"2","skupina_www":"everyone","platne_od":"02.02.2026 21:25:00","platne_do":null,"iduzel":"116991","obsah":"a:14:{s:5:\"nazev\";s:8:\"Studying\";s:9:\"seo_title\";s:8:\"Studying\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["122057","122061","116992","116993","116994"],"poduzly_count":5,"poduzly_count_aut":2,"poduzly":{"poduzly_count_aut_sum":0,"122057":{"idvazba":"150076","nad_uzel":"116991","pod_uzel":"122057","url":"","sablona":"52","nazev":"Information for Bachelor students","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"02.02.2026 21:25:00","platne_do":null,"iduzel":"122057","class":"accordion","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"122061":{"idvazba":"150080","nad_uzel":"116991","pod_uzel":"122061","url":"","sablona":"52","nazev":"Information for Master students","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.02.2026 21:22:00","platne_do":null,"iduzel":"122061","class":"accordion","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"116992":{"idvazba":"144411","nad_uzel":"116991","pod_uzel":"116992","url":"","sablona":"4","nazev":"[box] v\u00fdpis pod\u0159\u00edzen\u00fdch str\u00e1nek","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.077403","platne_do":null,"iduzel":"116992","obsah":"a:6:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:5:\"false\";s:10:\"podstranky\";s:4:\"true\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:0:\"\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"116993":{"idvazba":"144412","nad_uzel":"116991","pod_uzel":"116993","url":"\/students\/prospective-students","sablona":"49","nazev":"Prospective students","_url_prefix":"{\/\/uoch.vscht.cz\/students\/prospective-students}","poradi":"3","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.084384","platne_do":null,"iduzel":"116993","obsah":"a:13:{s:5:\"nazev\";s:38:\"Prospective students at the Department\";s:9:\"seo_title\";s:20:\"Prospective students\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:1378:\"<h2 style=\"text-align: justify;\">Master\u2019s Degree<\/h2>\r\n<p>Information about master proigramme<\/p>\r\n<hr>\r\n<h2 style=\"text-align: justify;\"><span>Doctoral (Ph.D.) study<\/span><\/h2>\r\n<p style=\"text-align: justify;\">Doctoral studies are research-oriented and aim to prepare students for independent scientific work in academia or industry.<\/p>\r\n<ul style=\"text-align: justify;\">\r\n<li>Duration: 4 years full-time, up to 7 years part-time<\/li>\r\n<li>Mode of study: Full-time (internal) or Part-time (external)<\/li>\r\n<li>Degree awarded: Ph.D. (\u201cdoktor\u201d in Czech)<\/li>\r\n<\/ul>\r\n<hr>\r\n<h2 style=\"text-align: justify;\">Exchange and Visiting Students<\/h2>\r\n<p style=\"text-align: justify;\">The Department of International Relations assists foreign students participating in short-term study stays based on agreements between universities, governments, or organizations. These students follow a learning agreement approved by their home institutions and do not receive a diploma from UCT Prague.<\/p>\r\n<p style=\"text-align: justify;\">Examples of exchange and visiting programmes:<\/p>\r\n<ul style=\"text-align: justify;\">\r\n<li>Erasmus+<\/li>\r\n<li>IAESTE<\/li>\r\n<li>ATHENS<\/li>\r\n<li>CEEPUS<\/li>\r\n<li>AKTION<\/li>\r\n<li>...and others.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\">More <a href=\"https:\/\/incoming.vscht.cz\/\">information for incoming students<\/a> by International Relations Office<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"116994":{"idvazba":"144413","nad_uzel":"116991","pod_uzel":"116994","url":"\/students\/current-students","sablona":"49","nazev":"Current students","_url_prefix":"{\/\/uoch.vscht.cz\/students\/current-students}","poradi":"4","skupina_www":"everyone","platne_od":"15.12.2025 13:38:25.092984","platne_do":null,"iduzel":"116994","obsah":"a:13:{s:5:\"nazev\";s:16:\"Current students\";s:9:\"seo_title\";s:16:\"Current students\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:696:\"<h2 style=\"text-align: justify;\">Information for Bachelor &amp; Master Students<\/h2>\r\n<h3>University wide<\/h3>\r\n<ul>\r\n<li>Website <a href=\"https:\/\/study.vscht.cz\/studying-at-uct\">study.vscht.cz<\/a><\/li>\r\n<\/ul>\r\n<h3 style=\"text-align: justify;\"><strong>Department - specific<\/strong><\/h3>\r\n<p>Nothing is here right now<\/p>\r\n<p>&nbsp;<\/p>\r\n<h2 style=\"text-align: justify;\">Information for PhD Students<\/h2>\r\n<h3 style=\"text-align: justify;\"><strong>University wide<\/strong><\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Website <a href=\"https:\/\/phd.vscht.cz\">phd.vscht.cz<\/a><\/li>\r\n<\/ul>\r\n<h3 style=\"text-align: justify;\"><strong>Department - specific<\/strong><\/h3>\r\n<p>Nothing is here right now<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"116995":{"idvazba":"164109","nad_uzel":"116983","pod_uzel":"116995","url":"\/research","sablona":"49","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research}","poradi":"3","skupina_www":"everyone","platne_od":"30.06.2026 12:28:00","platne_do":null,"iduzel":"116995","obsah":"a:14:{s:5:\"nazev\";s:26:\"Research at the department\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:49:\"<p>Text about department research in 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activity.<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:9:\"modrabox2\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"122005":{"idvazba":"150021","nad_uzel":"122004","pod_uzel":"122005","url":"","sablona":null,"nazev":"Cibulka","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"10.06.2026 21:23:00","platne_do":null,"iduzel":"122005","obsah":"a:17:{s:6:\"nadpis\";s:19:\"Prof. Radek Cibulka\";s:5:\"odkaz\";s:17:\"\/research\/cibulka\";s:11:\"targetblank\";s:1:\"1\";s:11:\"text_odkazu\";s:22:\"Cibulka research group\";s:5:\"perex\";s:161:\"<p><strong>Photocatalysis and organocatalysis<\/strong><\/p>\r\n<p>Design of catalytic systems using light 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Prof. Petr Kova\u0159\u00ed\u010dek\";s:5:\"odkaz\";s:20:\"https:\/\/www.pklab.cz\";s:11:\"targetblank\";s:1:\"1\";s:11:\"text_odkazu\";s:30:\"Dynamic Covalent Chemistry\ud83e\udc75\";s:5:\"perex\";s:145:\"<p><strong>Dynamic Covalent Chemistry<\/strong><\/p>\r\n<p>Research on adaptive materials and molecular machines based on dynamic covalent bonds.<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:8:\"oranzova\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133690":{"idvazba":"164147","nad_uzel":"122004","pod_uzel":"133690","url":"","sablona":null,"nazev":"krupicka","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"10.06.2026 21:36:00","platne_do":null,"iduzel":"133690","obsah":"a:16:{s:6:\"nadpis\";s:20:\"Dr. Martin Krupi\u010dka\";s:5:\"odkaz\";s:19:\"\/research\/krupicka\/\";s:11:\"text_odkazu\";s:24:\"Krupi\u010dka research group\";s:5:\"perex\";s:175:\"<p><strong>Mechanochemistry and computational chemistry<\/strong><\/p>\r\n<p>Covalent mechanochemistry, solid state synthesis in ball mills, quantum chemistry, green chemistry<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:10:\"zelenabox2\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133691":{"idvazba":"164148","nad_uzel":"122004","pod_uzel":"133691","url":"","sablona":null,"nazev":"kvicala","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"11.06.2026 09:05:00","platne_do":null,"iduzel":"133691","obsah":"a:16:{s:6:\"nadpis\";s:51:\"Dr. Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1, Prof. Jaroslav Kv\u00ed\u010dala\";s:5:\"odkaz\";s:18:\"\/research\/kvicala\/\";s:11:\"text_odkazu\";s:24:\"Organofluorine Chemistry\";s:5:\"perex\";s:150:\"<p><strong>Organofluorine Chemistry<\/strong><\/p>\r\n<p>Synthesis of fluorinated organic compounds and study of their reactivity in radical reactions<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:8:\"sedabox2\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133692":{"idvazba":"164149","nad_uzel":"122004","pod_uzel":"133692","url":"","sablona":null,"nazev":"lhotak-budka","_url_prefix":null,"poradi":"6","skupina_www":"everyone","platne_od":"10.06.2026 21:40:00","platne_do":null,"iduzel":"133692","obsah":"a:16:{s:6:\"nadpis\";s:43:\"Prof. Pavel Lhot\u00e1k, Assoc. Prof. Jan Budka\";s:5:\"odkaz\";s:23:\"\/research\/lhotak-budka\/\";s:11:\"text_odkazu\";s:24:\"Supramolecular Chemistry\";s:5:\"perex\";s:175:\"<p><strong>Supramolecular chemistry<\/strong><\/p>\r\n<p>Synthesis of calixarenes, thiacalixarenes and related macrocycles for molecular recognition and supramolecular systems<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:0:\"\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133693":{"idvazba":"164150","nad_uzel":"122004","pod_uzel":"133693","url":"","sablona":null,"nazev":"menova","_url_prefix":null,"poradi":"7","skupina_www":"everyone","platne_od":"10.06.2026 22:47:00","platne_do":null,"iduzel":"133693","obsah":"a:16:{s:6:\"nadpis\";s:18:\"Dr. Petra M\u00e9nov\u00e1\";s:5:\"odkaz\";s:17:\"\/research\/menova\/\";s:11:\"text_odkazu\";s:16:\"Chemical Biology\";s:5:\"perex\";s:161:\"<p><strong>Medicinal Chemistry and Glycochemistry<\/strong><\/p>\r\n<p>Synthesis of ligands for lectin receptors, structure\u2014activity relationship (SAR) studies<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:9:\"modrabox2\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133694":{"idvazba":"164151","nad_uzel":"122004","pod_uzel":"133694","url":"","sablona":null,"nazev":"perlikova","_url_prefix":null,"poradi":"8","skupina_www":"everyone","platne_od":"10.06.2026 23:25:00","platne_do":null,"iduzel":"133694","obsah":"a:16:{s:6:\"nadpis\";s:21:\"Dr. Pavla Perl\u00edkov\u00e1\";s:5:\"odkaz\";s:20:\"\/research\/perlikova\/\";s:11:\"text_odkazu\";s:19:\"Medicinal Chemistry\";s:5:\"perex\";s:141:\"<p><strong>Medicinal Chemistry<\/strong><\/p>\r\n<p>Synthesis of biologically active compounds inspired by natural products and other sources<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:12:\"zlutosedabox\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"139483":{"idvazba":"171587","nad_uzel":"122004","pod_uzel":"139483","url":"","sablona":null,"nazev":"tlusty","_url_prefix":null,"poradi":"9","skupina_www":"everyone","platne_od":"10.06.2026 23:26:00","platne_do":null,"iduzel":"139483","obsah":"a:16:{s:6:\"nadpis\";s:18:\"Dr. Martin Tlust\u00fd\";s:5:\"odkaz\";s:16:\"\/research\/tlusty\";s:11:\"text_odkazu\";s:19:\"Reticular chemistry\";s:5:\"perex\";s:139:\"<p><strong>Supramolecular and reticular chemistry<\/strong><\/p>\r\n<p>Mechanically interlocked molecules and chemistry of porous materials<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:6:\"zelena\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"133695":{"idvazba":"164152","nad_uzel":"122004","pod_uzel":"133695","url":"","sablona":null,"nazev":"tobrman","_url_prefix":null,"poradi":"10","skupina_www":"everyone","platne_od":"10.06.2026 23:27:00","platne_do":null,"iduzel":"133695","obsah":"a:16:{s:6:\"nadpis\";s:28:\"Assoc. Prof. Tom\u00e1\u0161 Tobrman\";s:5:\"odkaz\";s:18:\"\/research\/tobrman\/\";s:11:\"text_odkazu\";s:24:\"Organometallic Synthesis\";s:5:\"perex\";s:185:\"<p><strong>Organometallic Chemistry<\/strong><\/p>\r\n<p>Transition metal-catalyzed reactions, the chemistry of organophosphorus compounds, and the stereoselective synthesis of alkenes.<\/p>\";s:7:\"skupina\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:8:\"velikost\";s:1:\"4\";s:5:\"sirka\";s:1:\"4\";s:5:\"vyska\";s:4:\"auto\";s:8:\"pozice_x\";s:1:\"1\";s:8:\"pozice_y\";s:0:\"\";s:12:\"barva_pozadi\";s:8:\"sedabox2\";s:11:\"smer_pozadi\";s:11:\"gradient-no\";s:10:\"smer_textu\";s:6:\"nahoru\";s:9:\"countdown\";s:0:\"\";s:14:\"obrazek_pozadi\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0}}},"136559":{"idvazba":"167926","nad_uzel":"116995","pod_uzel":"136559","url":"\/research\/brancale","sablona":"49","nazev":"Andrea Brancale Research Group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/brancale}","poradi":"1","skupina_www":"everyone","platne_od":"03.06.2026 13:43:00","platne_do":null,"iduzel":"136559","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:30:\"Andrea Brancale Research Group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:28:\"0001~~8_R1jze1NDPTMNQEAA.jpg\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:2466:\"<h2 style=\"text-align: center;\" class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\"><\/span><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\"><\/span><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\">Prof. Andrea Brancale,&nbsp; Dr. Petra Cu\u0159\u00ednov\u00e1<o:p><\/o:p><\/span><\/h2>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\"><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Our research focus is on the design, synthesis, and development of novel biologically active molecules, in particular, but not exclusively, of anticancer and antiviral compounds. Our main objective is to contribute towards the discovery and the development of new therapies against diseases with a clear unmet medical need. To achieve this, we combine a variety of drug design and approaches, from classical medicinal chemistry to more advanced computer-based drug design methods. The highly interdisciplinary and collaborative nature of our research is reflected in our publications, and through the extensive network of collaboration we have established during the years.<br><br><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\"><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 13.0pt; font-family: 'Arial',sans-serif; mso-fareast-font-family: 'Times New Roman'; color: #383735; mso-fareast-language: EN-GB;\"><img src=\"\/files\/uzel\/0136559\/0001~~8_R1jze1NDPTMNQEAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 IMG_5966(1) (jpg) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"800\" height=\"600\"><\/span><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["65402","65404","136560","136561"],"poduzly_count":4,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":0,"65402":{"idvazba":"167910","nad_uzel":"136561","pod_uzel":"65402","url":"","sablona":"4","nazev":"Brancale Research Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:03:00","platne_do":null,"iduzel":"65402","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"65404":{"idvazba":"167905","nad_uzel":"136559","pod_uzel":"65404","url":"\/research\/brancale\/people","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/brancale\/people}","poradi":"2","skupina_www":"everyone","platne_od":"13.10.2025 11:04:00","platne_do":null,"iduzel":"65404","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:31729:\"<h2><strong>Staff:<\/strong>&nbsp; &nbsp;<\/h2>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 100%; background-color: #ffffff; border: 0px hidden #FFFFFF;\"><colgroup><col style=\"width: 30.6726%;\"><col style=\"width: 34.6467%;\"><col style=\"width: 34.6467%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-color: rgb(255, 255, 255);\">\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255);\"><img src=\"\/images\/215!215\/uzel\/0065404\/0010~~S8xLKUpNBAA.jpg\" alt=\" \u25f3 andrea (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-color: rgb(255, 255, 255); border-width: 0px; background-color: rgb(255, 255, 255);\">\r\n<p><strong><br>Prof. Andrea Beancale<\/strong><\/p>\r\n<p><strong><br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255);\">\r\n<p><\/p>\r\n<p><\/p>\r\n<p><br>phone:<\/p>\r\n<p>&nbsp;+420 220 442 931<\/p>\r\n<p><br>e-mail:<\/p>\r\n<p><a href=\"mailto:brancala@vscht.cz\">brancala@vscht.cz<\/a><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-width: 0px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0027~~K0gtKUoEAA.jpg\" alt=\" \u25f3 petra (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255); border-width: 0px;\">\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong>Dr. Petra Cu\u0159\u00ednov\u00e1<\/strong><\/p>\r\n<p><strong><br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-width: 0px;\">\r\n<p><br>phone:<\/p>\r\n<p>&nbsp;+420 220 442 930<\/p>\r\n<p><br>e-mail:<\/p>\r\n<p><a href=\"mailto:curinovp@vscht.cz\">curinovp@vscht.cz<\/a>&nbsp;&nbsp;<\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<h2><strong><br>Technician:<br><br><\/strong><\/h2>\r\n<table style=\"border-collapse: collapse; width: 100%;\" border=\"1\"><colgroup><col style=\"width: 30.5426%;\"><col style=\"width: 34.5736%;\"><col style=\"width: 34.5736%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-color: rgb(255, 255, 255);\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0009~~MzI1NYtPSjE2N9FNTizKT0nNystMTgUA.jpg\" alt=\" \u25f3 2556_bd374-carodejnice (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-color: rgb(255, 255, 255);\">\r\n<p><strong><br>Zde\u0148ka Hrb\u00e1\u010dkov\u00e1<\/strong><\/p>\r\n<p><strong><br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td>\r\n<p><\/p>\r\n<p><br>e-mail:<\/p>\r\n<p>Zdenka.Hrbackova@vscht.cz<\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><strong><\/strong><\/p>\r\n<h2><strong>Post-Docs:<\/strong><\/h2>\r\n<p><strong><\/strong><\/p>\r\n<table border=\"1\" height=\"54\" class=\"table_ bezramecku\" style=\"border-collapse: collapse; width: 78.7655%; height: 634.332px; background-color: #ffffff; border: 0px hidden #FFFFFF;\"><colgroup><col style=\"width: 55.2063%;\"><col style=\"width: 44.7937%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"height: 154.083px; border-style: none;\">\r\n<td style=\"height: 154.083px; border-width: 0px; border-color: rgb(255, 255, 255);\"><img src=\"\/images\/215!215\/uzel\/0065404\/0028~~K0ktyk4EAA.jpg\" alt=\" \u25f3 terka (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); height: 154.083px; border-style: none; background-color: rgb(255, 255, 255);\">\r\n<p><strong><br>Dr. Tereza Hor\u00e1\u010dkov\u00e1<\/strong><\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px; background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-style: none;\">\r\n<td style=\"height: 154.083px; border-width: 0px; border-color: rgb(255, 255, 255);\"><img src=\"\/images\/215!215\/uzel\/0065404\/0029~~K8pPSi0qAQA.jpg\" alt=\" \u25f3 robert (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<p><strong><br>Dr. R\u00f3bert Obert\u00edk<\/strong><\/p>\r\n<p><strong>&nbsp;<br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0004~~C_bxBwA.png\" alt=\" \u25f3 SLO (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255); border-style: hidden; height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0040~~805MzDMEAA.jpg\" alt=\" \u25f3 Kaan1 (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255); border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br>Dr. Kaan Birg\u00fcl<\/strong><\/p>\r\n<p><strong><br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0041~~Kyktyk6tBAA.png\" alt=\" \u25f3 turkey (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"36\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255); border-style: none; height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0042~~800sykzMy0sEAA.jpg\" alt=\" \u25f3 Marianna (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-width: 0px; border-color: rgb(255, 255, 255); background-color: rgb(255, 255, 255); border-style: none; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br>Dr. Marianna Bufano<\/strong><\/p>\r\n<p><strong><br><br><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<h2><strong>&nbsp;<\/strong><\/h2>\r\n<h2><strong>Permanent PhD. students:<br><br><\/strong><strong><\/strong><\/h2>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 79.2297%;\"><colgroup><col style=\"width: 54.9058%;\"><col style=\"width: 45.0697%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-style: none;\">\r\n<td>\r\n<h2>2<sup>nd<\/sup>&nbsp;year:<\/h2>\r\n<\/td>\r\n<td><\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none;\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0043~~80rM9gAA.jpg\" alt=\" \u25f3 JakH (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td><strong><br>Jakub Harvalik<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<h2><strong><br>Permanent Master students:<br><br><\/strong><\/h2>\r\n<h2><\/h2>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 79.2297%;\"><colgroup><col style=\"width: 54.8947%;\"><col style=\"width: 45.0451%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-style: none;\">\r\n<td>\r\n<h2>2<sup>nd<\/sup> year:<br><br><\/h2>\r\n<p><\/p>\r\n<p><img src=\"\/images\/215!215\/uzel\/0065404\/0030~~KykAAA.jpg\" alt=\" \u25f3 tp (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/p>\r\n<\/td>\r\n<td>\r\n<p><\/p>\r\n<p><\/p>\r\n<p><\/p>\r\n<p><strong><br><br><br>Tereza Pazourov\u00e1<br><br><\/strong><strong><\/strong><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0004~~C_bxBwA.png\" alt=\" \u25f3 SLO (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 154px; background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0019~~y0rMSwQA.jpg\" alt=\" \u25f3 jana (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154px; text-align: left; background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-style: hidden;\"><strong><br>Jana Ferenczeiov\u00e1<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 154px; background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0016~~y8jPq0oEAA.jpg\" alt=\" \u25f3 honza (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154px; background-color: rgb(255, 255, 255); border-color: rgb(255, 255, 255); border-style: hidden;\">\r\n<p><strong><br>Jan Drahor\u00e1d<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 154px; border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0021~~y0nNy04EAA.jpg\" alt=\" \u25f3 lenka (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154px; border-style: hidden;\"><strong><br>Lenka Vondr\u00e1\u010dkov\u00e1<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 154px; border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0012~~S8zLSwQA.jpg\" alt=\" \u25f3 anna (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154px; border-style: hidden;\"><strong><br>Anna Velebov\u00e1<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\">\r\n<p><img src=\"\/images\/215!215\/uzel\/0065404\/0044~~c8vMySxwBgA.jpg\" alt=\" \u25f3 FilipC (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\"><strong><br>Filip Cesar<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\">\r\n<p><img src=\"\/images\/215!215\/uzel\/0065404\/0055~~804sSS3KzEtU8MgsKs4vS1RwjnIFAA.jpg\" alt=\" \u25f3 Katerina Hirsova CZE (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\"><br><strong>Kate\u0159ina Hir\u0161ov\u00e1<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><strong><\/strong><\/p>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 79.2297%;\"><colgroup><col style=\"width: 54.9058%;\"><col style=\"width: 45.0697%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-style: none;\">\r\n<td>\r\n<h2>1<sup>st<\/sup> year:<br><br><\/h2>\r\n<\/td>\r\n<td><\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none;\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0018~~y0rMLk0CAA.jpg\" alt=\" \u25f3 jakub (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td><strong><br>Jakub Jan\u00e1\u010d<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none;\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0022~~y8ksy0wEAA.jpg\" alt=\" \u25f3 livia (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td><strong><br>L\u00edvia Platkov\u00e1<br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0004~~C_bxBwA.png\" alt=\" \u25f3 SLO (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none;\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0033~~c8nPTU4EAA.jpg\" alt=\" \u25f3 Domca (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td>\r\n<p><strong><br>Dominika Sousedov\u00e1<br><br><br><\/strong><strong><\/strong><\/p>\r\n<p><strong><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><span style=\"color: rgb(0, 173, 210); font-size: 19pt;\"><\/span><\/p>\r\n<p><span style=\"color: rgb(0, 173, 210); font-size: 19pt;\"><\/span><\/p>\r\n<p><span style=\"color: rgb(0, 173, 210); font-size: 19pt;\">Permanent Bachelor students:<\/span><\/p>\r\n<p><\/p>\r\n<p><\/p>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 72.1114%; height: 407.543px;\"><colgroup><col style=\"width: 60.1549%;\"><col style=\"width: 39.8377%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 48.5556px;\">\r\n<td style=\"height: 48.5556px;\">\r\n<h2><strong>3<sup>rd<\/sup> year:<\/strong><\/h2>\r\n<\/td>\r\n<td style=\"border-color: rgb(255, 255, 255); height: 48.5556px;\">\r\n<h2><strong>&nbsp;<\/strong><\/h2>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 147.181px;\">\r\n<td style=\"height: 147.181px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0046~~c8xLKUpNVPAAAA.jpg\" alt=\" \u25f3 Andrea H (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 147.181px;\"><strong><br>Andrea Hlad\u00edkov\u00e1<br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"height: 211.806px;\">\r\n<td style=\"height: 211.806px; border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0045~~c0xJzUlU8AYA.jpg\" alt=\" \u25f3 Adela K (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 211.806px; border-style: hidden;\"><strong><br>Ad\u00e9la Kova\u010di\u010dov\u00e1<br><br><br><\/strong><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" style=\"font-family: source_sans_probold; font-size: 16px; font-weight: 400; font-style: normal; color: rgb(51, 51, 51);\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><strong><\/strong><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<h2 class=\"MsoNormal\"><\/h2>\r\n<p><span style=\"color: rgb(0, 173, 210); font-size: 19pt;\"><br>Permanent High School students:<\/span><\/p>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 79.2297%; height: 154.083px;\"><colgroup><col style=\"width: 54.8704%;\"><col style=\"width: 45.0464%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-style: none; height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0009~~MzI1NYtPSjE2N9FNTizKT0nNystMTgUA.jpg\" alt=\" \u25f3 2556_bd374-carodejnice (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\"><strong><br>Ad\u00e9la Hanouskov\u00e1<br><\/strong><em>Gymn\u00e1zium Ji\u0159\u00edho z Pod\u011bbrad<\/em><strong><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0003~~c65KTc6ID0otKE3KyUzWKy5LBwA.png\" alt=\" \u25f3 Czech_Republic.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><br><\/strong><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><span style=\"color: rgb(0, 173, 210); font-size: 19pt;\"><\/span><\/p>\r\n<h2 class=\"MsoNormal\"><span style=\"mso-ansi-language: CS;\"><br>Visiting students and reserchers:<o:p><\/o:p><\/span><\/h2>\r\n<table style=\"border-collapse: collapse; width: 100%; height: 3339.74px;\" border=\"1\"><colgroup><col style=\"width: 30.6911%;\"><col style=\"width: 34.6943%;\"><col style=\"width: 34.4891%;\"><\/colgroup>\r\n<tbody>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 26px;\">\r\n<td style=\"height: 26px;\"><\/td>\r\n<td style=\"height: 26px; text-align: center;\">\r\n<h2 style=\"text-align: center;\">2022<\/h2>\r\n<\/td>\r\n<td style=\"height: 26px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0017~~S87ITCxKBAA.jpg\" alt=\" \u25f3 chiara (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p class=\"MsoNormal\"><span style=\"mso-ansi-language: CS;\"><strong><br>Chiara Siguri, MSc<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><br><o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"mso-ansi-language: CS;\"><\/span><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\"><br><br><strong>University of Cagliari<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0011~~S8xJLS7OTAQA.jpg\" alt=\" \u25f3 alessia (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\"><strong><br>Alessia Onali. MSc<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/td>\r\n<td style=\"height: 154.083px;\"><br><strong><br>University of Cagliari<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0026~~K04sSswAAA.jpg\" alt=\" \u25f3 sarah (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\"><br><strong>Sarah Van Den Bussche<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/td>\r\n<td style=\"height: 154.083px;\"><br><br><strong>University of Poitiers<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0014~~S07MzczJSQUA.jpg\" alt=\" \u25f3 camille (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\"><br><strong>Camille Devilliers<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/td>\r\n<td style=\"height: 154.083px;\"><br><br><strong>University of Poitiers<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 26px;\">\r\n<td style=\"height: 26px;\"><\/td>\r\n<td style=\"height: 26px;\">\r\n<h2 style=\"text-align: center;\">2023<\/h2>\r\n<\/td>\r\n<td style=\"height: 26px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0023~~y00sykzMSwQA.jpg\" alt=\" \u25f3 mariana (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><\/p>\r\n<p style=\"text-align: left;\"><strong><br>Marianna Bufano, PhD<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\"><br><br><strong>University of Rome<\/strong><br><strong> \u201eLa Sapienza\u201c<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0015~~Sy9KTQcA.jpg\" alt=\" \u25f3 greg (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Gregory Mathez, MSc<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0006~~c_YAAA.png\" alt=\" \u25f3 CH (png) \u2192 (origin\u00e1l)\" width=\"35\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\"><br><br><br><strong>Centre Hospitalier Universitaire Vaudois, Lausanne<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0025~~y83MSc1LBAA.jpg\" alt=\" \u25f3 milena (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Milena Nicolosi, MSc<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\"><br><br><br><strong>University of Catania<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0024~~y81MzkjNyUkFAA.jpg\" alt=\" \u25f3 michelle (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong><span style=\"font-size: 11.0pt; line-height: 107%; font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-font-family: Arial; mso-bidi-theme-font: minor-bidi; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Michelle Femi Agbetuyi<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0008~~c8tJTI_PT4v3LErNScxL0SsuSwcA.png\" alt=\" \u25f3 Flag_of_Ireland.svg (png) \u2192 (origin\u00e1l)\" width=\"70\" height=\"35\"><br><\/span><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><br><br><br><strong>Universit\u00e9 Bourgogne <\/strong><\/p>\r\n<p><strong>Franche-Comt\u00e9<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-color: rgb(255, 255, 255); height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0013~~SyxKzshMBQA.jpg\" alt=\" \u25f3 archie (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Archie McCulloch<br><br><br><\/strong><img src=\"\/images\/0!0\/uzel\/0065404\/0007~~c3cCAA.png\" alt=\" \u25f3 GB (png) \u2192 (origin\u00e1l)\" width=\"70\" height=\"35\"><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\"><br><br><br><strong>high school student<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px; border-style: none;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0034~~S8_ML0vMSwQA.jpg\" alt=\" \u25f3 giovana (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><strong><br>Giovanna Pitasi<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University of Messina<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none;\">\r\n<td><img src=\"\/images\/215!215\/uzel\/0065404\/0056~~c0osSsxTcExJLFJwScxJz0xWCAkNAgA.jpg\" alt=\" \u25f3 Baran Adar Dalgic TUR (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td>\r\n<p style=\"text-align: left;\"><br><br><strong>Baran Adar Dalg\u0131\u00e7<br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0041~~Kyktyk6tBAA.png\" alt=\" \u25f3 turkey (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"36\"><\/strong><\/p>\r\n<\/td>\r\n<td>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none; height: 26px;\">\r\n<td style=\"height: 26px;\"><\/td>\r\n<td style=\"height: 26px;\">\r\n<h2 style=\"text-align: center;\">2024<\/h2>\r\n<\/td>\r\n<td style=\"height: 26px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none; height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0035~~K8nIz00sBgA.jpg\" alt=\" \u25f3 thomas (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><strong><br>Thomas Suau<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University of Poitiers<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none; height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0036~~SywqySgtAgA.jpg\" alt=\" \u25f3 arthur (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Arthur Demoute<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><strong><br><br><br>University of Poitiers<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none; height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0037~~K87PycxLBQA.jpg\" alt=\" \u25f3 soline (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Soline Brossard<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University of Poitiers<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"border-style: none; height: 154.083px;\">\r\n<td style=\"height: 154.083px;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0038~~S8tMy8ypBAA.jpg\" alt=\" \u25f3 fifily (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Daniele Aiello<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"height: 154.083px;\">\r\n<p><br><br><br><strong>University of Modena<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0047~~800sSc1S8AYA.jpg\" alt=\" \u25f3 Matej K (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Mat\u011bj Kereke\u0161<br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0004~~C_bxBwA.png\" alt=\" \u25f3 SLO (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 26px;\">\r\n<td style=\"border-style: hidden; height: 26px;\"><\/td>\r\n<td style=\"border-style: hidden; height: 26px;\">\r\n<h2 style=\"text-align: center;\">2025<\/h2>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 26px;\">\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0051~~88rPSMwDAA.jpg\" alt=\" \u25f3 Johan (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Johan Filoche<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>National College of Chemical Engineering (ENSCMu)<br><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0053~~80ssSczJTAQA.jpg\" alt=\" \u25f3 Natalia (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Natalia Del Rio<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0054~~c8tJTI_PT4sPLkjMzNMrLksHAA.png\" alt=\" \u25f3 Flag_of_Spain.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>Institute of Medicinal Chemistry (IQM-CSIC)<br><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0050~~c0ssSswAAA.jpg\" alt=\" \u25f3 Farah (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Farah Baudry<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University of Poitiers<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0052~~88kvzSxOBAA.jpg\" alt=\" \u25f3 Louisa (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Louisa Meissner<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University of Poitiers<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 154.083px;\">\r\n<td style=\"border-style: hidden; height: 154.083px;\">&nbsp; <img src=\"\/images\/215!215\/uzel\/0065404\/0049~~c8wryc_LzAcA.jpg\" alt=\" \u25f3 Antonio (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Antonio Curcio<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden; height: 154.083px;\">\r\n<p><\/p>\r\n<p><strong><br><br><br>University Magna Graecia of Catanzaro<br><\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0057~~c0ksy0xJVQjLzM9JzCtJVfAMcQQA.jpg\" alt=\" \u25f3 Davide Violante ITA (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Davide Violante<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0002~~8yxJzKnUKy5LBwA.png\" alt=\" \u25f3 Italy.svg (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p><br><br><br><strong>Universita' degli Studi del Piemonte Orientale<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0058~~C8lMVHDNKS7JL1dw9XMHAA.jpg\" alt=\" \u25f3 Tia Elstow ENG (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Tia Elstow&nbsp;<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0007~~c3cCAA.png\" alt=\" \u25f3 GB (png) \u2192 (origin\u00e1l)\" width=\"70\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p><br><br><br><strong>Cardiff University<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0059~~803MSytKTVFwKsrMy04tUnB3DQIA.jpg\" alt=\" \u25f3 Manfred Brinker GER (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Manfred Brinker<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0060~~c08tyk3Mq9R1y0lMBwA.jpg\" alt=\" \u25f3 Germany-Flag (jpg) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p><br><br><br><strong>Heidelberg University&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"border-style: hidden;\"><img src=\"\/images\/215!215\/uzel\/0065404\/0061~~c8xNzclMVQhOzE0sSlFwC3IEAA.jpg\" alt=\" \u25f3 Amelie Samard FRA (jpg) \u2192 (o\u0159ez 215*215px)\" width=\"150\" height=\"150\"><\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p style=\"text-align: left;\"><br><br><strong>Am\u00e9lie Samard<br><br><br><img src=\"\/images\/0!0\/uzel\/0065404\/0005~~cwsCAA.png\" alt=\" \u25f3 FR (png) \u2192 (origin\u00e1l)\" width=\"53\" height=\"35\"><\/strong><\/p>\r\n<\/td>\r\n<td style=\"border-style: hidden;\">\r\n<p><br><br><br><strong>\u00c9cole Nationale de Chimie de Mulhouse<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["65402","72792"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"65402":{"idvazba":"167910","nad_uzel":"136561","pod_uzel":"65402","url":"","sablona":"4","nazev":"Brancale Research Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:03:00","platne_do":null,"iduzel":"65402","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"72792":{"idvazba":"167911","nad_uzel":"136561","pod_uzel":"72792","url":"","sablona":"20","nazev":"Slider Br","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"22.08.2023 14:48:01.600895","platne_do":null,"iduzel":"72792","obsah":null,"class":"slider","autonomni":"0","pod_uzly":["72794"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"72794":{"idvazba":"89036","nad_uzel":"72792","pod_uzel":"72794","url":"","sablona":"20","nazev":"Brancale","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:10:00","platne_do":null,"iduzel":"72794","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:28:\"0004~~808qOrywKjXbwMAQAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"sm\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136560":{"idvazba":"167906","nad_uzel":"136559","pod_uzel":"136560","url":"\/research\/brancale\/research_clone_85743","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/brancale\/research_clone_85743}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 11:08:00","platne_do":null,"iduzel":"136560","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:2560:\"<h2 class=\"MsoNormal\"><b><span lang=\"EN-GB\">Research projects:<\/span><\/b><\/h2>\r\n<p><b><span lang=\"EN-GB\"><\/span><\/b><\/p>\r\n<p class=\"MsoNormal\"><b><span lang=\"EN-GB\">RNA-binding agents as antiviral compounds<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\">In this project we aim to design and synthesise a series of new small molecules with drug-like properties, that are able to selectively bind to viral RNA, blocking viral replication.<o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><b><span lang=\"EN-GB\">Protein degraders as antivirals<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\">The main goal of this project is to prepare novel PROTACs compounds that are able to promote the degradation of viral proteins by the natural cellular mechanisms.<o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><b><span lang=\"EN-GB\">Modulators of mitochondria dynamics<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\">Mitochondrial disfunctions are responsible for different diseases. In our group we are working on compounds that affect mitochondria dynamics. These molecules are potentially useful against cancer and other therapeutic areas.<o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><b><span lang=\"EN-GB\">Novel antiviral compounds against Flaviviridae<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\">This project is focused on the optimization of the previously identified hit compounds showing activity against Flaviviruses (e.g., Dengue, Zika).<o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><b><span lang=\"EN-GB\">From natural compounds to small, drug-like molecules <o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span lang=\"EN-GB\">Natural compounds are a good source of bioactive compounds. However, they are often not developed as drugs. In this project we are designing drug-like analogues of a natural compound with neuroprotective activity.<o:p><\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-GB\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-US\" style=\"mso-ansi-language: EN-US;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-US\" style=\"mso-ansi-language: EN-US;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-US\" style=\"mso-ansi-language: EN-US;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p class=\"MsoNormal\"><span lang=\"EN-US\" style=\"mso-ansi-language: EN-US;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["65402","72792"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"65402":{"idvazba":"167910","nad_uzel":"136561","pod_uzel":"65402","url":"","sablona":"4","nazev":"Brancale Research Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:03:00","platne_do":null,"iduzel":"65402","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"72792":{"idvazba":"167911","nad_uzel":"136561","pod_uzel":"72792","url":"","sablona":"20","nazev":"Slider Br","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"22.08.2023 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11:10:00","platne_do":null,"iduzel":"72794","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:28:\"0004~~808qOrywKjXbwMAQAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"sm\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136561":{"idvazba":"167909","nad_uzel":"136559","pod_uzel":"136561","url":"\/research\/brancale\/publications_clone_44619","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/brancale\/publications_clone_44619}","poradi":"4","skupina_www":"everyone","platne_od":"12.05.2026 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department\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["116954","116955","116956"],"poduzly_count":3,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"116954":{"idvazba":"144434","nad_uzel":"116997","pod_uzel":"116954","url":"","sablona":"52","nazev":"2025","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.12.2025 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13:58:00","platne_do":null,"iduzel":"116956","class":"accordion","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136669":{"idvazba":"168158","nad_uzel":"116995","pod_uzel":"136669","url":"\/research\/cibulka","sablona":"58","nazev":"Cibulka","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka}","poradi":"3","skupina_www":"everyone","platne_od":"29.09.2026 19:46:00","platne_do":null,"iduzel":"136669","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:7:\"Cibulka\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:10806:\"<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136669\/0067~~K87JTEktUkjOTCrNyU5USM0DAA.png\" alt=\" \u25f3 slider cibulka en (png) \u2192 (origin\u00e1l)\" width=\"833\" height=\"203\"><\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136669\/0069~~C84uLcjMS1QwMjAyBQA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Skupina 2025 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"227\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136669\/0074~~c3IJ9nA2MjAyAwA.png\" alt=\" \u25f3 BDSHC2026 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"152\"><\/p>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136669\/0075~~c3IJ9nCONzIwMnMEAA.png\" alt=\" \u25f3 BDSHC_2026A (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"867\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136669\/0073~~80stL443tAQA.jpg\" alt=\" \u25f3 News_19 (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0066~~C0tNzixKzVYwMjAyBQA.png\" alt=\" \u25f3 Vecirek 2025 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/images\/0!0\/uzel\/0136669\/0070~~CyhKrUrNK0lMTk1PTC4yMjAy003NSwcA.png\" alt=\" \u25f3 Prezentacegacr2026-eng (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0060~~cw32d1YwMjAyBQA.png\" class=\"img_fancy_no\" alt=\" \u25f3 ESOC 2025 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"250\"><img src=\"\/files\/uzel\/0136669\/0059~~Sy3OTzYyMDLVzclPzwcA.png\" class=\"img_float_right img_fancy_no\" alt=\" \u25f3 esoc2025-logo (png) \u2192 (origin\u00e1l)\" width=\"88\" height=\"100\"><\/p>\r\n<p style=\"text-align: right;\" class=\"subTitle\"><\/p>\r\n<p style=\"text-align: left;\" class=\"subTitle\">Lecture: R. Cibulka<br>Poster: T. Pavlovska, J.Semeck\u00fd, R. Sponar, E. Svobodov\u00e1, I. Weisheitelov\u00e1 a E. Zubova<\/p>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><\/p>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0062~~Sy3OTzYyMDLVzU8qMgQA.png\" alt=\" \u25f3 esoc2025-obr1 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"481\"><\/p>\r\n<p style=\"text-align: right;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0061~~c84vSM3LSExPzVMIzcssSy0qziypBAA.png\" alt=\" \u25f3 Copenhagen University (png) \u2192 (origin\u00e1l)\" width=\"268\" height=\"100\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0058~~883MyS-rVDAyMDIFAA.png\" alt=\" \u25f3 Milovy 2025 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/images\/0!0\/uzel\/0136669\/0070~~80stL443tAAA.jpg\" alt=\" \u25f3 News_18 (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0057~~C67MLcgvzizNVcjPU3BOLEnMqSzOLFYwMjAyAQA.png\" alt=\" \u25f3 Symposium of Catalysis 2024 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/p>\r\n<p><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0058~~cyzJScwrSVQwMjAyAQA.png\" alt=\" \u25f3 Atlanta 2024 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/p>\r\n<hr>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0054~~883MyS-rjDcyMDIBAA.png\" alt=\" \u25f3 Milovy_2024 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"177\"><\/p>\r\n<p style=\"text-align: justify;\"><span jsaction=\"agoMJf:PFBcW;MZfLnc:P7O7bd;nt4Alf:pvnm0e,pfE8Hb,PFBcW;B01qod:dJXsye;H1e5u:iXtTIf;lYIUJf:hij5Wb\" jsname=\"txFAF\" class=\"jCAhz ChMk0b\" jscontroller=\"BiTO4b\"><span class=\"ryNqvb\" jsname=\"W297wb\" jsaction=\"click:E6Tfl,ogZjnb,qlVvte;contextmenu:Nqw7Te,QP7LD; mouseout:Nqw7Te; mouseover:E6Tfl,c2aHje\">V roce 2024 \u010cesk\u00e1 spole\u010dnost chemick\u00e1 a \u010cesk\u00e1 spole\u010dnost pro biochemii a molekul\u00e1rn\u00ed biologii ve spolupr\u00e1ci s gener\u00e1ln\u00edm partnerem Merck Life Science spol.<\/span><\/span><span> <\/span><span jsaction=\"agoMJf:PFBcW;MZfLnc:P7O7bd;nt4Alf:pvnm0e,pfE8Hb,PFBcW;B01qod:dJXsye;H1e5u:iXtTIf;lYIUJf:hij5Wb\" jsname=\"txFAF\" class=\"jCAhz ChMk0b\" jscontroller=\"BiTO4b\"><span class=\"ryNqvb\" jsname=\"W297wb\" jsaction=\"click:E6Tfl,ogZjnb,qlVvte;contextmenu:Nqw7Te,QP7LD; mouseout:Nqw7Te; mouseover:E6Tfl,c2aHje\">s.r.o.<\/span><\/span><span> <\/span><span jsaction=\"agoMJf:PFBcW;MZfLnc:P7O7bd;nt4Alf:pvnm0e,pfE8Hb,PFBcW;B01qod:dJXsye;H1e5u:iXtTIf;lYIUJf:hij5Wb\" jsname=\"txFAF\" class=\"jCAhz ChMk0b\" jscontroller=\"BiTO4b\"><span class=\"ryNqvb\" jsname=\"W297wb\" jsaction=\"click:E6Tfl,ogZjnb,qlVvte;contextmenu:Nqw7Te,QP7LD; mouseout:Nqw7Te; mouseover:E6Tfl,c2aHje\">(www.sigmaaldrich.cz) a dal\u0161\u00edmi sponzory ji\u017e tradi\u010dn\u011b po\u0159\u00e1d\u00e1 Mezioborov\u00e9 setk\u00e1n\u00ed mlad\u00fdch v\u011bdc\u016f a student\u016f z chemie, biochemie, molekul\u00e1rn\u00ed biologie a biomateri\u00e1lov\u00fdch obor\u016f. Na\u0161i pracovn\u00ed skupinu na tomto setk\u00e1n\u00ed zastupoval Ing. Rostislav Sponar.<\/span><\/span><\/p>\r\n<p style=\"text-align: right;\"><span jsaction=\"agoMJf:PFBcW;MZfLnc:P7O7bd;nt4Alf:pvnm0e,pfE8Hb,PFBcW;B01qod:dJXsye;H1e5u:iXtTIf;lYIUJf:hij5Wb\" jsname=\"txFAF\" class=\"jCAhz ChMk0b\" jscontroller=\"BiTO4b\"><span class=\"ryNqvb\" jsname=\"W297wb\" jsaction=\"click:E6Tfl,ogZjnb,qlVvte;contextmenu:Nqw7Te,QP7LD; mouseout:Nqw7Te; mouseover:E6Tfl,c2aHje\"><a href=\"http:\/\/www.interdisciplinarymeeting.cz\/\" target=\"_blank\" rel=\"noopener\">XXIII. Interdisciplinary meeting of young life scientists<\/a><br><\/span><\/span><\/p>\r\n<p style=\"text-align: center;\"><span jsaction=\"agoMJf:PFBcW;MZfLnc:P7O7bd;nt4Alf:pvnm0e,pfE8Hb,PFBcW;B01qod:dJXsye;H1e5u:iXtTIf;lYIUJf:hij5Wb\" jsname=\"txFAF\" class=\"jCAhz ChMk0b\" jscontroller=\"BiTO4b\"><span class=\"ryNqvb\" jsname=\"W297wb\" jsaction=\"click:E6Tfl,ogZjnb,qlVvte;contextmenu:Nqw7Te,QP7LD; mouseout:Nqw7Te; mouseover:E6Tfl,c2aHje\"><img src=\"\/files\/uzel\/0136669\/0055~~883MyS-rjDcyMDKJdwQA.png\" class=\"img_fancy_no\" alt=\" \u25f3 Milovy_2024_A (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"347\"><\/span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"subTitle\" style=\"text-align: left;\"><img src=\"\/images\/0!0\/uzel\/0136669\/0071~~80stL443NAcA.jpg\" alt=\" \u25f3 News_17 (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/h2>\r\n<hr>\r\n<h2 class=\"subTitle\" style=\"text-align: left;\"><\/h2>\r\n<p><span class=\"cervena0\"><img src=\"\/files\/uzel\/0136669\/0052~~889JTAMA.png\" alt=\" \u25f3 Olaf (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"372\"><\/span><\/p>\r\n<p style=\"text-align: right;\"><span class=\"cervena0\"><a href=\"\/files\/uzel\/0136669\/0051~~889JTFN41DBZITexODm_RCE_TcGjMiVVISCxKBsA.pptx\" target=\"_blank\" rel=\"noopener\">Olaf \u2013 mascot of Hyde Park<\/a><\/span><\/p>\r\n<p><span class=\"cervena0\"><span class=\"cerna0\"><\/span><\/span><\/p>\r\n<hr>\r\n<h2><span class=\"cervena0\">Cena ministra \u0161kolstv\u00ed, ml\u00e1de\u017ee a t\u011blov\u00fdchovy za vynikaj\u00edc\u00ed vzd\u011bl\u00e1vac\u00ed \u010dinnost na vysok\u00e9 \u0161kole<\/span><\/h2>\r\n<p style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0049~~c85MKs3JToxPTs1LBAA.png\" alt=\" \u25f3 Cibulka_cena (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<p style=\"text-align: right;\"><a href=\"https:\/\/www.msmt.cz\/ministerstvo\/novinar\/tiskove-zpravy\" target=\"_blank\" rel=\"noopener\">ministerstvo\/novinar\/tiskove-zpravy<\/a><\/p>\r\n<hr>\r\n<h2 class=\"subTitle\" style=\"text-align: left;\"><span class=\"cervena0\">Studentsk\u00e1 cena Vitriol 2023<\/span><\/h2>\r\n<p style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0047~~C8ssKcrMz4k3MjAyBgA.png\" alt=\" \u25f3 Vitriol_2023 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/p>\r\n<p style=\"text-align: right;\"><a href=\"https:\/\/aktivni.vscht.cz\/studentska-cena-vitriol\" target=\"_blank\" rel=\"noopener\">Vitriol - cena student\u016f V\u0160CHT Praha<\/a><\/p>\r\n<hr>\r\n<h2 class=\"subTitle\" style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0045~~88lMyslMTjUyMDIGAA.png\" alt=\" \u25f3 Liblice2023 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"118\"><\/h2>\r\n<h3 style=\"text-align: center;\"><strong>Ivana Weisheitelov\u00e1 z\u00edskala na konferenci Liblice cenu za nejlep\u0161\u00ed poster<\/strong><\/h3>\r\n<p style=\"text-align: center;\"><strong><img src=\"\/files\/uzel\/0136669\/0046~~8yxLBAA.png\" alt=\" \u25f3 Iva (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/strong><\/p>\r\n<p style=\"text-align: center;\"><strong><img src=\"\/files\/uzel\/0136669\/0049~~88lMyslMTjUyMDKONwQA.png\" alt=\" \u25f3 Liblice2023_1 (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/strong><\/p>\r\n<hr>\r\n<h2 style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: center; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\"><span class=\"modra0\">8th International Conference on Multicomponent Reactions and Related Chemistry<\/span><\/span><\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\"><span class=\"modra0\">September 6th to 8th 2023 in Burgos, Spain<\/span><\/span><\/p>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\"><span class=\"modra0\"><img src=\"\/files\/uzel\/0136669\/0050~~C0gsy8kvK85OjA8uSMzMAwA.png\" alt=\" \u25f3 Pavlovska_Spain (png) \u2192 (origin\u00e1l)\" width=\"650\" height=\"488\"><\/span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"subTitle\" style=\"text-align: center;\">ESOC 2023, 22nd European Symposium on Organic Chemistry, <i class=\"fa fa-map-marker\"><\/i>Ghent, Belgium, July 9-13, 2023<\/h2>\r\n<p class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0042~~MzQzsLQwMzU0tgzITC4pLUqNd0rMy0stivcJ0jU0MzDQNTcy0C3PLMkISa0oAQA.jpg\" class=\"img_fancy_no\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 1609865139Picture_Banner_LR-1600-720-withText (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"293\"><\/p>\r\n<p style=\"text-align: center;\" class=\"subTitle\"><img src=\"\/files\/uzel\/0136669\/0043~~c89IzSsxBAA.jpg\" alt=\" \u25f3 Ghent1 (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/p>\r\n<p style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136669\/0044~~c89IzStRMAIA.jpg\" alt=\" \u25f3 Ghent 2 (jpg) \u2192 (origin\u00e1l)\" width=\"650\" height=\"366\"><\/p>\r\n<p><\/p>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 100%; height: 53.1905px;\">\r\n<tbody>\r\n<tr style=\"height: 17.1905px;\">\r\n<td style=\"width: 33.3333%; text-align: center; height: 17.1905px;\"><\/td>\r\n<td style=\"width: 33.3333%; text-align: center; height: 17.1905px;\"><\/td>\r\n<td style=\"width: 33.3333%; text-align: center; height: 17.1905px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 36px;\">\r\n<td style=\"width: 33.3333%; text-align: center; height: 36px;\"><\/td>\r\n<td style=\"width: 33.3333%; text-align: center; height: 36px;\">\r\n<p><\/p>\r\n<p><\/p>\r\n<\/td>\r\n<td style=\"width: 33.3333%; text-align: center; height: 36px;\"><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><\/p>\r\n<p style=\"text-align: right;\">&nbsp;<a href=\"http:\/\/uoch.vscht.cz\/vedecke-skupiny\/cibulka\/19347\" class=\"jstree-anchor jstree-hovered\">Archiv novinky&nbsp;<\/a><\/p>\r\n<p style=\"text-align: right;\"><a href=\"http:\/\/uoch.vscht.cz\/vedecke-skupiny\/cibulka\/16420\" class=\"jstree-anchor jstree-hovered\">Archiv&nbsp;foto <\/a><\/p>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["136670","142446","136672","136673","15408","136675","136676","136677","136681","136684","136687","136694","136702"],"poduzly_count":13,"poduzly_count_aut":10,"poduzly":{"poduzly_count_aut_sum":6,"136670":{"idvazba":"168103","nad_uzel":"136669","pod_uzel":"136670","url":"\/research\/cibulka\/136670","sablona":"39","nazev":"Archiv foto","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/136670}","poradi":"0","skupina_www":"everyone","platne_od":"13.05.2026 07:57:10.176803","platne_do":null,"iduzel":"136670","obsah":"a:9:{s:5:\"nazev\";s:11:\"Archiv foto\";s:9:\"seo_title\";s:11:\"Archiv foto\";s:8:\"seo_desc\";s:11:\"Archiv foto\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka_galerie_velka","autonomni":"1","pod_uzly":["136671"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"136671":{"idvazba":"168104","nad_uzel":"136670","pod_uzel":"136671","url":"","sablona":"11","nazev":"Foto z laborato\u0159e","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"13.05.2026 07:57:10.218437","platne_do":null,"iduzel":"136671","obsah":"a:1:{s:6:\"nadpis\";s:4:\"Foto\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"142446":{"idvazba":"175437","nad_uzel":"136669","pod_uzel":"142446","url":"\/research\/cibulka\/galerie","sablona":"49","nazev":"Gallery","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/galerie}","poradi":"1","skupina_www":"everyone","platne_od":"20.07.2026 15:35:00","platne_do":null,"iduzel":"142446","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:7:\"Gallery\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["142691","142690","142694","142696","142695","136703","142447"],"poduzly_count":7,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"142691":{"idvazba":"175791","nad_uzel":"142446","pod_uzel":"142691","url":"","sablona":"47","nazev":"Mezikecy1","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"20.07.2026 15:35:00","platne_do":null,"iduzel":"142691","obsah":"a:4:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:4:\"bila\";s:4:\"text\";s:12:\"<p>Staff<\/p>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"142690":{"idvazba":"175790","nad_uzel":"142446","pod_uzel":"142690","url":"","sablona":"11","nazev":"Galerie zam\u011bstnanci","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"20.07.2026 15:13:00","platne_do":null,"iduzel":"142690","obsah":"a:4:{s:6:\"nadpis\";s:0:\"\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"142694":{"idvazba":"175794","nad_uzel":"142446","pod_uzel":"142694","url":"","sablona":"47","nazev":"Mezikecy2","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"20.07.2026 15:36:00","platne_do":null,"iduzel":"142694","obsah":"a:4:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:4:\"bila\";s:4:\"text\";s:21:\"<p>Ph.D. Students<\/p>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"142696":{"idvazba":"175796","nad_uzel":"142446","pod_uzel":"142696","url":"","sablona":"11","nazev":"Ph.D. studenti","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"20.07.2026 15:36:00","platne_do":null,"iduzel":"142696","obsah":"a:4:{s:6:\"nadpis\";s:0:\"\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"142695":{"idvazba":"175795","nad_uzel":"142446","pod_uzel":"142695","url":"","sablona":"47","nazev":"Mezykecy3","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"20.07.2026 15:36:00","platne_do":null,"iduzel":"142695","obsah":"a:4:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:4:\"bila\";s:4:\"text\";s:59:\"<p>Photos from prehistory and history of research group<\/p>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136703":{"idvazba":"175436","nad_uzel":"142446","pod_uzel":"136703","url":"","sablona":"11","nazev":"Galerie absolventi","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"20.07.2026 15:36:00","platne_do":null,"iduzel":"136703","obsah":"a:4:{s:6:\"nadpis\";s:0:\"\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"142447":{"idvazba":"175438","nad_uzel":"142446","pod_uzel":"142447","url":"","sablona":"47","nazev":"Mezikecy","_url_prefix":null,"poradi":"6","skupina_www":"everyone","platne_od":"13.07.2026 12:45:00","platne_do":null,"iduzel":"142447","obsah":"a:4:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:4:\"bila\";s:4:\"text\";s:49:\"<p>And now for something completely different<\/p>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136672":{"idvazba":"168105","nad_uzel":"136669","pod_uzel":"136672","url":"\/research\/cibulka\/136672","sablona":"49","nazev":"V\u011bdeck\u00e9 skupiny","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/136672}","poradi":"2","skupina_www":"everyone","platne_od":"13.05.2026 07:57:10.540152","platne_do":null,"iduzel":"136672","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:17:\"V\u011bdeck\u00e9 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07:57:10.886971","platne_do":null,"iduzel":"136676","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136677":{"idvazba":"170791","nad_uzel":"136669","pod_uzel":"136677","url":"\/research\/cibulka\/Vyzkum","sablona":"58","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/Vyzkum}","poradi":"7","skupina_www":"everyone","platne_od":"15.07.2026 15:54:00","platne_do":null,"iduzel":"136677","obsah":"a:13:{s:5:\"nazev\";s:8:\"Research\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:33:\"0012~~K87JTEktUiirrMouzVUwBAA.png\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:32140:\"<h2 class=\"article_header-title\" style=\"text-align: center;\" tabindex=\"0\"><span class=\"hlFld-Title\" property=\"headline\">Electrochemistry Facilitates the Chemoselectivity of Benzylic Alcohol Oxidations Mediated by Flavin-Based Photoredox Catalysis<\/span><\/h2>\r\n<p style=\"text-align: center;\" class=\"citation__title\"><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.5c04603\" target=\"_blank\" rel=\"noopener\">doi.org\/10.1021\/acs.orglett.5c04603<\/a><\/p>\r\n<p style=\"text-align: left;\" class=\"citation__title\">Abstract:<\/p>\r\n<p style=\"text-align: justify;\" class=\"citation__title\"><span><img src=\"\/images\/0!0\/uzel\/0136677\/0013~~y8xNTE8tjs9NTckszY3PzzFNNjAxMzCONzAwMAMA.gif\" class=\"img_float_right img_fancy_no\" alt=\" \u25f3 images_medium_ol5c04603_0006 (gif) \u2192 (origin\u00e1l)\" width=\"300\" height=\"116\">The use of oxygen for catalyst regeneration in photoredox catalysis causes selectivity problems, because the generation of reactive oxygen species initiates overoxidations and side oxidations. Herein, we present a system using the electrochemical regeneration of a flavin catalyst under inert conditions. Our process allows the chemoselective oxidation of primary and secondary benzylic alcohols to carbonyl compounds without unwanted overoxidation to carboxylic acids. The method tolerates other oxidation-sensitive groups such as methyl, methylsulfanyl, or pinacolboryl groups.<\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Deazaalloxazines \u2013 Flavin Derivatives That Provide Reductive Photoredox Catalysis with Inert Substrates<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1002\/chem.202502897\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.202502897<\/a><\/p>\r\n<p>Abstract:<\/p>\r\n<p style=\"text-align: justify;\"><span>Reductive transformations of substances that are difficult to reduce continue to pose challenges for photoredox catalysis. Promising photoreduction catalysts include flavin and deazaflavin derivatives; however, even their reductive abilities are limited for the range of substrates considered \u201cinert\u201d. In this work, we present 5-deazaalloxazines, a new group of deazaflavin analogues that are predisposed to catalyze reductions due to their low reduction potential (down to \u22121.65&nbsp;V vs. SCE) even in the ground state. We studied three series of 5-deazaalloxazines ([i] 5-unsubstituted, [ii] 5-aryldeazaalloxazines, and [iii] 5-trifluoromethyl-5-deazaalloxazines) to determine their photophysical and electrochemical properties and their ability to participate in model photoreduction reactions. From 31 compounds, we selected 1,3-dimethyl-7,8-dimethoxy-5-(<\/span><i>o<\/i><span>-tolyl)-5-deazaalloxazine [<\/span><b>3a(<i>o<\/i>-MePh)<\/b><span>], as it showed, among other things, the highest efficiency in photodehalogenation of&nbsp;<\/span><i>p<\/i><span>-fluoroanisole and was photostable and absorbed in the visible light region, thereby allowing photoreactions using a 400&nbsp;nm LED. Practical applicability was demonstrated in the C\u2500P coupling reaction of electron-rich aryl halides (including chloroanisoles and&nbsp;<\/span><i>p<\/i><span>-fluoroanisole) with trimethyl phosphite, providing an arylation reaction to form dimethyl arylphosphonates, and in the release\/deprotection of amines from the corresponding tosyl and triflylamides.<\/span><\/p>\r\n<p style=\"text-align: center;\" class=\"Head u-font-serif u-h2 u-margin-s-ver\"><img src=\"\/images\/0!0\/uzel\/0136677\/0011~~MwQA.png\" alt=\" \u25f3 1 (png) \u2192 (origin\u00e1l)\" width=\"400\" height=\"225\"><\/p>\r\n<p style=\"text-align: justify;\" class=\"Head u-font-serif u-h2 u-margin-s-ver\"><span class=\"title-text\"><span>7,8-Dimethoxy-5-aryl-5-deazaalloxazines (<\/span><b>dAll<\/b><span>) are new class of photostable, visible-light-absorbing flavin derivatives which are strongly reducible upon excitation with 400&nbsp;nm light. It was demonstrated on difficult-to-reduce aryl halides like bromo-, chloro- and fluoroanisoles which were transformed to phosphonates by reductive cross-coupling with trimethyl phosphite or on desulfonylation of sulfonamides to free amines by S\u2500N bond cleavage.<\/span><\/span><\/p>\r\n<hr>\r\n<h2 id=\"screen-reader-main-title\" class=\"Head u-font-serif u-h2 u-margin-s-ver\" style=\"text-align: center;\"><span class=\"title-text\">Redox properties of flavin derivatives: A comparative study<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"title-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2025.147520\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.electacta.2025.147520<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"title-text\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"title-text\"><span>Flavins as cofactors in natural systems as well as their artificial analogues used in catalysis are unique due to their specific redox properties. Our study provides the first direct comparison of the electrochemical behavior of various flavin derivatives: in addition to derivatives of the natural flavins possessing isoalloxazine structure, the experiments were oriented also to their analogues: alloxazines, deazaflavins and flavinium or deazaflavinium salts. We focused on the redox properties of six series of the mentioned flavin types with the stress on the substitution in positions 7 and 8 in connection with the structure of the core using various solvents and electrode materials. In addition to the study by cyclic and rotating disk voltammetry (CV and RDV), we turned our attention on the&nbsp;<\/span><em>in-situ<\/em><span>&nbsp;measurements of EPR spectra of radicals generated electrochemically. Experiments are accompanied by theoretical treatment enabling interpretation of electrochemical data and prediction of redox potential values of newly designed flavin derivatives.<\/span><\/span><\/p>\r\n<p><span class=\"title-text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"c-article-title\" data-test=\"article-title\" style=\"text-align: center;\">Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1038\/s41467-025-63233-4\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41467-025-63233-4<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\"><img src=\"\/images\/0!0\/uzel\/0136677\/0010~~C04GAA.png\" class=\"img_float_right\" alt=\" \u25f3 Sc (png) \u2192 (origin\u00e1l)\" width=\"300\" height=\"300\">Abstract:<\/p>\r\n<p style=\"text-align: justify;\"><span>In recent years, the catalytic activity of scandium triflate Sc(OTf)<\/span><sub>3<\/sub><span>&nbsp;has attracted significant attention due to its robust Lewis acidity and the oxophilicity of Sc<\/span><sup>3+<\/sup><span>. These features have led to impressive progress in developing diverse organic reactions, including C-C bond formation. The Sc<\/span><sup>3+<\/sup><span>&nbsp;also facilitates single electron transfer in photoinduced reactions either by coordination to an organophotoredox catalyst, which modifies its redox reactivity, or by the formation of a scandium\u2013superoxide anion complex after electron transfer from a light-absorbing redox-active compound. The prior consideration of Sc<\/span><sup>3+<\/sup><span>&nbsp;as a redox-inactive\/innocent metal ion initially hampered the investigation of the possibility of using Sc(OTf)<\/span><sub>3<\/sub><span>&nbsp;as a sole visible light photoredox catalyst. This work demonstrates the use of Sc(OTf)<\/span><sub>3<\/sub><span> as a visible light photocatalyst capable of direct and mild aerobic oxidative C-H functionalisation of aromatic substrates by oxidation of the benzylic position and direct cyanation of the aromatic ring.<\/span><span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Deazaflavin-Catalyzed Arylation of White Phosphorus with Aryl Bromides and Chlorides<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"> <a href=\"https:\/\/doi.org\/10.1002\/adsc.70005\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.70005<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\">Abstract:<\/p>\r\n<p style=\"text-align: justify;\">A substantial improvement in the challenging photocatalytic arylation of white phosphorus (P 4) with<br>aryl chlorides and bromides is reported. Using the readily accessible deazaflavin-based photocatalyst o-Me-dFl, valuable triarylphosphines (PAr 3) and tetraarylphosphonium salts ([PAr 4]X, X = Br, Cl) are synthesized from P4 under near UV-LED (365 nm) irradiation in up to 87% combined yield with drastically reduced reaction times compared to previous protocols. 31 P nuclear magnetic resonance spectroscopic monitoring studies and density functional theory calculations provide insights into the reaction pathway. The results represent an important step toward more atom-efficient and economical photocatalytic P4 functionalization reactions.<\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Introduction of flavin anions into photoredox catalysis: Acid-base equilibria of lumichrome allows photoreductions with an anion of an elusive 10-unsubstituted isoalloxazine<\/h2>\r\n<p style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D5SC01630D\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC01630D<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Abstract:<\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><img src=\"\/images\/0!0\/uzel\/0136677\/0008~~y08qUnDOSM3VC07O1AMA.gif\" class=\"img_float_right\" alt=\" \u25f3 obr Chem.Sci. (gif) \u2192 (origin\u00e1l)\" width=\"400\" height=\"150\">Flavins have been established as effective catalysts in oxidative photoredox catalysis. Conversely, their use in reductive photocatalysis remains limited, mainly due to the relatively low stability of the transient flavin radicals (semiquinones), which are used in photoreductions. The fully reduced forms of flavins are also disadvantaged in photocatalysis because they absorb light in the UV rather than in the visible region. In this work, we present a new approach for reductive flavin photocatalysis that utilises a flavin (isoalloxazine) anion derived from the elusive 10-unsubstituted 3,7,8-trimethylisoalloxazine, an unstable tautomer of 3-methyllumichrome. We found the conditions under which this isoalloxazine anion is formed by&nbsp;<em>in situ<\/em> deprotonation\/isomerisation from the readily available 3-methyllumichrome and we subsequently used it as a photoredox catalyst in the reductive dehalogenation of activated bromoarenes and their C\u2013P coupling reaction with trimethyl phosphite to form an arylphosphonate. Steady-state and transient absorption spectroscopy, NMR and cyclic voltammetry investigations, together with quantum chemical calculations, showed that the anion of oxidised isoalloxazine has several advantages, compared to other forms of flavins used in photoreductions, such as high stability, even in the presence of oxygen, an absorption maximum in the visible region, thereby allowing the use of excitation light between 470 and 505 nm, and a relatively long-lived singlet excited-state.<\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><strong>Cover picture<\/strong>: <em>Chem. Sci.<\/em>, 2025, 16, 11681. <a href=\"https:\/\/doi.org\/10.1039\/D5SC90144H\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC90144H<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136677\/0009~~c84vSy1SKMhMLiktSgUA.png\" alt=\" \u25f3 Cover picture (png) \u2192 (origin\u00e1l)\" width=\"500\" height=\"362\"><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Divergent photoreduction of nitroaromatic compounds catalysed by dithienoquinoxaline<\/h2>\r\n<p style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2025.116033\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2025.116033<\/a><o:p><\/o:p><\/span>&nbsp;<\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"text\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><img src=\"\/images\/0!0\/uzel\/0136677\/0007~~M9QtNtIz0A02MDAytDQ1NDcyNTAwsLQw1k1PNIzPKUoHAA.jpg\" class=\"img_float_right\" alt=\" \u25f3 1-s2.0-S0021951725000983-ga1_lrg (jpg) \u2192 (origin\u00e1l)\" width=\"350\" height=\"187\">Nitroaromatic compounds can be conveniently reduced to anilines with the aid of a variety of chemical reductants. However, chemodivergent and chemoselective reduction of functionalized nitroaromatics into valuable nitroso, azo(xy), (hydr)azo and (hydroxyl)amino derivatives remains rather elusive. Electro- and photochemical strategies utilizing various catalytic systems and reaction media have been tested but most have been directed towards individual reduction products. Here, we present the photoredox-enabled chemodivergent reduction of nitroaromatics to nitroso, bis-(<em>N<\/em>,<em>O<\/em>-diacetyl)-<em>N<\/em>-arylhydroxylamine, azoxy, azo and amino derivatives. The developed protocol utilizes a novel photocatalyst, 6,9-dimethoxydithieno[2,3-<em>f<\/em>:3\u2032,2\u2032-<em>h<\/em>]quinoxaline-2,3-dicarbonitrile, and Hantzsch ester\/triethanolamine as reductants. With the single organic photocatalyst, the reaction environment, temperature, time and catalyst loading can be varied to achieve chemodivergent photoreduction of nitroaromatics bearing various functional groups and to access a library of valuable products. The application of this methodology to multigram preparations of molecules of pharmaceutical and industrial relevance highlights its practical utility.<\/span><\/p>\r\n<p style=\"text-align: center;\"><span class=\"text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids andOligopeptides via Flavin N(5)-iminium Covalent Adducts<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1002\/adsc.202401556\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.202401556<\/a><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\">Flavin co-factors and other flavin derivatives are traditionally associated with one- or two-electron redox reactions. Flavins also form covalent intermediates with a variety of substrates. While extensive attention has focused on reactions at the C(4a) position of the flavin ring, recent interest has shifted toward the dynamic potential of the N(5) atom. In our study, we demonstrate the formation of artificial flavin N(5)-iminium covalent adducts via nucleophilic attack by enolates derived from arylacyl esters at the flavin N(5) position. This interaction mimics the biosynthesis of ether phospholipids catalysed by alkyl-dihydroxyacetone phosphate synthase via an N(5)-FAD iminium adduct formation and fatty acid release. Accordingly, we developed a method for the selective removal of phenacyl and 2-naphthylacetyl protecting groups from the C-terminus of \u03b1-amino acids and di- and tripeptides using biomimetic flavin organocatalysis. Although many approaches are currently available for protection of C-terminus of peptides, their removal often requires harsh conditions, which cause racemization and the loss of optical purity, together with other side reactions. Our method is versatile, mild, orthogonal to most functional and protecting groups and maintains optical purity of \u03b1-amino acids. From general point of view, the method signifies the groundbreaking application of the non-canonical reactivity of flavins in organic synthesis.<\/p>\r\n<p style=\"text-align: justify;\"><span style=\"font-size: 12.0pt;\"><strong><span style=\"font-size: 12.0pt; line-height: 107%; font-family: source_sans_proregular; color: #464646; background: white;\">recognized by Synfacts (<\/span><span style=\"font-family: 'Segoe UI',sans-serif;\">H. Yamamoto and T. Hattori: Synfacts 2025 Vol. 21 Issue 05 Pages 543-543, <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2558-1150\" target=\"_blank\" rel=\"noopener\">DOI: 10.1055\/a-2558-1150<\/a>)<\/span><\/strong><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Chemoselective Anaerobic Dehydrogenation of Alcohols by Using Visible Light and a Positively Charged Deazaflavin Catalyst Regenerated by Acetonitrile Solvent<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1002\/cctc.202401795\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.202401795<\/a><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span>Three series of novel deazaflavinum salts differing in their substitutions at positions 5 (R&nbsp;=&nbsp;H, phenyl, or mesityl), 7, and 8 (R&nbsp;=&nbsp;OMe, Me, H, or Cl) were synthesized as potential catalysts of a novel chemoselective visible light-mediated anaerobic oxidation of primary and secondary alcohols to carbonyl compounds. This mild procedure uses acetonitrile as a solvent, which acts simultaneously as a sacrificial electron acceptor (in place of the oxygen usually used in photooxidation reactions), and therefore the reaction does not need any additives. Structure and properties-versus-catalytic activity studies identified 5-mesityl-7,8-dimethoxy-3-methyldeazaflavinium chloride (<\/span><b>3a-Cl<\/b><span>) as the most potent catalyst.&nbsp;<\/span><b>3a-Cl<\/b><span>&nbsp;was effective in non-deuterated acetonitrile (CH<\/span><sub>3<\/sub><span>CN), unlike its original 5-phenyl analogue&nbsp;<\/span><b>2a-Cl<\/b><span>, which is efficient only in deuterated solvent (CD<\/span><sub>3<\/sub><span>CN). This difference arises because the regeneration of the&nbsp;<\/span><b>2a-Cl<\/b><span>&nbsp;catalyst is slower in CH<\/span><sub>3<\/sub><span>CN than in CD<\/span><sub>3<\/sub><span>CN. Our method using the optimized&nbsp;<\/span><b>3a-Cl<\/b><span>&nbsp;photocatalyst and CH<\/span><sub>3<\/sub><span>CN as a sacrificial oxidant and solvent in one is a useful addition to synthetic organic chemistry. Anaerobic conditions prevent side oxygenation reactions and overoxidations that usually occur in air or oxygen. This property makes this method suitable for dehydrogenations of alcohols that possess additional group(s) sensitive to oxygenation.<\/span><\/p>\r\n<p><span><img src=\"\/images\/0!0\/uzel\/0136677\/0006~~y08qAgA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 obr (png) \u2192 (origin\u00e1l)\" width=\"280\" height=\"156\"><br><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span>Chemoselective anaerobic dehydrogenation of primary and secondary alcohols to carbonyl compounds that leaves intact of additional oxygenation-sensitive functional groups is possible using a new flavin catalyst, 400 nm light, and acetonitrile, which acts simultaneously as a solvent and sacrificial oxidant. No other additives needed.<\/span><span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"c-article-title\" data-test=\"article-title\" style=\"text-align: center;\">Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivative<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.1038\/s41598-024-75239-x\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41598-024-75239-x<\/a><\/span><\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><\/span><\/span><\/span>Abstract:<br><span>Incorporation of the trimethoxyphenyl group at position 7 of flavin can drastically change the photophysical properties of flavin. We show unique fast singlet&nbsp;<\/span><sup>1<\/sup><span>(\u03c0,\u03c0*) excited state deactivation pathway through nonadiabatic transition to the&nbsp;<\/span><sup>1<\/sup><span>(n,\u03c0*) excited- state, and subsequent deactivation to the ground electronic state (S<\/span><sub>0<\/sub><span>), closing the photocycle. This mechanism explains the exceptionally weak fluorescence and the short excited\u2013state lifetime for the flavin trimethoxyphenyl derivative and the lack of excited triplet T<\/span><sub>1<\/sub><span>&nbsp;state formation. Full recovery of flavin in its ground state takes place within a 15 ps time window after photoexcitation in a polar solvent such as acetonitrile. According to quantum chemical calculations, the C<\/span><sub>(2)<\/sub><span>-O distance elongates by 0.16 \u00c5 in the&nbsp;<\/span><sup>1<\/sup><span>(n,\u03c0*) state, with respect to the ground state. Intermediate\u2013state structures are predicted by theoretical ab initio calculations and their dynamics are investigated using broadband vis-NIR time-resolved transient absorption and fluorescence up-conversion techniques.<\/span><\/p>\r\n<hr>\r\n<h2 class=\"px-4 pt-6 md:px-6\" style=\"text-align: center;\">A facile three-component route to powerful 5-aryldeazaalloxazine photocatalysts<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.3762\/bjoc.20.161\" target=\"_blank\" rel=\"noopener\">DOI:10.3762\/bjoc.20.161<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span>Functionalized 5-aryldeazaalloxazines have been successfully synthesised through a one-pot, three-component reaction involving&nbsp;<\/span><i>N,N<\/i><span>-dimethylbarbituric acid, an aromatic aldehyde and aniline. By utilizing readily available reagents, this approach opens up the opportunity for the efficient formation of a variety of 5-aryldeazaalloxazines bearing electron-donating or halogen groups. This practical method is characterised by atom economy and offers a direct route to the introduction of an aryl moiety into the C(5)-position of deazaalloxazines, thereby generating novel catalysts for photoredox catalysis without the need for subsequent purification. Thus, it significantly improves existing approaches.<\/span><\/p>\r\n<p style=\"text-align: center;\"><span><img src=\"https:\/\/www.beilstein-journals.org\/bjoc\/content\/figures\/1860-5397-20-161-graphical-abstract.svg?max-width=550&amp;background=ffffff\" class=\"img-responsive margin-sm-top__small margin-md-top__small\" alt=\"Graphical Abstract\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"article_header-title\" style=\"text-align: center;\" tabindex=\"0\"><span class=\"hlFld-Title\" property=\"headline\">Ultrafast Events of Photoexcited Iron(III) Chloride for Activation of Benzylic C\u2013H Bonds<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"hlFld-Title\" property=\"headline\"><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jpclett.4c01116\" target=\"_blank\" rel=\"noopener\">DOI:10.1021\/acs.jpclett.4c01116<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"hlFld-Title\" property=\"headline\">Abstract:<br><span><img src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.jpclett.4c01116\/asset\/images\/medium\/jz4c01116_0007.gif\" class=\"img_float_right img_fancy_no\" alt=\"Figure 1\" width=\"250\">The usage of rare-earth-metal catalysts in the synthesis of organic compounds is widespread in chemical industries but is limited owing to its environmental and economic costs. However, recent studies indicate that abundant-earth metals like iron(III) chloride can photocatalyze diverse organic transformations using blue-light LEDs. Still, the underlying mechanism behind such activity is debatable and controversial, especially in the absence of ultrafast spectroscopic results. To address this urgent challenge, we performed femtosecond time-resolved electronic absorption spectroscopy experiments of iron(III) chloride in selected organic solvents relevant to its photocatalytic applications. Our results show that the long-lived species [Fe(II) \u2190 Cl<\/span><sup>\u2022<\/sup><span>]* is primarily responsible for both oxidizing the organic substrate and reducing molecular oxygen through the diffusion process, leading to the final product and regenerating the photocatalyst rather than the most widely proposed free chloride radical (Cl<\/span><sup>\u2022<\/sup><span>). Our study will guide the rational design of efficient earth-abundant photocatalysts.<\/span><br><\/span><\/p>\r\n<hr>\r\n<h2 class=\"capsule__title fixpadv--m\" style=\"text-align: center;\">Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled using DMSO as the solvent<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1039\/D4GC00087K\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D4GC00087K<\/a><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span><img src=\"https:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=D4GC00087K&amp;imageInfo.ImageIdentifier.Year=2024\" class=\"img_float_right img_fancy_no\" alt=\"Graphical abstract: Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled using DMSO as the solvent\" width=\"400\">The drawbacks commonly observed in synthetic methods for alcohol oxidation often stem from the utilization of complex, toxic, hazardous, or waste-producing oxidants. When sensitive or complex substrates bearing several functional groups are to be transformed, the selectivity of oxidation becomes another significant challenge. Herein, a chemoselective and operationally simple catalyst-free and additive-free method is presented for the aerial oxidation of 1-phenylpropargyl and 1-phenylallyl alcohols to their corresponding ketones, requiring only a solvent and visible light irradiation. The crucial role of dimethylsulfoxide (DMSO) as the solvent lies in achieving high chemoselectivity. Singlet oxygen, whose formation is photosensitized by the substrate and the product, is captured by DMSO, thereby preventing the undesired over-oxidation that occurs in other solvents. The application of DMSO to protect the substrate against singlet oxygen represents a novel approach that is potentially applicable to other aerobic photocatalytic processes.<\/span><\/p>\r\n<hr>\r\n<h2 id=\"screen-reader-main-title\" class=\"Head u-font-serif u-h2 u-margin-s-ver\" style=\"text-align: center;\"><span class=\"title-text\">Dicyanopyrazine photoredox catalysts: Correlation of efficiency with photophysics and electronic structure<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"title-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2024.115348\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2024.115348<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"title-text\">Abstract:<br><span><img src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0021951724000617-ga1.jpg\" class=\"img_float_right img_fancy_no\" width=\"300\">Catalytic performance of three structurally-related dicyanopyrazine catalysts has been investigated in three photoredox transformations including deuteration of aldehydes, cross-coupling of iodo-substituted (hetero)aromatic substrates, and \u03b1-hydrogen abstraction from amines followed by annulation to pyrroloquinoline. Significantly different catalytic activity of the photocatalysts has been explained with the aid of electrochemical, spectroscopic, and quantum-chemical methods. Electrochemical measurements pointed to reversible one-electron reduction of the photocatalysts affording the corresponding radical anion, and, therefore, dicyanopyrazines are principally well-suited for reductive quenching cycle. Triplet excited state turned out to be a major excited species employed in photoinduced electron transfer. The measured excited state reduction potentials (<\/span><em>E<\/em><sub>red<\/sub><span>* = +1.88\/+1.43&nbsp;V) classify the (5\u2013methoxy)thiophene-substituted dicyanopyrazines among the organic photocatalysts with high oxidation power, which is in contrast to&nbsp;<\/span><em>N<\/em><span>,<\/span><em>N<\/em><span>-dimethylanilino-substituted photocatalysts. Whereas 5\u2013methoxythiophene photocatalyst forms triplet excited state almost independently on the solvent polarity, transient absorption spectroscopy evidenced the triplet state of&nbsp;<\/span><em>N<\/em><span>,<\/span><em>N<\/em><span>-dimethylanilino derivative only in nonpolar media. Moreover, its subsequent reduction to the corresponding radical anion is chemically cumbersome, which contrast to facile one-electron reduction of both cyano groups of photocatalyst bearing weak 5\u2013methoxythiophene donors. The doublet excited radical anion of the latter proved to be very powerful but short-lived reductant with&nbsp;<\/span><em>E<\/em><sub>ox<\/sub><span>* = \u20132.84&nbsp;V. Its reduction power has been demonstrated in a cross-coupling reaction involving consecutive photoinduced electron transfer to preassociated iodo(hetero)arenes. Hence, bis(5-methoxythiophen-2-yl)-2,3-dicyanopyrazine can be utilized in photoredox catalysis either as powerful oxidant or reductant.<\/span><br><\/span><span class=\"title-text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" lang=\"en\" style=\"text-align: center;\">Exploring the Reactivity of Flavins with Nucleophiles Using a Theoretical and Experimental Approach<\/h2>\r\n<p style=\"text-align: center;\"><span class=\"hlFld-Title\"><a href=\"https:\/\/doi.org\/10.1002\/cplu.202300547\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cplu.202300547<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"hlFld-Title\">Abstract:<br><span>Covalent adducts of flavin cofactors with nucleophiles play an important role in non-canonical function of flavoenzymes as well as in flavin-based catalysis. Herein, the interaction of flavin derivatives including substituted flavins (isoalloxazines), 1,10-ethylene-bridged flavinium salts, and non-substituted alloxazine and deazaflavin with selected nucleophiles was investigated using an experimental and computational approach. Triphenylphosphine or trimethylphosphine, 1-nitroethan-1-ide, and methoxide were selected as representatives of neutral soft, anionic soft, and hard nucleophiles, respectively. The interactions were investigated using UV\/Vis and <\/span><sup>1<\/sup><span>H NMR spectroscopy as well as by DFT calculations. The position of nucleophilic attack estimated using the calculated Gibbs free energy values was found to correspond with the experimental data, favouring the addition of phosphine and 1-nitroethan-1-ide into position N(5) and methoxide into position C(10a) of 1,10-ethylene-bridged flavinium salts. The calculated Gibbs free energy values were found to correlate with the experimental redox potentials of the flavin derivatives tested. These findings can be utilized as valuable tools for the design of artificial flavin-based catalytic systems or investigating the mechanism of flavoenzymes.<\/span><br><\/span><\/p>\r\n<p><span class=\"hlFld-Title\"><span><img src=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/cms\/asset\/cd82f6d2-708c-4669-8efe-d0c3b0139981\/cplu202300547-toc-0001-m.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"Description unavailable\" width=\"450\"><\/span><\/span><\/p>\r\n<p style=\"text-align: center;\" class=\"article_header-title\"><span class=\"hlFld-Title\"><span>The ability of flavin derivatives to add a nucleophile can be quantified and the regioselectivity estimated by Gibbs free energy values calculated by DFT methods. The theoretical data corresponds to the results obtained by&nbsp;<\/span><sup>1<\/sup><span>H NMR and UV\/Vis spectroscopy and to experimental flavin reduction potentials.<\/span><\/span><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["15408"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. Cibulka research group","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"10.06.2026 11:19:00","platne_do":null,"iduzel":"15408","class":"infobox","autonomni":"0","pod_uzly":["15431","15431","15431","15414","15414","15414","16013","16013","16013","15412","15412","15412","15413","15413","15413"],"poduzly_count":15,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15431":{"idvazba":"18864","nad_uzel":"15408","pod_uzel":"15431","url":"","sablona":null,"nazev":"Home","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 14:39:00","platne_do":null,"iduzel":"15431","obsah":"a:4:{s:4:\"akce\";s:4:\"Home\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:17:\"\/research\/cibulka\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15414":{"idvazba":"18838","nad_uzel":"15408","pod_uzel":"15414","url":"","sablona":null,"nazev":"People","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"07.06.2026 20:57:00","platne_do":null,"iduzel":"15414","obsah":"a:4:{s:4:\"akce\";s:6:\"People\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:22:\"\/research\/cibulka\/lide\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"16013":{"idvazba":"19734","nad_uzel":"15408","pod_uzel":"16013","url":"","sablona":null,"nazev":"Research","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"07.06.2026 20:59:00","platne_do":null,"iduzel":"16013","obsah":"a:4:{s:4:\"akce\";s:8:\"Research\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:24:\"\/research\/cibulka\/Vyzkum\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15412":{"idvazba":"18836","nad_uzel":"15408","pod_uzel":"15412","url":"","sablona":null,"nazev":"Publications","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"07.06.2026 20:58:00","platne_do":null,"iduzel":"15412","obsah":"a:4:{s:4:\"akce\";s:12:\"Publications\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:27:\"\/research\/cibulka\/publikace\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15413":{"idvazba":"18837","nad_uzel":"15408","pod_uzel":"15413","url":"","sablona":null,"nazev":"Projects","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"07.06.2026 20:58:00","platne_do":null,"iduzel":"15413","obsah":"a:4:{s:4:\"akce\";s:8:\"Projects\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:24:\"\/research\/cibulka\/granty\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0}}}}},"136681":{"idvazba":"170878","nad_uzel":"136669","pod_uzel":"136681","url":"\/research\/cibulka\/vyuka","sablona":"58","nazev":"V\u00fduka","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/vyuka}","poradi":"8","skupina_www":"everyone","platne_od":"04.06.2026 11:36:00","platne_do":null,"iduzel":"136681","obsah":"a:13:{s:5:\"nazev\";s:6:\"V\u00fduka\";s:9:\"seo_title\";s:6:\"V\u00fduka\";s:8:\"seo_desc\";s:6:\"V\u00fduka\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:29:\"0002~~K87JTEktUiirLM1OBAA.jpg\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:2361:\"<p><\/p>\r\n<h3>Prof. Ing. Radek Cibulka, Ph.D.<\/h3>\r\n<ul>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110001\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie A<\/a> - p\u0159edn\u00e1\u0161ky<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110002\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie B<\/a> - p\u0159edn\u00e1\u0161ky<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=M110004\" target=\"_blank\" rel=\"noopener\">Retrosynt\u00e9za<\/a> - p\u0159edn\u00e1\u0161ky<\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<h3>Mgr. Roman Holakovsk\u00fd, Ph.D.<\/h3>\r\n<ul>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110001\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie A<\/a> - semin\u00e1\u0159e<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110002\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie B<\/a> - semin\u00e1\u0159e<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110009\" target=\"_blank\" rel=\"noopener\">Z\u00e1klady farmakochemie<\/a> - p\u0159edn\u00e1\u0161ky<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110005\" target=\"_blank\" rel=\"noopener\">Laborato\u0159e organick\u00e9 chemie I<\/a><\/li>\r\n<li><a href=\"https:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110006\" target=\"_blank\" rel=\"noopener\">Laborato\u0159e organick\u00e9 chemie II<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<h3>Ing. Eva Svobodov\u00e1, Ph.D.<\/h3>\r\n<ul>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110001\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie A<\/a> - semin\u00e1\u0159e<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110002\" target=\"_blank\" rel=\"noopener\">Organick\u00e1 chemie B<\/a> - semin\u00e1\u0159e<\/li>\r\n<li><a href=\"http:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110005\" target=\"_blank\" rel=\"noopener\">Laborato\u0159e organick\u00e9 chemie I<\/a><\/li>\r\n<li><a href=\"https:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=B110006\" target=\"_blank\" rel=\"noopener\">Laborato\u0159e organick\u00e9 chemie II<\/a><\/li>\r\n<li><a href=\"https:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=M110010\">Laborato\u0159 specializace - synt\u00e9za l\u00e9\u010div<\/a><\/li>\r\n<li><a href=\"https:\/\/student.vscht.cz\/predmety\/index.php?do=predmet&amp;kod=M110019\">Laborato\u0159 specializace - organick\u00e1 chemie<\/a><\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["15408"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. 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2026 - 2028)<br><\/span><span><\/span><\/li>\r\n<li><span>Fotoredoxn\u00ed katal\u00fdza s organick\u00fdmi anionty - perspektivn\u00ed oblast pro flavinov\u00e9 deriv\u00e1ty<br>Photoredox catalysis with organic anions - perspective area for flavin derivatives<br>(GA\u010cR 24-11386K; 2023 - 2026; Czech-Poland joint project)<\/span><\/li>\r\n<li>Spojen\u00ed fotochemie a elektrochemie v redoxn\u00ed katal\u00fdze na b\u00e1zi flavin\u016f<br>Merging photochemistry and elecktrochemistry in flavin-based redox catalysis<br>(GA\u010cR <span>23-06465S<\/span>; 2023 - 2025)<\/li>\r\n<li>C\u00edlen\u00fd n\u00e1vrh flavin\u016f pro organickou fotokatal\u00fdzu<br>Tailoring flavins for organic photocatalysis<br>(GA\u010cR 21-14200K; 2021 - 2023; <span>Czech-Poland joint project<\/span>)<\/li>\r\n<li>Nov\u00e1 strategie p\u0159ep\u00f3lov\u00e1n\u00ed s vyu\u017eit\u00edm kovalentn\u00ed organokatal\u00fdzy s flaviny<br>Novel umpolung strategy using flavin covalent organocatalysis<br>(GA\u010cR 21-14179S; 2021 - 2023)<\/li>\r\n<li>Organick\u00e1 fotoredoxn\u00ed katal\u00fdza v reduk\u010dn\u00edch transformac\u00edch: nov\u00fd prostor pro deriv\u00e1ty flavin\u016f<br>Organic photoredox catalysis in reductive transformations: new area for flavin derivatives<br>(GA\u010cR 19-09064S; 2019 - 2021)<\/li>\r\n<li>Oxidativn\u00ed fotokatalytick\u00e9 syst\u00e9my s flaviniov\u00fdmi solemi pro p\u0159\u00edm\u00e9 C-H funkcionalizace<br>Oxidative photocatalytic systems with flavinium salts for direct <span>C\u2013H functionalizations<\/span><br>(GA\u010cR 18-15175S; 2018 - 2020)<\/li>\r\n<li>Fotokatalytick\u00e1 a organokatalick\u00e1 Mitsunobuova reakce s vyu\u017eit\u00edm deriv\u00e1t\u016f flavin\u016f a viditeln\u00e9ho sv\u011btla <br>Photocatalytic and Organocatalytic Mitsunobu Reaction Mediated by Flavin derivatives and Visible Light<br>(GA\u010cR 16-09436S; 2016 - 2018)<\/li>\r\n<li>Fotoorganokatalytick\u00e1 metateze: [2+2] cykloadice alkenu a \u0161t\u011bpen\u00ed cyklobutanov\u00e9ho kruhu s vyu\u017eit\u00edm flavinu a viditeln\u00e9ho sv\u011btla<br>Towards photoorganocatalytic metathesis: [2+2] cycloaddition of alkenes and cyclobutane ring cleavage mediated by flavins and visible light<br>(GA\u010cR 14-09190S; 2014 - 2016)<\/li>\r\n<li>Nov\u00e9 deriv\u00e1ty flavin\u016f pro fotokatal\u00fdzu s vyu\u017eit\u00edm viditeln\u00e9ho sv\u011btla<br>New flanin derivatives for visible light photocatalysis<br>(M\u0160MT 7AMB14PL010; 2014 - 2015)<\/li>\r\n<li>Organokatalytick\u00e9 stereoselektivn\u00ed oxidace s vyu\u017eit\u00edm heterocyklick\u00fdch hydroperoxid\u016f<br>Organocatalytic stereoselective oxidations using heterocyclic hydroperoxides<br>(GA\u010cR P207\/12\/0447; 2012 - 2015)<\/li>\r\n<li>Chir\u00e1ln\u00ed flaviniov\u00e9 soli jako katalyz\u00e1tory enantioselektivn\u00edch sulfoxidac\u00ed a N-oxidac\u00ed<br>Chiral flavinium salts as organocatalysts for enantioselective sulfoxidations and N-oxidations<br>(GA\u010cR 203\/07\/1246; 2007 - 2011)<\/li>\r\n<li>Nov\u00e9 katalyz\u00e1tory oxida\u010dn\u00edch reakc\u00ed zalo\u017een\u00e9 na amfifiln\u00edch flavinech<br>Novel catalysts of oxidation reactions based on amphiphilic flavins<br>(M\u0160MT 1K04105; 2004 - 2007)<br><br><\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["15408"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. 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Photobiol. Sci. <\/i><b>2026<\/b>, <em>25<\/em>, 935-949.&nbsp;<a href=\"https:\/\/doi.org\/10.1007\/s43630-026-00893-1\">DOI:10.1007\/s43630-026-00893-1<\/a>.<\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Sponar R., Li\u0161ka A., Cibulka R.: Electrochemistry Facilitates the hemoselectivity of Benzylic Alcohol Oxidations Mediated by Flavin-Based Photoredox Catalysis, <i>Org. Lett. <\/i><b>2026<\/b>, <span>&nbsp;<\/span><em><span class=\"cit-volume\">28<\/span><\/em><span class=\"cit-issue\">, <em>5<\/em><\/span><span class=\"cit-pageRange\">, 1540\u20131544<\/span>.&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.5c04603\" target=\"_blank\" rel=\"noopener\">DOI:10.1021\/acs.orglett.5c04603<\/a>.<o:p><\/o:p><\/span><\/p>\r\n<h3><span class=\"modra0\">2025<\/span><\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt; line-height: 107%;\">Weisheitelov\u00e1 I., Varma N., \u0160imkov\u00e1 L., Chudoba J., Pavlovska T., Gulaczyk I., Burdzi\u0144ski G., Ludv\u00edk J., Sikorski M., Cibulka R.: Deazaalloxazines \u2013 Flavin Derivatives That Provide Reductive Photoredox Catalysis with Inert Substrates, <i>Chem. Eur. J.<\/i> <b>2025<\/b>, 31:e02897. <a href=\"https:\/\/doi.org\/10.1002\/chem.202502897\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.202502897<\/a>.<\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">\u0160imkov\u00e1 L., Svobodov\u00e1 E., Li\u0161ka A., Lu\u0161pai K., Cibulka R., Ludv\u00edk J.: Redox properties of flavin derivatives: A Comparative study, <i>Electrochim. Acta<\/i> <b>2025<\/b>, <i>543. <\/i>&nbsp;<a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2025.147520\">DOI:10.1016\/j.electacta.2025.147520<\/a><\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Tolba A. H., El-Zohry A., Khan J. I., Svobodov\u00e1 E. Chudoba J., Kl\u00edma J., Lu\u0161pai K. Pi\u017el M., \u0160turala J., Cibulka R.: Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations <i>Nat. Commun.&nbsp;<\/i><b>2025<\/b>, <i>16<\/i>, 7851. <span class=\"identifier doi\" style=\"font-size: 15px;\"><a href=\"https:\/\/doi.org\/10.1038\/s41467-025-63233-4\" target=\"_blank\" rel=\"noopener\" data-ga-category=\"full_text\" data-ga-action=\"DOI\">DOI:10.1038\/s41467-025-63233-4<\/a><\/span><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">R\u00fcckel J., Pavlovska T., Gawrona M., Cibulka R., Wolf R.: Deazaflavin-Catalyzed Arylation of White Phosphorus with Aryl Bromides and Chlorides,&nbsp;<i>Adv. Synth. Catal.<\/i> <b>2025<\/b>, 367, e70005.&nbsp; <a href=\"https:\/\/doi.org\/10.1002\/adsc.202500435\" target=\"_blank\" rel=\"noopener\"><\/a><a href=\"https:\/\/doi.org\/10.1002\/adsc.70005\">DOI:10.1002\/adsc.70005<\/a><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Pruka\u0142a D., Zubova E., Svobodov\u00e1 E., \u0160imkov\u00e1 L., Varma N., Chudoba J., Ludv\u00edk J., Burdzinski G., Gulaczyk G., Sikorski M., Cibulka R.: Introduction of flavin anions into photoredox catalysis: Acid-base equilibria of lumichrome allows photoreductions with an anion of an elusive 10-unsubstituted isoalloxazine,&nbsp;<i>Chem. Sci. <\/i><b>2025<\/b>, <em>16<\/em>, 11255-11263.&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D5SC01630D\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC01630D<\/a><br><strong>Cover picture<\/strong>: <em>Chem. Sci.<\/em>, 2025, 16, 11681. <a href=\"https:\/\/doi.org\/10.1039\/D5SC90144H\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC90144H<\/a><\/span><\/p>\r\n<p class=\"MsoNormal\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Bure\u0161ov\u00e1<\/span> Z.,<\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt;\">&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">Grygarov\u00e1<\/span> M., Prokopov\u00e1<\/span><span class=\"react-xocs-alternative-link\"> E., Klikar<\/span> M., Pytela O.<span style=\"font-size: 12.0pt; color: #1f1f1f;\">,&nbsp;<\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">V\u00e1\u0148a J.,<span style=\"color: #1f1f1f;\">&nbsp;<\/span>Fahim M. A. M.,<span style=\"color: #1f1f1f;\">&nbsp;<\/span><\/span><\/span><span class=\"given-name\"><span style=\"font-size: 12.0pt;\">Kanyashree<\/span><\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt;\">&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">J.<\/span><\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt; color: #1f1f1f;\">,&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">Zubova E.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Bart\u00e1\u010dek J.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Tydlit\u00e1t J., R\u016f\u017ei\u010dkov\u00e1 Z.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Cibulka R., Schanze K. S.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Bure\u0161 F.: Divergent photoreduction of nitroaromatic compounds catalysed by dithienoquinoxaline, <i>J. Catal. <\/i><b>2025<\/b>, <em>445<\/em>, 116033. <a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2025.116033\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2025.116033<\/a><o:p><\/o:p><\/span><\/span>&nbsp;<span style=\"font-size: 12.0pt;\"> <\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><br><\/span><span style=\"font-size: 12.0pt;\">Pavlovska T., Havl\u00edk M., Lab\u00edkov\u00e1 M., Cibulka R.: Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids and Oligopeptides via Flavin N(5)-iminium Covalent Adducts. <i>Adv. Synth. Catal.<\/i> <b>2025<\/b>, <em>367<\/em>,&nbsp; e202401556. <a href=\"https:\/\/doi.org\/10.1002\/adsc.202401556\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.202401556<\/a>&nbsp;<br><strong><span style=\"font-size: 12.0pt; line-height: 107%; font-family: source_sans_proregular; color: #464646; background: white;\">recognized by Synfacts (<\/span><span style=\"font-family: 'Segoe UI',sans-serif;\">H. Yamamoto and T. Hattori: Synfacts 2025 Vol. 21 Issue 05 Pages 543-543, <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2558-1150\" target=\"_blank\" rel=\"noopener\">DOI: 10.1055\/a-2558-1150<\/a>)<\/span><\/strong><br><\/span><o:p><\/o:p><span style=\"font-size: 12.0pt;\"><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-family: 'Segoe UI',sans-serif;\">Obert\u00edk R., Ludv\u00edkov\u00e1 L., Chudoba J., Cibulka R.: Chemoselective Anaerobic Dehydrogenation of Alkohols By Using Visible Light and Positively Charged Deazajlavin Catalyst Regenerated by Acetonitrile Solvent. <em>ChemCatChem<\/em> <strong>2025<\/strong>, <em>17<\/em>, e202401795. <a href=\"https:\/\/doi.org\/10.1002\/cctc.202401795\">DOI:10.1002\/cctc.202401795<\/a><\/span><\/span><\/p>\r\n<h3><span class=\"modra0\">2024<\/span><\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-family: 'Segoe UI',sans-serif;\">Nizi\u0144ski S., Varma N., Sikorski M., Tobrman T., Svobodov\u00e1 E., Cibulka R., Rode M.F., Burdzinski G.: Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivate. <em>Sci Rep<\/em> <strong>2024<\/strong>, <em>14<\/em>, 24375. <span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.1038\/s41598-024-75239-x\">DOI:10.1038\/s41598-024-75239-x<\/a><\/span><\/span><\/span><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Weisheitelov\u00e1 I., Cibulka R., Sikorski M., Pavlovska T.: A facile three-component route to powerful 5-aryldeazaalloxazine photocatalysts. <i>Beilstein J. Org. Chem.<\/i> <b>2024<\/b>, <i>20<\/i>, 1831\u20131838.&nbsp; <span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.3762\/bjoc.20.161\">DOI:10.3762\/bjoc.20.161<\/a><\/span><\/span><o:p><\/o:p><span style=\"font-size: 12.0pt;\"><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-family: 'Segoe UI',sans-serif;\">Venkatraman R.K., Hassan Tolba A., Solling T., Cibulka R., El-Zohry A.: Ultrafast Events of Photoexcited Iron(III)chloride for Activation of Benzylic C<span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">\u2014<\/span>H Bonds. <em>J. Phys. Chem. Lett.<\/em> <strong>2024<\/strong>, <em>15<\/em>, 6202-6208. <span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.1021\/acs.jpclett.4c01116\">DOI:10.1021\/acs.jpclett.4c01116<\/a><\/span><\/span><\/span><span style=\"font-size: 12.0pt;\"><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Weisheitelov\u00e1 I., Varma N., Chudoba J., Burdzi\u0144ski G., Sikorski M., Cibulka R.: Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled by DMSO solvent. Green Chemistry,&nbsp;<strong>2024<\/strong>, <em>26<\/em>, 4880-4887. <a href=\"https:\/\/doi.org\/10.1039\/D4GC00087K\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D4GC00087K<\/a><\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Bure\u0161ov\u00e1 Z., Gobeze H. B., Grygarov\u00e1 M., Pytela O., Klikar M., Obert\u00edk R., Cibulka R., Islam T., Schanze K. S., Bure\u0161 F.:&nbsp;<\/span><span lang=\"EN-US\" style=\"font-size: 12.0pt; mso-ansi-language: EN-US;\">Dicyanopyrazine Photoredox Catalysts: Correlation of Efficiency with Photophysics and Electronic Structure. <i>Journal of Catalysis<\/i> &nbsp;<b>2024<\/b>, <i>430<\/i>, <\/span><span style=\"font-size: 12.0pt;\">115348.&nbsp; <a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2024.115348\" target=\"_blank\" title=\"Persistent link using digital object identifier\" rel=\"noopener\">DOI:10.1016\/j.jcat.2024.115348<\/a><\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Zubov\u00e1 E., Pokluda A., Dvo\u0159\u00e1kov\u00e1 H., Krupi\u010dka M., Cibulka R.: Exploring the Reactivity of Flavins with Nucleophiles Using a Theoretical and Experimental Approach. <em>ChemPlusChem<\/em> <strong>2024<\/strong>, e202300547. <span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.1002\/cplu.202300547\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cplu.202300547<\/a><\/span><\/span><\/p>\r\n<h3><\/h3>\r\n<h3><span class=\"modra0\">2023<\/span><\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Pavlovska T., Weisheitelov\u00e1 I., Pramthaisong C., Sikorski M., Jahn U., Cibulka R.: Primary and Secondary Amines by Flavin\u2010Photocatalyzed Consecutive Desulfonylation and Dealkylation of Sulfonamides. <i>Adv. Synth. Catal.<\/i><span>&nbsp;<\/span><strong><span class=\"pubYear\">2023<\/span><\/strong><span>,&nbsp;<\/span><em><span class=\"vol\">365<\/span><\/em><span>,&nbsp;<\/span><span class=\"pageFirst\">4662<\/span>. <a href=\"http:\/\/dx.doi.org\/DOI:10.1002\/adsc.202300843\">DOI:10.1002\/adsc.202300843<\/a>.<\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Golczak A., Pruka\u0142a D., Gierszewski M., Cherkas V., Kwiatek D., Kubiak A., Varma N., Pedzi\u0144ski T., Murphree S., Cibulka R., Mr\u00f3wczi\u0144ska L., Kolanovski J. L., Sikorski M.: Tetramethylalloxazines as efficient singlet oxygen photosensitizers and potential redox\u2011sensitive agents.&nbsp;<i>Scientific Reports <\/i><b>2023<\/b>,<i> 13<\/i>, 13426. <a href=\"http:\/\/dx.doi.org\/DOI:10.1038\/s41598-023-40536-4\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41598-023-40536-4<\/a>.&nbsp;<\/span><o:p><\/o:p><\/p>\r\n<p>Insi\u0144ska-Rak M., Golczak A., Gierszewski M., Anwar Z., Cherkas V., Kwiatek D., Sikorska E., Khmelinskii I., Burdzi\u0144ski G., Cibulka R., Mr\u00f3wczy\u0144skag L., Kolanowskic J. L. and Sikorski M.: 5-Deazaalloxazine as photosensitizer of singlet oxygen and potential redox-sensitive agent.&nbsp;<em>Photochem. Photobiol. Sci<\/em>. <strong>2023<\/strong>. <a href=\"http:\/\/dx.doi.org\/DOI:10.1007\/s43630-023-00401-9\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1007\/s43630-023-00401-9<\/a> &nbsp;<\/p>\r\n<p>Pokluda A., Zubova E., Chudoba J., Krupi\u010dka M., Cibulka R.: Catalytic Artificial Nitroalkane Oxidase \u2013 a Way Towards Organocatalytic Umpolung. <em>Org. Biomol. Chem. <\/em><strong>2023<\/strong><em>, 21, 2768 - 2774<\/em>. &nbsp;<a href=\"http:\/\/dx.doi.org\/DOI:10.1039\/D3OB00101F\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1039\/d3ob00101f<\/a>.<\/p>\r\n<h3><span class=\"modra0\">2022<\/span><\/h3>\r\n<p>\u010cubi\u0148\u00e1k M., Varma N., Oeser P., Pokluda A., Pavlovska T., Cibulka R., Sikorski M., Tobrman T. : Tuning the Photophysical Properties of Flavins by Attaching an Aryl Moiety via Direct C\u2013C Bond Coupling. <em>J. Org. Chem.<\/em>&nbsp;<strong>2022<\/strong>. <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.2c02168\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acs.joc.2c02168<\/a><\/p>\r\n<p>Obert\u00edk R., Chudoba J., \u0160turala J., Tar\u00e1bek J., Ludv\u00edkov\u00e1 L., Slanina T., K\u00f6nig B., Cibulka R.: <em>Chem. Eur. J.<\/em> <strong>2022<\/strong>, accepted as <strong>VIP<\/strong><em>. <\/em><a href=\"https:\/\/doi.org\/10.1002\/chem.202202487\" rel=\"follow\">DOI:10.1002\/chem.202202487<\/a>.<\/p>\r\n<p>Pavlovska T., Kr\u00e1l Lesn\u00fd D., Svobodov\u00e1 E., Hoskovcov\u00e1 I., Archipowa N., Kutta R. J., Cibulka R. Tuning Deazaflavins Towards Highly Potent Reducing Photocatalysts Guided by Mechanistic Understanding - Enhancement of the Key Step by the Internal Heavy Atom Effect. <em>Chem. Eur. J.<\/em> <strong>2022<\/strong>, <em>28<\/em>, e20220076. <strong>Hot Paper<\/strong>.&nbsp; <a href=\"http:\/\/doi.org\/10.1002\/chem.202200768\" rel=\"follow\">DOI:10.1002\/chem.202200768<\/a>.<\/p>\r\n<p>Golczak A., Insi\u0144ska-Rak M., Davoudpour A., Saeed D. H., M\u00e9nov\u00e1 P., Mojr V., Cibulka R., Khmelinskii V., Mr\u00f3wczy\u0144ska L., Sikorski M. Photophysical properties of alloxazine derivatives with extended aromaticity \u2013 potential redox sensitive fluorescent probe. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, volume 272, <span>120985, <\/span><strong>2022<\/strong>. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.saa.2022.120985\" rel=\"follow\">DOI: 10.1016\/j.saa.2022.120985<\/a>.<\/p>\r\n<h3><span class=\"modra0\">2021<\/span><\/h3>\r\n<p>Tolba A. H., Krupi\u010dka M., Chudoba J., Cibulka R.: Amide bond formation via aerobic photooxidative coupling of alde-hydes with amines catalyzed by a riboflavin derivative <span class=\"cit-title\"><i>Org. Lett.<\/i><\/span><span>&nbsp;<\/span><span class=\"cit-year-info\"><span>2021<\/span><\/span><span class=\"cit-volume\">, 23<\/span><span class=\"cit-issue\">, 17<\/span><span class=\"cit-pageRange\">, 6825\u20136830. <\/span><a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.1c02391\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acs.orglett.1c02391<\/a>.<\/p>\r\n<p>Radek Cibulka (a prof. M. Fraaije z&nbsp;Univerzity v&nbsp;Groningenu) editory knihy \u201eFlavin-Based catalysis\u201c v&nbsp;nakladatelstv\u00ed Wiley-VCH. Z\u00e1rove\u0148 \u010dlenov\u00e9 na\u0161\u00ed skupiny p\u0159ipravili t\u0159i z&nbsp;dvan\u00e1cti kapitol v&nbsp;t\u00e9to knize:<br>Pavlovska, T.; Cibulka, R., Structure and Properties of Flavins. pp 1-27.<br>Cibulka, R.; Fraaije, M. W., Modes of Flavin-Based Catalysis. pp 97-124.<br>Svobodov\u00e1, E.; Cibulka, R., New Applications of Flavin Photocatalysis. pp 265-291.<br><a href=\"https:\/\/www.wiley-vch.de\/en\/areas-interest\/natural-sciences\/chemistry-11ch\/catalysis-11ch4\/flavin-based-catalysis-978-3-527-34834-3\" target=\"_blank\" rel=\"follow noopener\">Wiley-VCH - Flavin-Based Catalysis<\/a><\/p>\r\n<p>Jakubec M., Nov\u00e1k D., Zatloukalov\u00e1 M., S\u00fdkora J., C\u00edsa\u0159ov\u00e1 I., Cibulka R., Favereau L., Crassous J., Bilewicz R., Hrb\u00e1\u010d J., Storch J., \u017d\u00e1dn\u00fd J., Vacek J.: Flavin-Helicene Amphiphilic Hybrids: Synthesis, Characterization, and Preparation of Surface-Supported Films <span>&nbsp;<\/span><i>ChemPlusChem<\/i><span>&nbsp;<\/span><b>2021<\/b><span>,&nbsp;<\/span><i>86<\/i><span>, 982-990<\/span>. <a href=\"http:\/\/dx.doi.org\/10.1002\/cplu.202100092\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cplu.202100092<\/a>.<\/p>\r\n<p style=\"text-align: left;\">Pokluda A., Anwar Z., Boguschov\u00e1 V., Anusiewicz I., Skurski P., Sikorski M., Cibulka R.: Robust photocatalytic method using ethylene-bridged flavinium salts for the aerobic oxidation of unactivated benzylic substrates <em>Adv. Synth. Catal.<\/em> <strong>2021<\/strong> <em>363<\/em>, 4371-4379. <strong>VIP<\/strong>. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.202100024\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1002\/adsc.202100024<\/a>.<br><span class=\"oranzova0\"><strong><\/strong><\/span><\/p>\r\n<p style=\"text-align: center;\"><span class=\"oranzova0\"><strong>&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/adsc.202100748\" target=\"_blank\" rel=\"follow noopener\">\u201eTituln\u00ed obr\u00e1zek\u201c<\/a><\/strong><\/span><\/p>\r\n<p style=\"text-align: left;\">Hartman T., Reisnerov\u00e1 M., Chudoba J., Svobodov\u00e1 E., Archipowa N., Kutta R. J., Cibulka R.: Photocatalytic Oxidative [2+2] Cycloelimination Reactions with Flavinium Salts: Mechanistic Study and Influence of the Catalyst Structure <em>ChemPlusChem<\/em> <strong>2021<\/strong>, <em>86<\/em>, 373\u2013386. <a href=\"http:\/\/dx.doi.org\/10.1002\/cplu.202000767\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1002\/cplu.202000767.<br><\/a><\/p>\r\n<p style=\"text-align: center;\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><strong><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\">&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\">\u201eTituln\u00ed obr\u00e1zek\u201c<\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><\/strong><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/p>\r\n<p style=\"text-align: left;\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"cerna0\">Eigner, V\u00e1clav and Holakovsk\u00fd, Roman. \"The crystal structure of 2-(4-((carbamimidoylthio)methyl)benzyl)isothiouronium hexafluorophosphate monohydrate, C<sub>10<\/sub>H<sub>17<\/sub>F<sub>6<\/sub>N<sub>4<\/sub>OPS<sub>2<\/sub>\"&nbsp;<i>Zeitschrift f\u00fcr Kristallographie - New Crystal Structures<\/i>, vol. , no. , 2021. <a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0417\" rel=\"follow\">doi.org\/10.1515\/ncrs-2021-0417<\/a><\/span><a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0417\"><\/a><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"oranzova0\"><span class=\"cerna0\"><span>Eigner, V\u00e1clav and Holakovsk\u00fd, Roman. \"Crystal structure of 2-(3-((carbamimidoylthio)methyl)benzyl)isothiouronium hexafluorophosphate monohydrate, C<\/span><sub>10<\/sub><span>H<\/span><sub>17<\/sub><span>F<\/span><sub>6<\/sub><span>N<\/span><sub>4<\/sub><span>OPS<\/span><sub>2<\/sub><span>&nbsp;\"&nbsp;<\/span><i>Zeitschrift f\u00fcr Kristallographie - New Crystal Structures<\/i><span>, vol. , no. , 2021. &nbsp;<\/span><a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0418\" rel=\"follow\">doi.org\/10.1515\/ncrs-2021-0418<\/a><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/span><\/p>\r\n<h3><span class=\"modra0\">2020<\/span><\/h3>\r\n<p>Graml A., Nevesel\u00fd T., Kutta R.-J., Cibulka R., K\u00f6nig B.: Deazaflavin reductive photocatalysis involves excited semiquinone radicals <em>Nature Comm.<\/em> <strong>2020<\/strong>, <em>11<\/em>, 3174. &nbsp;DOI: 10.1038\/s41467-020-16909-y. <a href=\"https:\/\/rdcu.be\/b47PV\">https:\/\/rdcu.be\/b47PV<\/a><\/p>\r\n<p>Cibulka R.: Strong chemical reducing agents produced by light <em>Nature<\/em> <strong>580<\/strong>, 31-32 (2020). DOI: 10.1038\/d41586-020-00872-1. <a href=\"https:\/\/www.nature.com\/articles\/d41586-020-00872-1\">https:\/\/www.nature.com\/articles\/d41586-020-00872-1<\/a><\/p>\r\n<p class=\"MsoNormal\"><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">Tolba A. H., V\u00e1vra F., Chudoba J., Cibulka R: Tuning flavin-based photocatalytic systems for application in the mild chemoselective aerobic oxidation of benzylic substrates <\/span><\/span><em><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">Eur. J. Org. Chem.<\/span><\/em><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\"> <\/span><\/span><strong><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">2020<\/span><\/strong><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">, 1579\u20131585. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201901628\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; border: currentColor;\" rel=\"noopener\"><span style=\"color: #464646;\">DOI:10.1002\/ejoc.201901628<\/span><\/a>.&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/toc\/10990690\/2020\/2020\/10\" target=\"_blank\" title=\"Special issue Photochemical synthesis\" rel=\"noopener\"><strong><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: black; mso-color-alt: windowtext; text-decoration: none; text-underline: none;\">Special issue Photochemical synthesis<\/span><\/strong>.<\/a><\/span><o:p><\/o:p><\/span><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span style=\"background-color: #ffffff; border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; display: inline; float: none; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><\/span><\/span><\/p>\r\n<p class=\"MsoNormal\"><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">Schlosser J., Cibulka R., Gro\u00df P., Ihmels H., Mohrschladt C. J.: Visible-light induced di-\u03c0-methane rearrangement of dibenzobarrelene derivatives <\/span><\/span><em><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">ChemPhotoChem<\/span><\/em><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\"> <\/span><\/span><strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; border: currentColor;\"><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #333333; background: white;\">2020<\/span><\/strong><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">, <\/span><\/span><em><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">4<\/span><\/em><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\">, 132. <a href=\"http:\/\/dx.doi.org\/10.1002\/cptc.201900221\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; border: currentColor;\" rel=\"noopener\"><span style=\"color: #464646;\">DOI:10.1002\/cptc.201900221<\/span><\/a>.<\/span><\/span><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin;\"><o:p><\/o:p><\/span><\/p>\r\n<p><\/p>\r\n<h3><span class=\"modra0\">2019<\/span><\/h3>\r\n<p class=\"MsoNormal\"><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646;\">Zelenka J., Cibulka R., Roithov\u00e1, J.:&nbsp;<\/span><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; orphans: 2; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; border: currentColor; word-spacing: 0px;\">Flavinium catalyzed photooxidation: Detection and characterization of elusive peroxyflavinium intermediates. <\/span><\/span><em><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646;\">Angew. Chem. Int. Ed.<\/span><\/em><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646;\"> <\/span><\/span><strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; border: currentColor;\"><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #333333;\">2019<\/span><\/strong><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646;\">, <em>58<\/em>, 15412-15420.<span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; orphans: 2; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; border: currentColor; word-spacing: 0px;\"> <a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201906293\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; font-style: inherit; font-weight: inherit; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; border: currentColor;\" rel=\"noopener\"><span style=\"color: #464646;\">DOI:10.1002\/anie.201906293.<\/span><\/a><\/span> <\/span><\/span><strong><span style=\"font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-theme-font: minor-latin; color: #464646;\">VIP&nbsp;<\/span><\/strong><span class=\"cerna0\"><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: #464646; background: white;\"><o:p><\/o:p><\/span><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\">M\u00e4rz M., Babor M., Cibulka R.: Flavin Catalysis Employing an N(5)-Adduct: An Application in the Aerobic Organocatalytic Mitsunobu Reaction&nbsp;<em>Eur. J. Org. Chem.<\/em> <strong>2019<\/strong>, <em>20<\/em>, 3264-3268. <a href=\"https:\/\/doi.org\/10.1002\/ejoc.201900397\" rel=\"follow\">DOI:10.1002\/ejoc.201900397<\/a>.<\/span><\/p>\r\n<p style=\"margin: 0px;\"><span style=\"margin: 0px; font-size: 12pt;\"><span style=\"color: #000000; font-family: Calibri;\">Pokluda A., Kohout M., Chudoba J., Krupi\u010dka M., Cibulka R.: Nitrosobenzene \u2013 Reagent for the Mitsunobu Esterification Reaction <em>ACS Omega<\/em> <strong>2019<\/strong>, <em>4<\/em>, 5012-5018. <a href=\"https:\/\/doi.org\/10.1021\/acsomega.8b03551\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acsomega.8b03551.<\/a><\/span><\/span><\/p>\r\n<p><\/p>\r\n<p><span style=\"font-size: 12pt; font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\">Valenta L., Kova\u0159\u00ed\u010dek P., Vale\u0161 V., Bastl Z., Drogowska K. A., Verhagen T. A., Cibulka R., Kalb\u00e1\u010d M.: Spatially resolved covalent functionalization patterns on graphene <em>Angew. Chem. Int. Ed.<\/em> <strong>2019<\/strong>, <em>58<\/em>, 1324-1328. <a href=\"https:\/\/doi.org\/10.1002\/anie.201810119\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/anie.201810119<\/a>.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/anie.201810119\">https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/anie.201810119<\/a><\/span><\/p>\r\n<p><span style=\"font-size: 12pt; font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\">Zelenka J., Svobodov\u00e1 E., Tar\u00e1bek J., Hoskovcov\u00e1 I., Boguschov\u00e1 V., Bailly S., Sikorski M., Roithov\u00e1 J., Cibulka R.: Combining flavin photocatalysis and organocatalysis: metal-free aerobic oxidation of unactivated benzylic substrates <em>Org. Lett.<\/em> <strong>2019<\/strong>, <em>21<\/em>, 114-119. <a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b03547\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acs.orglett.8b03547.&nbsp;<\/a> <span class=\"cervena0\"><span class=\"cervena0\">Highly cited paper <\/span>(WOS).<\/span><\/span><\/p>\r\n<h3><span class=\"modra0\">2018<\/span><\/h3>\r\n<p>M\u00e4rz M., Kohout M., Nevesel\u00fd T., Chudoba J., Prukala D., Nizi\u0144ski S., Sikorski M., Burdzi\u0144ski G., Cibulka R.: Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control <em>Org. Biomol. Chem. <\/em><strong>2018<\/strong>, <em>16<\/em>, 6809-6817. <a href=\"https:\/\/doi.org\/10.1039\/C8OB01822G\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1039\/C8OB01822G<\/a>.<\/p>\r\n<p>Holakovsk\u00fd R., Cibulka R., Kone\u010dkov\u00e1 E., M\u00e4rz M.: Zp\u016fsob stanoven\u00ed enantiomern\u00ed \u010distoty chir\u00e1ln\u00edch sulfoxid\u016f pomoc\u00ed 1H NMR anal\u00fdzy, PV 2016-92, \u010d. 307419. Pozn. <strong>2018<\/strong><\/p>\r\n<p>K\u00f6nig B., K\u00fcmmel S., Svobodov\u00e1 E.&nbsp; and Cibulka R.: Flavin photocatalysis, <em>Physical Sciences Reviews<\/em>, 3 (8), 20170168, ISSN (Online) 2365-659X. <a href=\"https:\/\/doi.org\/10.1515\/psr-2017-0168\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1515\/psr-2017-0168.<\/a><\/p>\r\n<p>Slav\u00ed\u010dek P., Cibulka R.: A chemici nebudou m\u00edt co \u017er\u00e1t\u2026 (Strojov\u00e9 u\u010den\u00ed v&nbsp;chemii) <em>Vesm\u00edr<\/em> 97, <strong>2018 <\/strong>(5), 300-301.<br><a href=\"https:\/\/vesmir.cz\/cz\/casopis\/archiv-casopisu\/2018\/cislo-5\/a-chemici-nebudou-mit-co-zrat.html\"><span class=\"zelena0\">https:\/\/vesmir.cz\/cz\/casopis\/archiv-casopisu\/2018\/cislo-5\/a-chemici-nebudou-mit-co-zrat.html<\/span><\/a><\/p>\r\n<p class=\"t m0 xed h9 y277 ff1 fs6 fc0 sc0 ls1 ws0\"><span class=\"ff3\"><span class=\"current-selection\"><span style=\"font-size: 12.0pt;\">Muchov\u00e1 E., Bezek M., Suchan J., Cibulka R., Slav\u00ed\u010dek P.: <\/span><span style=\"font-size: 12.0pt;\">Molecular Dynamics and Metadynamics Simulations of [2+2] Photocycloaddition <em>Int. J. Quantum Chem. <\/em><strong>2018<\/strong>, <em>118<\/em>, e25534. <\/span><span style=\"font-size: 12pt;\"><a href=\"http:\/\/dx.doi.org\/10.1002\/qua.25534\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/qua.25534<\/a><\/span><\/span><\/span><\/p>\r\n<p class=\"t m0 xed h9 y277 ff1 fs6 fc0 sc0 ls1 ws0\"><span class=\"ff3\"><span class=\"current-selection\">Cu<\/span><span class=\"ff4\"><span class=\"current-selection\">\u0159<\/span><span class=\"current-selection\">\u00ednov<\/span><span class=\"current-selection\">\u00e1<\/span> <span class=\"current-selection\">P.,<\/span> <span class=\"current-selection\">Dr<\/span><span class=\"current-selection\">a<\/span><span class=\"ff4 current-selection\">\u010d<\/span><span class=\"current-selection\">\u00edn<\/span><span class=\"current-selection\">sk\u00fd <\/span><\/span><\/span><span class=\"current-selection\">M.,<\/span> <span class=\"current-selection\">Jakubec<\/span> <span class=\"current-selection\">M, Tlust\u00fd M., Jank\u016f K., Iz\u00e1k P., Holakovsk\u00fd R.:<\/span> <span class=\"current-selection\">Enantioselective<\/span> <span class=\"current-selection\">complexation <\/span><span class=\"current-selection\">of<\/span> <span class=\"current-selection\">1<\/span><span class=\"ff5 current-selection\">\u2010<\/span><span class=\"current-selection\">phenylethanol<\/span> <span class=\"current-selection\">with<\/span> <span class=\"current-selection\">chiral<\/span> <span class=\"current-selection\">comp<\/span><span class=\"current-selection\">ounds<\/span> <span class=\"current-selection\">bearing <\/span><span class=\"current-selection\">urea<\/span> <span class=\"current-selection\">moiety.<\/span> <em><span class=\"ff6\"><span class=\"current-selection\">Chirality<\/span><\/span> <\/em><span class=\"current-selection\"><strong>2018<\/strong>, <em>30, <\/em>79<\/span><span class=\"current-selection\">8<\/span><span class=\"ff5 current-selection\">\u2013<\/span><span class=\"current-selection\">806.&nbsp;<a href=\"http:\/\/doi.org\/10.1002\/chir.22855\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/chir.22855<\/a>.<\/span><\/p>\r\n<p>Mojr V., Pitrov\u00e1 G., Strakov\u00e1 K., Prukala D., Brazevic S., Svobodov\u00e1 E., Hoskovcov\u00e1 I., Burdzi\u0144ski G., Slanina T., Sikorski M., Cibulka R.: Flavin Photocatalysts for&nbsp; visible Light [2+2] Cycloadditions: Structure, Reactivity and Reaction Mechanism <em>ChemCatChem<\/em> <strong>2018<\/strong>, <em>10<\/em>, 849-858. <a href=\"http:\/\/doi.org\/10.1002\/cctc.201701490\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/cctc.201701490<\/a>.<\/p>\r\n<p>Kurfi\u0159t M., \u0160pa\u010dkov\u00e1 J., Svobodov\u00e1 E., Cibulka R.: Flavin derivatives immobilized on mesoporous silica: a versatile tool in visible-light photooxidation reactions <em>Monatshefte<\/em> <em>Chem. <\/em><strong>201<\/strong><strong>8<\/strong>, <em>149<\/em>, 863-869. <a href=\"http:\/\/doi.org\/10.1007\/s00706-017-2127-1\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1007\/s00706-017-2127-1<\/a>.<\/p>\r\n<p><\/p>\r\n<h3><span class=\"modra0\">2017<\/span><\/h3>\r\n<div class=\"clearfix\">\r\n<div class=\"grid__row\">\r\n<p class=\"x_MsoNormal\"><span style=\"font-size: 12.0pt;\">\u017durek J., Svobodov\u00e1 E., \u0160turala J., Dvo\u0159\u00e1kov\u00e1 H., Svoboda J., Cibulka R.: Chiral ethylene-bridged flavinium salts: The stereoselectivity of flavin-10a-hydroperoxide formation and the effect of substitution on the photochemical properties <em>Tetrahedron Asymmetry<\/em> <strong>2017<\/strong>, <em>28<\/em>, 1780-1791, <a href=\"http:\/\/doi.org\/10.1016\/j.tetasy.2017.10.029\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1016\/j.tetasy.2017.10.029<\/a><\/span><\/p>\r\n<p>Sofer, Z., Luxa, J., Bou\u0161a, D., Sedmidubsk\u00fd, D., Lazar, P., Hartman, T., Hardtdegen, H. and Pumera, M. , The Covalent Functionalization of Layered Black Phosphorus by Nucleophilic Reagents. <em>Angew. Chem. Int. Ed<\/em>. <strong>2017<\/strong><span class=\"ffc fs9\"><span class=\"ls48\"><span class=\"ls0\"><span class=\"ffb\"><span class=\"ffd\"><span class=\"current-selection\">,<\/span> <\/span><\/span><\/span><\/span><\/span><span class=\"ffc fs9\"><span class=\"ls48\"><span class=\"ls0\"><em><span class=\"current-selection\">56<\/span><\/em><span class=\"ffd ls48\"><span class=\"current-selection\">, 9<\/span><span class=\"current-selection\">891<\/span><span class=\"current-selection\">\u20139896<\/span><\/span><\/span><\/span><\/span>. <a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201705722\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/anie.201705722<\/a><\/p>\r\n<\/div>\r\n<\/div>\r\n<p><em><span style=\"font-style: normal;\">M\u00e4rz M., Kohout M., Chudoba J., Cibulka R.: <\/span><\/em>Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light <em>Org. Biomol. Chem.<\/em> <strong><span style=\"font-size: 12.0pt;\">2017<\/span><\/strong><em><span style=\"font-size: 12.0pt;\">, 15<\/span><\/em><span style=\"font-size: 12.0pt;\">, 1970-1975.&nbsp;<\/span> <a href=\"http:\/\/dx.doi.org\/ 10.1039\/C6OB02770A\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C6OB02770A<\/a>,&nbsp;highlighted in <span class=\"oranzova0\"><a href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2018\/12March.shtm\"><span class=\"zelena0\">http:\/\/www.organic-chemistry.org\/Highlights\/2018\/12March.shtm<\/span><\/a><\/span><a href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2018\/12March.shtm\"><\/a><\/p>\r\n<p>Kolderov\u00e1, N.; Nevesel\u00fd, T.; \u0160turala, J.; <span class=\"cerna0\">Kucha\u0159<\/span>, M.; Holakovsk\u00fd, R.; Kohout, M.: Enantioseparation of Chiral Sulfoxides on Amylose-Based Columns: Comparison of Normal Phase Liquid Chromatography and Supercritical Fluid Chromatography.&nbsp;<em>Chromatographia<\/em>&nbsp;<strong>2017<\/strong>, <em>80<\/em>, 547-557. <a href=\"http:\/\/dx.doi.org\/ 10.1007\/s10337-016-3234-6\" target=\"_blank\" rel=\"noopener\">DOI: 10.1007\/s10337-016-3234-6<\/a><\/p>\r\n<p>\u0160pa\u010dkov\u00e1 J., Svobodov\u00e1 E., Hartman T., Stibor I., Kopeck\u00e1 J., Cibulkov\u00e1 J., Chudoba J., Cibulka R.: Visible Light [2+2] Photocycloaddition Mediated by Flavin Derivative Immobilized on Mesoporous Silica, <em>ChemCatChem<\/em> <strong>2017<\/strong>, <span style=\"font-size: 12.0pt;\"><span class=\"ff5\"><em> 9<\/em>, 1177-1181<\/span><\/span>. <a href=\"http:\/\/dx.doi.org\/10.1002\/cctc.201601654\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.201601654<\/a><\/p>\r\n<p>Jir\u00e1sek M., Strakov\u00e1 K., Nevesel\u00fd T., Svobodov\u00e1 E., Rottnerov\u00e1 Z., Cibulka R.: Flavin-Mediated Visible Light <span lang=\"EN-US\">[2+2] Photocycloadditon of Nitrogen and Sulfur-Containing Dienes, <em>Eur. 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Chem.<\/em>, <strong>2012<\/strong>, 7066-7074. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201201188\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201201188<\/a><\/p>\r\n<p>Cibulka R., Jurok R.: ORGANOKATALYTICK\u00c9 ENANTIOSELEKTIVN\u00cd OXIDACE SULFID\u016e NA SULFOXIDY, <em>Chemick\u00e9 listy<\/em>, <strong>2012<\/strong>, <em>106<\/em>, 896-902. <a href=\"http:\/\/www.chemicke-listy.cz\/docs\/full\/2012_10_896-902.pdf\">http:\/\/www.chemicke-listy.cz\/docs\/full\/2012_10_896-902.pdf<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Cibulka R.: INSIGHT INTO THE CATALYTIC ACTIVITY OF ALLOXAZINIUM AND ISOALLOXAZINIUM SALTS IN THE OXIDATIONS OF SULFIDES AND AMINES WITH HYDROGEN PEROXIDE, <em>J. Mol. Catal. A: Chemical<\/em>, <strong>2012<\/strong>, <em>363-364<\/em>, 362-370. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molcata.2012.07.012\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.molcata.2012.07.012<\/a><\/p>\r\n<p>Da\u010fov\u00e1 J., Svobodov\u00e1 E., Sikorski M., K\u00f6nig B., Cibulka R.: Photooxidation of sulfides to sulfoxides mediated by tetra-O-acetylriboflavin and visible light. <em>ChemCatChem<\/em>, <strong>2012<\/strong>, <em>4<\/em>, 620-623. <a href=\"http:\/\/dx.doi.org\/10.1002\/cctc.201100372\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.201100372<\/a><\/p>\r\n<p>Tiskov\u00e1 zpr\u00e1va:<a href=\"http:\/\/www.chemistryviews.org\/details\/ezine\/2048673\/Blue_Light_District_Sulfide_Photooxidation.html\">\"Blue Light District: Sulfide Photooxidation\" (ChemistryViews.org)<\/a><\/p>\r\n<h3><span class=\"modra0\">2011<\/span><\/h3>\r\n<p>Mojr V., Budesinsky M., Cibulka R., Kraus T.: Alloxazine-cyclodextrin conjugates for organocatalytic enantioselective sulfoxidations. <em>Org. Biomol. Chem.<\/em>, <strong>2011<\/strong>, <em>9<\/em>, 7257-7580. <a href=\"http:\/\/dx.doi.org\/10.1039\/C1OB05934C\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C1OB05934C<\/a> + <a href=\"\/files\/uzel\/0007830\/cover3_pdf.pdf\" target=\"_blank\" rel=\"noopener\">Cover picture<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Eigner V., \u010cejka J., Dvo\u0159\u00e1kov\u00e1 H., \u0160anda M., Cibulka R.: Synthesis and structural studies of flavin and alloxazine adducts with O-nucleophiles. <em>J. Mol. Struct. <\/em><strong>2011<\/strong>, <em>1004<\/em>, 178-187. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molstruc.2011.08.002\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.molstruc.2011.08.002<\/a><\/p>\r\n<p>Sayin S., Akkus G. U., Cibulka R., Stibor I., Yilmaz M: Synthesis of Flavin-Calix[4]arene Conjugate Derivatives. <em>Helv. Chim. Acta<\/em> <strong>2011<\/strong>, <em>94<\/em>, 481-485. <a href=\"http:\/\/dx.doi.org\/10.1002\/hlca.201000260\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/hlca.201000260<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Kafka F., Dvo\u0159\u00e1kov\u00e1 H., Gunnoo S., \u0160anda M., Cibulka R.: Pyrazinium Salts as Efficient Organocatalysts of Mild Oxidations with Hydrogen Peroxide. <em>Adv. Synth. Catal.<\/em> <strong>2011<\/strong>, <em>353<\/em>, 865-870. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201000906\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.201000906<\/a><\/p>\r\n<h3><span class=\"modra0\">2010<\/span><\/h3>\r\n<p>Rohl\u00ed\u010dek J. Cibulka R., Cibulkov\u00e1 J., Maixner J., Hu\u0161\u00e1k M.: 10-Methylisoalloxazine-5-oxide from synchrotron powder diffraction data. <em>Acta Cryst.<\/em> <strong>2010<\/strong>, <em>E66<\/em>, o3350\u2013o3351. <a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536810048932\" target=\"_blank\" rel=\"noopener\">DOI:10.1107\/S1600536810048932<\/a><\/p>\r\n<p>Mojr V., Herzig V., Budesinsky M., Cibulka R., Kraus T.: Flavin-cyclodextrin conjugates as catalysts of enantioselective sulfoxidations with hydrogen peroxide in aqueous media. <em>Chem. Comm.<\/em>, <strong>2010<\/strong>, <em>46<\/em>, 7599\u20137601. <a href=\"http:\/\/dx.doi.org\/10.1039\/C0CC02562C\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C0CC02562C<\/a><\/p>\r\n<p>Kova\u0159\u00ed\u010dek P., Eigner V., Holakovsk\u00fd R.: Ribbon and Pleated Sheet Formation by Anion-Directed Hydrogen Bonding In 1,4-Bis(4,5-dihydro-1<em>H<\/em>-imidazol-2-yl)benzene Salts.<em>Structural Chemistry Communications<\/em>, <strong>2010<\/strong>, <em>Vol. 1<\/em>, <em>No. 1<\/em>, 8-11. <a href=\"http:\/\/www.factumpress.com\/index.php\/scc\/article\/viewFile\/19\/pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/www.factumpress.com\/index.php\/scc\/article\/viewFile\/19\/pdf<\/a><\/p>\r\n<p>Jurok R., Cibulka R., Dvo\u0159\u00e1kov\u00e1 H., Hampl F., Hoda\u010dov\u00e1 J.: Planar Chiral Flavinium Salts - Prospective Catalysts for Enantioselective Sulfoxidation Reactions. <em>Eur. J. Org. Chem.<\/em> <strong>2010<\/strong>, 5217-5224. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201000592\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201000592<\/a><\/p>\r\n<p>Cibulka R.: Flaviny \u2013 perspektivn\u00ed katalyz\u00e1tory oxidac\u00ed a redukc\u00ed. <em>Chem. Listy<\/em> <strong>2010<\/strong>,<em>104<\/em>, 326-333. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/2010_05_326-333.pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/chemicke-listy.cz\/docs\/full\/2010_05_326-333.pdf<\/a><\/p>\r\n<p>J. Budka, V. Eigner, R. Holakovsk\u00fd, P. Kovar\u00edcek and T. Louzilov\u00e1: 25,26,27,28-Tetrapropoxycalix[4]arene-5,17-dicarbonitrile. <em>Acta Cryst.<\/em> <strong>2010<\/strong>, <em>E66<\/em>, o419-o420. <a href=\"http:\/\/journals.iucr.org\/e\/issues\/2010\/02\/00\/om2307\/om2307.pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/journals.iucr.org\/e\/issues\/2010\/02\/00\/om2307\/om2307.pdf<\/a><\/p>\r\n<p>Ji\u0159\u00ed \u017durek, Radek Cibulka, Hana Dvo\u0159\u00e1kov\u00e1, Ji\u0159\u00ed Svoboda: N<sup>1<\/sup>,N<sup>10<\/sup>-Ethylene-bridged flavinium salts derived from <span class=\"kapitalka\">L<\/span>-valinol: synthesis and catalytic activity in H<sub>2<\/sub>O<sub>2<\/sub>oxidations, <em>Tetrahedron Lett.<\/em> <strong>2010<\/strong>, <em>51<\/em>, 1083-1086. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2009.12.096\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.tetlet.2009.12.096<\/a><\/p>\r\n<h3><span class=\"modra0\">2009<\/span><\/h3>\r\n<p>M\u00e9nov\u00e1 P., Eigner V., Cibulka R., \u010cejka J., Dvo\u0159\u00e1kov\u00e1 H.: 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione. <em>Acta Cryst.<\/em> <strong>2009<\/strong>, <em>E65<\/em>, o1536\u2013o1537. <a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536809020856\">DOI:10.1107\/S1600536809020856<\/a><\/p>\r\n<p>Cibulka R., Baxov\u00e1 L., Dvo\u0159\u00e1kov\u00e1 H., Hampl F., M\u00e9nov\u00e1 P., Mojr V., Plancq B., Sayin S.: Catalytic effect of alloxazinium and isoalloxazinium salts on oxidation of sulfides with hydrogen peroxide in micellar media. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2009<\/strong>, <em>74<\/em>, 973-993. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc2009030\">DOI:10.1135\/cccc2009030<\/a><\/p>\r\n<h3><span class=\"modra0\">2008<\/span><\/h3>\r\n<p>Jurok R., Svobodov\u00e1 E., Cibulka R.,Hampl F.: Reactivity in micelles - Are we really able to design micellar catalysts? <em>Collect. Czech. Chem. Commun.<\/em> <strong>2008<\/strong>, <em>73<\/em>, 127-146. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20080127\">DOI:10.1135\/cccc20080127<\/a><\/p>\r\n<h3><span class=\"modra0\">2007<\/span><\/h3>\r\n<p>Baxov\u00e1 L., Cibulka R., Hampl F.: Organocatalytic sulfoxidation in micellar systems containing amphiphilic flavinium salts using hydrogen peroxide as terminal oxidant. <em>J. Mol. Catal. A.<\/em> <strong>2007<\/strong>, <em>277<\/em>, 53\u201360. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molcata.2007.07.027\">DOI:10.1016\/j.molcata.2007.07.027<\/a><\/p>\r\n<p>Cibulka R., Svobodov\u00e1 E., K\u00f6nig B., Ludv\u00edk J., Hampl F., Li\u0161ka F.: Studium vyu\u017eit\u00ed n\u011bkter\u00fdch N-donorov\u00fdch ligand\u016f a jejich komplex\u016f s ionty p\u0159echodn\u00fdch kov\u016f. <em>Chem. Listy<\/em> <strong>2007<\/strong>, <em>101<\/em>, 886-894. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/2007_11_886-894.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/2007_11_886-894.pdf<\/a><\/p>\r\n<h3><span class=\"modra0\">2006<\/span><\/h3>\r\n<p>Celik H., Ekmekci G., Ludv\u00edk J., P\u00edcha J., Zuman P: Electroreduction of aromatic oximes: Diprotonation, adsorption, imine formation, and substituent effects. <em>J. Phys. Chem. B<\/em> <strong>2006<\/strong>, <em>110<\/em>, 6785-6796. <a href=\"http:\/\/dx.doi.org\/10.1021\/jp056808t\">DOI:10.1021\/jp056808t<\/a><\/p>\r\n<p>Kivala M., Cibulka R., Hampl F.: Cleavage of 4-nitrophenyl diphenyl phosphate by isomeric quaternary pyridinium ketoximes - How can structure and lipophilicity of functional surfactants influence their reactivity in micelles and microemulsions?<em>Collect. Czech. Chem. Commun.<\/em> <strong>2006<\/strong>, <em>71<\/em>, 1642-1658. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20061642\">DOI:10.1135\/cccc20061642<\/a><\/p>\r\n<h3><span class=\"modra0\">2005<\/span><\/h3>\r\n<p>Svobodov\u00e1 E., Cibulka R., Hampl F., \u0160midrkal J., Li\u0161ka F.: Metal ion transport through bulk liquid membrane mediated by cationic ligand surfactants. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2005<\/strong>, <em>70<\/em>, 441-465. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20050441\">DOI:10.1135\/cccc20050441<\/a><\/p>\r\n<p>Chvapil M., Kielar F., Li\u0161ka F., \u0160ilh\u00e1nkov\u00e1 A., Bregel K.: Synthesis and evaluation of long-acting d-penicillamine derivatives. <em>Connective Tissue Research<\/em> <strong>2005<\/strong>, <em>46<\/em>, 242-250. <a href=\"http:\/\/dx.doi.org\/10.1080\/03008200500416690\">DOI:10.1080\/03008200500416690<\/a><\/p>\r\n<p>P\u00edcha J., Ku\u010da K., Kivala M., Kohout M., Cabal J., Li\u0161ka F.: A new group of monoquaternary reactivators of acetylcholinesterase inhibited by nerve agents. <em>J. Enzyme Inhib. Med. Chem.<\/em> <strong>2005<\/strong>, <em>20<\/em>, 233-237. <a href=\"http:\/\/dx.doi.org\/10.1080\/14756360400021858\">DOI:10.1080\/14756360400021858<\/a><\/p>\r\n<h3><span class=\"modra0\">2004<\/span><\/h3>\r\n<p>P\u00edcha J., Cibulka R., Hampl F., Li\u0161ka F., Pa\u0159\u00edk P., Pytela O.: Reactivity of p-substituted benzaldoximes in the cleavage of <em>p<\/em>-nitrophenyl acetate: kinetic and mechanism.<em>Collect. Czech. Chem. Commun.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 397-413. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20040397\">DOI:10.1135\/cccc20040397<\/a><\/p>\r\n<p>P\u00edcha J., Cibulka R., Li\u0161ka F., Pa\u0159\u00edk P., Pytela O.: Reparametrization and\/or determination of Hammett, inductive, mesomeric and AISE substituent constants for five substituents: N<sup>+<\/sup>(CH<sub>3<\/sub>)<sub>3<\/sub>, CH<sub>2<\/sub>N<sup>+<\/sup>(CH<sub>3<\/sub>)<sub>3<\/sub>, CH<sub>2<\/sub>Py, CH<sub>2<\/sub>SO<sub>2<\/sub>CH<sub>3<\/sub> and PO(OCH<sub>3<\/sub>)<sub>2<\/sub>.<em>Collect. Czech. Chem. Commun.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 2239-2252. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20042239\">DOI:10.1135\/cccc20042239<\/a><\/p>\r\n<p>Wiest O., Harrison C. B., Saettel N. J., Cibulka R., Sax M., K\u00f6nig B.: Design, synthesis and evaluation of a biomimetic artificial photolyase model. <em>J. Org. Chem.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 8183\u20138185. <a href=\"http:\/\/dx.doi.org\/10.1021\/jo0494329\">DOI:10.1021\/jo0494329<\/a><\/p>\r\n<p>Cibulka R., Vasold R. K\u00f6nig B.: Catalytic Photooxidation of 4-Methoxybenzyl alcohol with Flavin Zinc(II) cyclen complex. <em>Chem. Eur. J.<\/em> <strong>2004<\/strong>, <em>10<\/em>, 6223\u20136231. <a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200400232\">DOI:10.1002\/chem.200400232<\/a><\/p>\r\n<h3><span class=\"modra0\">2002<\/span><\/h3>\r\n<p>Ludvik J., Cibulka R.: Electroreduction of methyl azinyl ketoximes and their Ni(II), Cu(II) and Zn(II) complexes on mercury - correlation with their hydrolytic activity. Proceedings of the Fifth International Manuel M. Baizer Symposium in Honor of Professor Jean Michel Saveant, The 201th Meeting of the Electrochemical Society<strong>2002<\/strong>, Vol. 10, p. 142\u2013146.<\/p>\r\n<h3><span class=\"modra0\">2001<\/span><\/h3>\r\n<p>Cibulka R., C\u00edsa\u0159ov\u00e1 I., Ondr\u00e1\u010dek J., Li\u0161ka F., Ludv\u00edk J.: Electrochemical Reductions of Ni<sup>2+<\/sup>, Cu<sup>2+<\/sup> and Zn<sup>2+<\/sup> Complexes of Azinyl Methyl Ketoximes on Mercury. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2001<\/strong>, <em>66<\/em>, 170. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20010170\">DOI:10.1135\/cccc20010170<\/a><\/p>\r\n<p>Kotou\u010dov\u00e1 H., Cibulka R., Hampl F., Li\u0161ka F.: Amphiphilic quaternary pyridinium ketoximes as functional hydrolytic micellar catalysts \u2013 does the nucleophilic function position influence their reactivity? <em>J. Mol. Catal.<\/em>, <strong>2001<\/strong>, <em>174<\/em>, 59. <a href=\"http:\/\/dx.doi.org\/10.1016\/S1381-1169(01)00178-9\">DOI:10.1016\/S1381-1169(01)00178-9<\/a><\/p>\r\n<p>Ml\u00ed\u010dkov\u00e1 K., \u0160ebela M., Cibulka R., Fr\u00e9bort I., Pe\u010d P., Li\u0161ka F., Tanizawa K.: Inhibition of copper amine oxidases by pyridine-derived aldoximes and ketoximes. <em>Biochimie <\/em><strong>2001<\/strong>, <em>83<\/em>(11-12), 995\u20131002. <a href=\"http:\/\/dx.doi.org\/10.1016\/S0300-9084(01)01345-1\">DOI:10.1016\/S0300-9084(01)01345-1<\/a><\/p>\r\n<p>Cibulka R., Hampl F., Kotou\u010dov\u00e1 H., P\u00e1v O., \u0160ilh\u00e1nkov\u00e1 A., Li\u0161ka F.: Quaternary ketoximes \u2013 New perspective compounds for hydrolysis of toxic organophosphates.<em>Vojensk\u00e9 zdrav. Listy \u2013 Suplementum-<\/em> <strong>2001<\/strong>, <em>70<\/em>(1), 38\u201340.<\/p>\r\n<p>Cibulka R.: Hydrolytick\u00e9 katalyz\u00e1tory zalo\u017een\u00e9 na komplexech alkyl(pyridin-2-yl)ketoxim\u016f. <em>Chem. Listy<\/em> <strong>2001<\/strong>, <em>95<\/em>, 809\u2013810. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/archiv\/2001\/12-PDF\/809-810.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/archiv\/2001\/12-PDF\/809-810.pdf<\/a><\/p>\r\n<h3><span class=\"modra0\">2000<\/span><\/h3>\r\n<p>Cibulka R., Hampl F., Kotou\u010dov\u00e1 H., Maz\u00e1\u010d J., Li\u0161ka F.: Quaternary pyridinium ketoximes \u2013 New efficient micellar hydrolytic catalysts. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 227. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20000227\">DOI:10.1135\/cccc20000227<\/a><\/p>\r\n<p>Cibulka R., Li\u0161ka F., Ludv\u00edk J.: Electrochemical reductions of methyl azinyl ketoximes on mercury. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 1630. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20001630\">DOI:10.1135\/cccc20001630<\/a><\/p>\r\n<h3><span class=\"modra0\">1999<\/span><\/h3>\r\n<p>Cibulka R., Hampl F., \u0160midrkal J. and Li\u0161ka F.: Lipophilic N-[2-hydroxyimino-2-(pyridin-2-yl)ethyl]tialkylammonium salts \u2013 New ligands for metal ion extractions into organic solvents, <em>Tetrahedron Lett.<\/em> <strong>1999<\/strong>, <em>40<\/em>, 6849. <a href=\"http:\/\/dx.doi.org\/10.1016\/S0040-4039(99)01382-9\">DOI:10.1016\/S0040-4039(99)01382-9<\/a><\/p>\r\n<p>Cibulka R., Hampl F., Martinu T., Mazac J., Totevova S., Liska F.: Metal ion chelates of lipophilic alkyl diazinyl ketoximes as hydrolytic catalysts <em>Collect. Czech. Chem. Commun.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 1159. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc19991159\">DOI:10.1135\/cccc19991159<\/a><\/p>\r\n<h3><span class=\"modra0\">1998<\/span><\/h3>\r\n<p>Cibulka R., Hampl F., Li\u0161ka F.: P\u0159\u00edprava a vyu\u017eit\u00ed amfifiln\u00edch oxim\u016f odvozen\u00fdch od azin\u016f, <em>Chem. listy<\/em> <strong>1998<\/strong>, <em>92(6)<\/em>, 469. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/1998_06_469-474.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/1998_06_469-474.pdf<\/a><\/p>\r\n<p>Kotou\u010dov\u00e1 H., Maz\u00e1\u010d J., Cibulka R., Hampl F. and Li\u0161ka F: Unusual course of the p-nitrophenyl phosphate esters cleavage by 3-hydroxyiminoalkylpyridinium salts in micellar solutions, <em>Chem. Lett.<\/em> <strong>1998<\/strong> <em>(7)<\/em>, 649. <a href=\"http:\/\/dx.doi.org\/10.1246\/cl.1998.649\">DOI:10.1246\/cl.1998.649<\/a><\/p>\r\n<h3><span class=\"modra0\">1997<\/span><\/h3>\r\n<p>Cibulka R., Dvo\u0159\u00e1k D., Hampl F., Li\u0161ka F.: Metallomicellar hydrolytic catalysts containing ligand surfactants derived from alkyl-2-pyridinylketoxime, <em>Collect. Czech. Chem. Commun.<\/em> <strong>1997<\/strong>, <em>62<\/em>, 1342. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc19971342\">DOI:10.1135\/cccc19971342<\/a><\/p>\r\n<p><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["15408","136690","136692"],"poduzly_count":3,"poduzly_count_aut":2,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. 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src=\"\/images\/0!0\/uzel\/0136669\/0068~~K87JTEktUkjOTCrNyU5USM0DAA.png\" alt=\" \u25f3 slider cibulka en (png) \u2192 (origin\u00e1l)\" width=\"823\" height=\"200\"><\/p>\r\n<p>Bou\u0161kov\u00e1 T.: Konjug\u00e1ty porfyrin\u016f a flavinem jako potenci\u00e1ln\u00ed \u010dinidla pro fotodynamickou terapii (2026).<\/p>\r\n<p>Abdelfattah Z.: Anionty odvozen\u00e9 od naftalenov\u00fdch analog\u016f alloxazin\u016f jako potenci\u00e1ln\u00ed fotoredoxn\u00ed katalyz\u00e1tory (2025).<\/p>\r\n<p>Rozmu\u0161ov\u00e1 M.: N-dealkylace amin\u016f \u0159\u00edzen\u00e1 viditeln\u00fdm sv\u011btlem prost\u0159ednictv\u00edm flavinov\u00e9 fotokatal\u00fdzy (2025).<\/p>\r\n<p>\u0158eh\u00e1\u010dek J.: Synt\u00e9za a vyu\u017eit\u00ed aniontu odvozen\u00e9ho od 8-hydroxyisoalloxazinu a 8-sulfanylisoalloxazinu jako redoxn\u00edho fotokatalyz\u00e1toru (2025).<\/p>\r\n<p>Semeck\u00fd J.:&nbsp;<span>Flavinov\u00e9 anionty ve fotoredoxn\u00ed katal\u00fdze (2024).<\/span><\/p>\r\n<p>M\u00edkov\u00e1 P.: <span>Deazaflavins immobilized on mesoporous silica for photoreductions (2022).<\/span><\/p>\r\n<p>Zubova E.: <span>Interaction of flavin derivatives with nucleophiles as a tool for organocatalytic umpolung (2022).<\/span><\/p>\r\n<p><span>Ml\u010dochov\u00e1 A.: Chir\u00e1ln\u00ed ligandy pro interakci s anionty (2021).<\/span><\/p>\r\n<p><span>Nademlejnsk\u00e1 K.: Konjug\u00e1ty porfyrin\u016f s flavinem a modelem NADH (2021).<\/span><\/p>\r\n<p><span>Weisheitelov\u00e1 I.: Flaviny s n\u00e1sobnou vazbou v postrann\u00edm \u0159et\u011bzci (2021).<\/span><\/p>\r\n<p><span>Wohlr\u00e1bov\u00e1 L.: BODIPY substituovan\u00e9 sulfonothio\u00e1ty: nov\u00e9 fotoodstupiteln\u00e9 chr\u00e1nic\u00ed skupiny pro aktivaci viditeln\u00fdm sv\u011btlem (2021).<\/span><\/p>\r\n<p>Copko J.:&nbsp; <span>Synt\u00e9za analog\u016f prenylflavinu a jejich vyu\u017eit\u00ed ve fotokatal\u00fdze (2020).<\/span><\/p>\r\n<p>Jank\u016f K.: Mo\u010doviny na b\u00e1zi binaftalenu pro enantioselektivn\u00ed interakce (2018).<\/p>\r\n<p>Nevesel\u00fd T.: Deriv\u00e1ty flavin\u016f pro fotokatalytick\u00e9 redukce (2018).<\/p>\r\n<p>Pokluda A.: Nov\u00e9 reagenty pro Mitsunobuovu reakci (2018).<\/p>\r\n<p>\u0160pa\u010dkov\u00e1 J.: Elektronov\u011b deficitn\u00ed flaviniov\u00e9 soli pro fotokatalytick\u00e9 oxidace (2018).<\/p>\r\n<p>Valenta L.: Nov\u00e9 syst\u00e9my pro fotokatalytickou Mitsunobuovu reakci (2018).<\/p>\r\n<p>H\u00e1jek P.: Ligandy na b\u00e1zi binaftalenu pro enantioselektivn\u00ed komplexaci chir\u00e1ln\u00edch slou\u010denin (2016).<\/p>\r\n<p>Jir\u00e1sek M.: Organokatalytick\u00e9 [2+2] fotocykloadice dien\u016f obsahuj\u00edc\u00edch atom dus\u00edku (2016).<\/p>\r\n<p>Strakov\u00e1 K.: Transformace aktivovan\u00fdch alken\u016f na nenasycen\u00e9 sulfony nebo cyklobutany s vyu\u017eit\u00edm fotokatal\u00fdzy a viditeln\u00e9ho sv\u011btla (2016).<\/p>\r\n<p>Jakubec M.: P\u0159\u00edprava chir\u00e1ln\u00edch flavin\u016f s helicenovou jednotkou (2015).<\/p>\r\n<p>Just D.: Cyklick\u00e9 ligandy na b\u00e1zi binaftalenov\u00fdch mo\u010dovin pro enantioselektivn\u00ed komplexaci (2015).<\/p>\r\n<p>Zelenka J.:&nbsp;Synt\u00e9za flavinov\u00fdch katalyz\u00e1tor\u016f na b\u00e1zi disubstituovan\u00e9ho \u03b2-cyklodextrinu (2015).<\/p>\r\n<p>Zvon\u00ed\u010dek V.: Synt\u00e9za a studium pyridaziniov\u00fdch a triaziniov\u00fdch sol\u00ed jako katalyz\u00e1tor\u016f oxidac\u00ed (2015).<\/p>\r\n<p>Hartman T.: Kvartern\u00ed heteroareniov\u00e9 soli jako katalyz\u00e1tory oxidac\u00ed v dvouf\u00e1zov\u00e9m prost\u0159ed\u00ed (2014).<\/p>\r\n<p>Koll\u00e1r O.: P\u0159\u00edprava enantiomern\u011b \u010dist\u00fdch 1,1\u2018-binaftalen\u016f nesouc\u00edch v poloh\u00e1ch 2- a 2\u2018- alespo\u0148 jednu karboxylovou skupinu (2014).<\/p>\r\n<p>Kos M.: 3-[2-(Dialkylamino)ethoxy]-4-(hydroxyiminomethyl)pyridiniov\u00e9 soli jako nov\u00e9 reaktiv\u00e1tory acetylcholinesterasy (2014).<\/p>\r\n<p>M\u00e4rz M.: Ligandy na b\u00e1zi binaftalenu pro enantioselektivn\u00ed komplexace sulfoxid\u016f (2014).<\/p>\r\n<p>Tomanov\u00e1 P.: Synt\u00e9za a studium katalyz\u00e1tor\u016f na b\u00e1zi alloxazin-cyklodextrinov\u00fdch konjug\u00e1t\u016f p\u0159ipraven\u00fdch [3+2] cykloadic\u00ed (2014).<\/p>\r\n<p>Boh\u00e1\u010dov\u00e1 S.: Kvartern\u00ed pyridiniov\u00e9 soli jako katalyz\u00e1tory oxidac\u00ed peroxidem vod\u00edku (2013).<\/p>\r\n<p>Kala M.: 3-[\u03c9-(Dialkylamino)alkyl]pyridin-4-aldoximy jako prekurzory reaktiv\u00e1tor\u016f acetylcholinesterasy (2013).<\/p>\r\n<p>Ma\u0148\u00e1skov\u00e1 K.: Nov\u00e9 reaktiv\u00e1tory acetylcholinesterasy odvozen\u00e9 od pralidoximu (2013).<\/p>\r\n<p>Mik\u0161\u00e1tko J.: P\u0159\u00edprava a rentgenostrukturn\u00ed anal\u00fdza heterocyklick\u00fdch amidin\u016f (2012).<\/p>\r\n<p>Da\u010fov\u00e1 J.: Synt\u00e9za deriv\u00e1t\u016f flavinu a jejich vyu\u017eit\u00ed p\u0159i fotooxidac\u00edch (2011).<\/p>\r\n<p>Kone\u010dkov\u00e1 E.: Katalyz\u00e1tory na b\u00e1zi thiomo\u010doviny pro sulfoxida\u010dn\u00ed reakce (2011).<\/p>\r\n<p>Herzig V.: Synt\u00e9za konjug\u00e1t\u016f isoalloxazinu a cyklodextrinu a jejich vyu\u017eit\u00ed jako katalyz\u00e1tor\u016f enantioselektivn\u00edch oxidac\u00ed sulfid\u016f (2011).<\/p>\r\n<p>\u0160turala J.: Synt\u00e9za Tr\u00f6gerov\u00fdch baz\u00ed s flavinovou podjednotkou (2011).<\/p>\r\n<p>Cigl M.: Nov\u00e9 kapaln\u00e9 krystaly s later\u00e1ln\u00ed substituc\u00ed j\u00e1dra (2010).<\/p>\r\n<p>Eigner V.: Isothiouroniov\u00e9 soli jako stavebn\u00ed bloky pro krystalov\u00e9 struktury (2010).<\/p>\r\n<p>Kova\u0159\u00ed\u010dek P.: Amidiny pro koordina\u010dn\u00ed a supramolekul\u00e1rn\u00ed chemii (2010).<\/p>\r\n<p>M\u00e9nov\u00e1 P.: Studium vlastnost\u00ed flaviniov\u00fdch sol\u00ed a jejich C4a-adukt\u016f (2010).<\/p>\r\n<p>Mojr V.: Katalyz\u00e1tory oxida\u010dn\u00edch reakc\u00ed na b\u00e1zi konjug\u00e1t\u016f flavinu a cyklodextrinu (2010).<\/p>\r\n<p>Kafka F.: Pyraziniov\u00e9 a dihydropyraziniov\u00e9 soli jako modely deriv\u00e1t\u016f flavinu (2008).<\/p>\r\n<p>Sl\u00e1dkov\u00e1 M.: Isothiouroniov\u00e9 soli jako ligandy pro interakci s anionty (2008).<\/p>\r\n<p>\u0160\u00e1mal M.: Synt\u00e9za nov\u00fdch kapaln\u00fdch krystal\u016f na b\u00e1zi ortho-substituovan\u00fdch 4-alkoxyfenyl-4-alkoxybenzo\u00e1t\u016f (2008).<\/p>\r\n<p>Baxov\u00e1 L.: Synt\u00e9za a studium amfifiln\u00edch flaviniov\u00fdch sol\u00ed jako katalyz\u00e1tory oxidace sulfid\u016f v micel\u00e1rn\u00edch roztoc\u00edch (2007).<\/p>\r\n<p>Jurok R.: Synt\u00e9za nov\u00fdch kapaln\u00fdch krystal\u016f s bifenylov\u00fdm j\u00e1drem s later\u00e1ln\u00ed substituc\u00ed (2007).<\/p>\r\n<p>K\u0159ov\u00e1\u010dek M.: Vliv lipofiln\u00edch supernukleofil\u016f na pr\u016fb\u011bh hydrol\u00fdzy model\u016f toxick\u00fdch organofosf\u00e1t\u016f a fosfon\u00e1t\u016f v micel\u00e1ch kationick\u00fdch tenzid\u016f (2004).<\/p>\r\n<p>Kivala M.: Studium hydrol\u00fdzy difenyl-(4-nitrofenyl)-fosf\u00e1tu \u00fa\u010dinkem kvartern\u00edch pyridiniov\u00fdch ketoxim\u016f v r\u016fzn\u00fdch typech micel\u00e1rn\u00edch roztok\u016f a v mikroemulz\u00edch o\/v (2003).<\/p>\r\n<p>Koz\u00e1kov\u00e1 M.: Synt\u00e9za a hydrolytick\u00e1 \u00fa\u010dinnost amfifiln\u00edch kvartern\u00edch heteroareniov\u00fdch ketoxim\u016f (2003).<\/p>\r\n<p>R\u00f6dling R.: <sup>31<\/sup>P NMR studium hydrol\u00fdzy difenyl-(4-nitrofenyl)fosf\u00e1tu v micel\u00e1ch kvart\u00e9rn\u00edch pyridiniov\u00fdch oxim\u016f (2002).<\/p>\r\n<p>Han\u00e1\u010dkov\u00e1 E.: Nov\u00e9 amfifiln\u00ed pyridinov\u00e9 ligandy pro transport iont\u016f p\u0159es kapalnou membr\u00e1nu (2001).<\/p>\r\n<p>Ku\u010da K.: Synt\u00e9za a studium \u00fa\u010dinnosti micel\u00e1rn\u00edch hydrolytick\u00fdch katalyz\u00e1tor\u016f na b\u00e1zi kvart\u00e9rn\u00edch isochinoliniov\u00fdch ketoxim\u016f (2001).<\/p>\r\n<p>P\u00e1v O.: Kvartern\u00ed chinoliniov\u00e9 oximy - potenci\u00e1ln\u00ed micel\u00e1rn\u00ed hydrolytick\u00e9 katalyz\u00e1tory (2001).<\/p>\r\n<p>\u0160midrkal J.: Transport iont\u016f p\u0159es kapaln\u00e9 membr\u00e1ny pomoc\u00ed lipofiln\u00edch N,N-dialkyl-N[2-hydroxyimino-2-(pyridin-2-yl)ethyl]-dialkylamoniov\u00fdch sol\u00ed (2000).<\/p>\r\n<p>Martin\u016f T.: Synt\u00e9za azinylmethylketoxim\u016f a NMR studium jejich komplex\u016f s ionty p\u0159echodn\u00fdch kov\u016f (1998).<\/p>\r\n<p>Kotou\u010dov\u00e1 H.: Kvart\u00e9rn\u00ed pyridiniov\u00e9 ketoximy jako micel\u00e1rn\u00ed hydrolytick\u00e9 katalyz\u00e1tory (1997).<\/p>\r\n<p>Petrl\u00edkov\u00e1 \u0160.: Synt\u00e9za pyridaziniov\u00fdch karbaldoxim\u016f - potenci\u00e1ln\u00edch reaktiv\u00e1tor\u016f fosfonylovan\u00e9 acetylcholinesterasy (1997).<\/p>\r\n<p>Cibulka R.: Amfifiln\u00ed komplexy odvozen\u00e9 od pyridinu (1996).<\/p>\r\n<p>Vo\u0161tov\u00e1 S.: Synt\u00e9za a vlastnosti ligand\u016f na b\u00e1zi alkyl-3-pyridazinylketoxim\u016f (1995).<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["15408","136691"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. 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M.: Kapaln\u011b-krystalick\u00e9 molekul\u00e1rn\u00ed p\u0159ep\u00edna\u010de (2017).<\/p>\r\n<p>\u0160turala J.: Heteroareniov\u00e9 soli jako katalyz\u00e1tory oxida\u010dn\u00edch reakc\u00ed (2016).<\/p>\r\n<p>Kotou\u010dov\u00e1 H.: Stereoselektivn\u00ed a chemoselektivn\u00ed oxidace s vyu\u017eit\u00edm flaviniov\u00fdch sol\u00ed (2015).<\/p>\r\n<p>Jurok R.: Stericky br\u00e1n\u011bn\u00e9 deriv\u00e1ty flavinu (2013).<\/p>\r\n<p>\u017durek J.: Enantioselektivn\u00ed Organokatalyz\u00e1tory odvozen\u00e9 od flaviniov\u00fdch sol\u00ed (2012).<\/p>\r\n<p>Svobodov\u00e1 E.: Synt\u00e9za a studium vlastnost\u00ed amfifiln\u00edch ligand\u016f (2006).<\/p>\r\n<p>P\u00edcha J.: Oximy jako katalyz\u00e1tory hydrol\u00fdzy ester\u016f (2006).<\/p>\r\n<p>Sl\u00e1\u010dalov\u00e1 K.: Reaktiv\u00e1tory acetylcholinesterasy (2003).<\/p>\r\n<p>Cibulka R.: Elektrochemick\u00e9 a spektroskopick\u00e9 studium komplex\u016f alkyl(azinyl)ketoxim\u016f (2002).<\/p>\r\n<p>Maz\u00e1\u010d J.: Synt\u00e9za a studium \u00fa\u010dinnosti micel\u00e1rn\u00edch hydrolytick\u00fdch katalyz\u00e1tor\u016f (1996).<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["15408","136693"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. 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&nbsp; &nbsp;&nbsp;<span class=\"cervena0\"><span class=\"cerna0\"><a href=\"\/\/uoch-r.vscht.cz\/research\/cibulka\/lide\/cibulka\" target=\"_blank\" rel=\"noopener\">(CV)<\/a><\/span><\/span><span class=\"cervena0\"><span class=\"cerna0\"><br><\/span><\/span><\/li>\r\n<li>Ing. <strong>Eva Svobodov\u00e1<\/strong>, Ph.D.&nbsp;&nbsp;&nbsp; <a href=\"\/\/uoch-r.vscht.cz\/research\/cibulka\/lide\/136701\" target=\"_blank\" rel=\"noopener\">(CV)<\/a><\/li>\r\n<li>Mgr. <strong>Roman Holakovsk\u00fd<\/strong>, Ph.D.&nbsp;&nbsp;&nbsp; <a href=\"\/\/uoch-r.vscht.cz\/research\/cibulka\/lide\/136700\" target=\"_blank\" rel=\"noopener\">(CV)<\/a><\/li>\r\n<li>Dr. <strong>Tetiana Pavlovska<\/strong> (post-doc)<\/li>\r\n<li>Dr. <strong>Dorian Dupommier<\/strong> (post-doc)<\/li>\r\n<li><strong>Martina Kovandov\u00e1<\/strong><\/li>\r\n<\/ul>\r\n<h2><span class=\"modra0\">Ph.D. students<\/span><\/h2>\r\n<ul>\r\n<li>Ing. Ekaterina Zubova<\/li>\r\n<li>Ing. Rostislav Sponar<\/li>\r\n<li>Ing. Jakub Semeck\u00fd<\/li>\r\n<li>Ing. Marie Rozmu\u0161ov\u00e1<\/li>\r\n<\/ul>\r\n<h2><span class=\"modra0\">Students<\/span><\/h2>\r\n<ul>\r\n<li>Viktor Vojan<\/li>\r\n<li>Krist\u00fdna \u0160oltov\u00e1<\/li>\r\n<li>Kate\u0159ina Riegerov\u00e1<\/li>\r\n<li>Barbora Z\u00edtkov\u00e1<\/li>\r\n<li>Jaroslav Jur\u00e1k<\/li>\r\n<\/ul>\r\n<h2><span class=\"modra0\">Collaboration<\/span><\/h2>\r\n<ul>\r\n<li>Prof. Marek Sikorski (Laborato\u0159 fotofyziky, Univerzita v Poznani)<\/li>\r\n<li>Prof. Ji\u0159\u00ed Ludv\u00edk (\u00dastav fyzik\u00e1ln\u00ed chemie J. Heyrovsk\u00e9ho, AV \u010cR)<\/li>\r\n<li>Prof. Burkhard K\u00f6nig (Univerzita Regensburg, N\u011bmecko)<\/li>\r\n<li>Dr. Ullrich Jahn (\u00dastav organick\u00e9 chemie a biochemie, AV \u010cR)<\/li>\r\n<li>Dr. Roger-Jan Kutta&nbsp;(Univerzita Regensburg, N\u011bmecko)<\/li>\r\n<li>Dr. Tom\u00e1\u0161 Slanina (\u00dastav organick\u00e9 chemie a biochemie, AV \u010cR)&nbsp;<\/li>\r\n<\/ul>\r\n<h2><\/h2>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["139488","136695","136696","136697","136698","15408","136699","136700","136701"],"poduzly_count":9,"poduzly_count_aut":4,"poduzly":{"poduzly_count_aut_sum":0,"139488":{"idvazba":"171594","nad_uzel":"136694","pod_uzel":"139488","url":"\/research\/cibulka\/lide\/139488","sablona":"58","nazev":"Guests","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/lide\/139488}","poradi":"0","skupina_www":"everyone","platne_od":"11.06.2026 10:44:00","platne_do":null,"iduzel":"139488","obsah":"a:14:{s:5:\"nazev\";s:6:\"Guests\";s:9:\"seo_title\";s:6:\"Guests\";s:8:\"seo_desc\";s:6:\"Guests\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:1124:\"<p><img src=\"\/images\/0!0\/uzel\/0136669\/0068~~K87JTEktUkjOTCrNyU5USM0DAA.png\" alt=\" \u25f3 slider cibulka en (png) \u2192 (origin\u00e1l)\" width=\"823\" height=\"200\"><\/p>\r\n<ul>\r\n<li>Marina Oka (Japonsko, 2024)<\/li>\r\n<li>Sven St\u00f6ver (N\u011bmecko, 2023)<\/li>\r\n<li>Ester Sans Panades (\u0160pan\u011blsko, 2021)<\/li>\r\n<li>Vincent George (N\u011bmecko, 2019)<\/li>\r\n<li>Dharmik Gadhiya (Polsko, 2019)<\/li>\r\n<li>Killiann Heinz (Francie, 2019, 2020)<\/li>\r\n<li>Camille Tribout (Francie, 2018)<\/li>\r\n<li>Thibaud Bailly (Francie, 2017)<\/li>\r\n<li>Jehanne Grimmer (Francie, 2017)<\/li>\r\n<li>Sarah Bailly (Francie, 2017)<\/li>\r\n<li>Guillaume Hoffmann (Francie, 2016)<\/li>\r\n<li>Dr. Dorota Prukala (Polsko, 2014, 2015)<\/li>\r\n<li>Nadia Ryter (\u0160v\u00fdcarsko, 2010)<\/li>\r\n<li>Smita Gunnoo (Velk\u00e1 Brit\u00e1nie, 2008)<\/li>\r\n<li>Andreja \u010condor (Chorvatsko, 2007)<\/li>\r\n<li>Serkan Sayin (Turecko, 2007)<\/li>\r\n<li>Jenna Scotcher (Velk\u00e1 Brit\u00e1nie, 2006)<\/li>\r\n<li>Baptiste Plancq (Francie, 2005)<\/li>\r\n<li>Markus W. Kriegl (Rakousko, 2005)<\/li>\r\n<li>Tilman Schulz (N\u011bmecko, 2004)<\/li>\r\n<li>Yuliya Milaslavina (B\u011blorusko, 2002)<\/li>\r\n<li>Rina Matsumi (Japonsko, 2001)<\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136695":{"idvazba":"168140","nad_uzel":"136694","pod_uzel":"136695","url":"","sablona":"11","nazev":"Zam\u011bstnanci","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"13.05.2026 07:57:11.888338","platne_do":null,"iduzel":"136695","obsah":"a:1:{s:6:\"nadpis\";s:12:\"Zam\u011bstnanci\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136696":{"idvazba":"168141","nad_uzel":"136694","pod_uzel":"136696","url":"","sablona":"11","nazev":"Ph.D. Studenti","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"13.05.2026 07:57:12.288378","platne_do":null,"iduzel":"136696","obsah":"a:4:{s:6:\"nadpis\";s:14:\"Ph.D. Studenti\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136697":{"idvazba":"168142","nad_uzel":"136694","pod_uzel":"136697","url":"","sablona":"11","nazev":"Konference","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"13.05.2026 07:57:13.029097","platne_do":null,"iduzel":"136697","obsah":"a:4:{s:6:\"nadpis\";s:10:\"Konference\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136698":{"idvazba":"168143","nad_uzel":"136694","pod_uzel":"136698","url":"","sablona":"11","nazev":"Mimo\u0161koln\u00ed aktivity","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"13.05.2026 07:57:14.123553","platne_do":null,"iduzel":"136698","obsah":"a:1:{s:6:\"nadpis\";s:27:\"Na\u0161e mimo\u0161koln\u00ed aktivity\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"15408":{"idvazba":"168144","nad_uzel":"136694","pod_uzel":"15408","url":"","sablona":"4","nazev":"prof. Cibulka research group","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"10.06.2026 11:19:00","platne_do":null,"iduzel":"15408","class":"infobox","autonomni":"0","pod_uzly":["15431","15431","15431","15414","15414","15414","16013","16013","16013","15412","15412","15412","15413","15413","15413"],"poduzly_count":15,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"15431":{"idvazba":"18864","nad_uzel":"15408","pod_uzel":"15431","url":"","sablona":null,"nazev":"Home","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 14:39:00","platne_do":null,"iduzel":"15431","obsah":"a:4:{s:4:\"akce\";s:4:\"Home\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:17:\"\/research\/cibulka\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15414":{"idvazba":"18838","nad_uzel":"15408","pod_uzel":"15414","url":"","sablona":null,"nazev":"People","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"07.06.2026 20:57:00","platne_do":null,"iduzel":"15414","obsah":"a:4:{s:4:\"akce\";s:6:\"People\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:22:\"\/research\/cibulka\/lide\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"16013":{"idvazba":"19734","nad_uzel":"15408","pod_uzel":"16013","url":"","sablona":null,"nazev":"Research","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"07.06.2026 20:59:00","platne_do":null,"iduzel":"16013","obsah":"a:4:{s:4:\"akce\";s:8:\"Research\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:24:\"\/research\/cibulka\/Vyzkum\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15412":{"idvazba":"18836","nad_uzel":"15408","pod_uzel":"15412","url":"","sablona":null,"nazev":"Publications","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"07.06.2026 20:58:00","platne_do":null,"iduzel":"15412","obsah":"a:4:{s:4:\"akce\";s:12:\"Publications\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:27:\"\/research\/cibulka\/publikace\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0},"15413":{"idvazba":"18837","nad_uzel":"15408","pod_uzel":"15413","url":"","sablona":null,"nazev":"Projects","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"07.06.2026 20:58:00","platne_do":null,"iduzel":"15413","obsah":"a:4:{s:4:\"akce\";s:8:\"Projects\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:24:\"\/research\/cibulka\/granty\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0}}},"136699":{"idvazba":"170887","nad_uzel":"136694","pod_uzel":"136699","url":"\/research\/cibulka\/lide\/cibulka","sablona":"58","nazev":"Prof. Ing. Radek Cibulka, Ph.D.","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/lide\/cibulka}","poradi":"6","skupina_www":"everyone","platne_od":"13.07.2026 13:38:00","platne_do":null,"iduzel":"136699","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:31:\"Prof. Ing. Radek Cibulka, Ph.D.\";s:8:\"seo_desc\";s:31:\"Prof. Ing. Radek Cibulka, Ph.D.\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:676:\"<p><img src=\"\/images\/0!0\/uzel\/0136699\/0001~~C0pMSc1WcM5MKs3JTgQA.png\" class=\"img_float_right\" alt=\" \u25f3 Radek Cibulka (png) \u2192 (origin\u00e1l)\" width=\"220\" height=\"249\"><\/p>\r\n<h2 style=\"text-align: center;\"><\/h2>\r\n<h2 style=\"text-align: center;\">Curriculum Vitae<\/h2>\r\n<h2 style=\"text-align: center;\"><strong><span class=\"modra0\">Prof. Radek Cibulka, Ph.D.<\/span><\/strong><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"modra0\">(ID: H-1298-2016, ORCID ID: 0000-0002-8584-7715)<\/span><\/p>\r\n<p style=\"text-align: center;\"><a href=\"\/files\/uzel\/0136699\/0002~~c85MKs3JTox3MQQA.pdf\" class=\"button_blue_link\">Curriculum Viate<\/a>&nbsp;<\/p>\r\n<p style=\"text-align: left;\"><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136700":{"idvazba":"168146","nad_uzel":"136694","pod_uzel":"136700","url":"\/research\/cibulka\/lide\/136700","sablona":"58","nazev":"Mgr. Roman Holakovsk\u00fd, Ph.D.","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/lide\/136700}","poradi":"7","skupina_www":"everyone","platne_od":"10.06.2026 10:59:00","platne_do":null,"iduzel":"136700","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:29:\"Mgr. Roman Holakovsk\u00fd, Ph.D.\";s:8:\"seo_desc\";s:29:\"Mgr. Roman Holakovsk\u00fd, Ph.D.\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:2232:\"<p><img src=\"\/images\/0!0\/uzel\/0136700\/0001~~C8rPTcxT8MjPSczOLyvOPrwXAA.jpg\" class=\"img_float_right\" alt=\" \u25f3 Roman Holakovsk\u00fd (jpg) \u2192 (origin\u00e1l)\" width=\"215\" height=\"143\"><\/p>\r\n<h2 style=\"text-align: center;\">Odborn\u00fd \u017eivotopis <br>Ing. Roman Holakovsk\u00fd, Ph.D.<\/h2>\r\n<h3 style=\"text-align: center;\">ORCID ID: 0000-0002-9605-4761<br><o:p><\/o:p>ResearcherID: GAO-7274-2022<\/h3>\r\n<h3><strong><\/strong><\/h3>\r\n<h3><strong>Osobn\u00ed data:<\/strong><\/h3>\r\n<p style=\"padding-left: 30px;\"><em>Narozen:<\/em>&nbsp; 6. 6. 1969 v&nbsp;Mlad\u00e9 Boleslavi, \u010cesk\u00e1 Republika<br><em>Rodinn\u00fd stav:&nbsp; <\/em>\u017eenat\u00fd, 3 d\u011bti (nar. 2011, 2014, 2021)<br><em>Vzd\u011bl\u00e1n\u00ed:<\/em>&nbsp; Mgr.: P\u0159\u00edrodov\u011bdeck\u00e1 fakulta Univerzity Karlovy (1992)<br>&nbsp;Ph.D.: Vysok\u00e1 \u0161kola chemicko-technologick\u00e1 v Praze (2001) (Doktorsk\u00e1 diserta\u010dn\u00ed pr\u00e1ce na t\u00e9ma: Enantioselektivn\u00ed&nbsp;&nbsp; reakce).<\/p>\r\n<h3><strong>Odborn\u00fd \u017eivotopis:<\/strong><\/h3>\r\n<p style=\"padding-left: 30px;\"><em>1983-1987<\/em>&nbsp; SP\u0160 chemick\u00e1 v Praze<br><em>1987-1992<\/em>&nbsp; Magistersk\u00e9 studium, P\u0159\u00edrodov\u011bdeck\u00e1 fakulta Univerzity Karlovy<br><em>1992-1994<\/em>&nbsp; zam\u011bstn\u00e1n v \u00dastavu organick\u00e9 chemie a biochemie v&nbsp;Praze<br><em>1994-2001&nbsp; <\/em>Postgradu\u00e1ln\u00ed studium, Vysok\u00e1 \u0161kola chemicko-technologick\u00e1 v Praze pod veden\u00edm prof. I. Stibora<br><em>od roku 2000<\/em>&nbsp; odborn\u00fd asistent, \u00dastav organick\u00e9 chemie, V\u0160CHT Praha<br><em>2002&nbsp; &nbsp;<\/em>zahrani\u010dn\u00ed st\u00e1\u017e na Universit\u00e9 Louis Pasteur ve \u0160trasburku, Francie, profesor Mir&nbsp;Wais&nbsp;Hosseini<br><em>2007<\/em>&nbsp; studijn\u00ed pobyt na Univerzit\u00e9 d\u2018Angers, Francie, profesor Marc Sall\u00e9<\/p>\r\n<h3><strong>Pedagogick\u00e1 \u010dinnost:<\/strong><\/h3>\r\n<p style=\"padding-left: 30px;\">V\u00fduka v p\u0159edm\u011btech Z\u00e1klady farmakochemie, Organick\u00e1 chemie, Laborato\u0159e organick\u00e9 chemie<br>Veden\u00ed bakal\u00e1\u0159sk\u00fdch a diplomov\u00fdch prac\u00ed<\/p>\r\n<h3><strong>V\u00fdzkum: <\/strong><\/h3>\r\n<p style=\"padding-left: 30px;\">Chir\u00e1ln\u00ed ligandy pro enantioselektivn\u00ed komplexace a separace<\/p>\r\n<h3><strong>Publika\u010dn\u00ed \u010dinnost:&nbsp;&nbsp; <\/strong><\/h3>\r\n<p style=\"padding-left: 30px;\">18 origin\u00e1ln\u00edch \u010dl\u00e1nk\u016f, 4 patent, 16 prezentac\u00ed na konferenc\u00edch<\/p>\r\n<p style=\"padding-left: 30px;\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136701":{"idvazba":"168148","nad_uzel":"136694","pod_uzel":"136701","url":"\/research\/cibulka\/lide\/136701","sablona":"58","nazev":"Ing. Eva Svobodov\u00e1, Ph.D.","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/lide\/136701}","poradi":"8","skupina_www":"everyone","platne_od":"10.06.2026 11:11:00","platne_do":null,"iduzel":"136701","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:26:\"Ing. Eva Svobodov\u00e1, Ph.D.\";s:8:\"seo_desc\";s:26:\"Ing. Eva Svobodov\u00e1, Ph.D.\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:2577:\"<h2><strong><img src=\"\/images\/0!0\/uzel\/0136701\/0001~~cy1LVAguy0_KT8kvO7wQAA.jpg\" class=\"img_float_right\" alt=\" \u25f3 Eva Svobodov\u00e1 (jpg) \u2192 (origin\u00e1l)\" width=\"215\" height=\"143\"><br><\/strong><\/h2>\r\n<h2 style=\"text-align: center;\">Curriculum Vitae<\/h2>\r\n<h2 style=\"text-align: center;\"><strong><span class=\"modra0\">Ing. Eva Svobodov\u00e1, Ph.D.<\/span><\/strong><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"modra0\">(ID: AAE-5727-2021, ORCID ID: 0000-0002-4809-2659)<\/span><\/p>\r\n<h2><strong><em>&nbsp;<\/em><\/strong><\/h2>\r\n<p><strong>&nbsp;<\/strong><strong>Personal data:<\/strong><\/p>\r\n<p>Name:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ing. Eva Svobodov\u00e1, Ph.D.<br>Born:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 18.1.1978 in Vset\u00edn, Czech Republic<br>Marital status:&nbsp;&nbsp;&nbsp;&nbsp; married, 2 children (born in 2008 and 2010)<br>e-mail:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <a href=\"mailto:svobodoe@vscht.cz\">svobodoe@vscht.cz<\/a><\/p>\r\n<p><strong>Career Summary:<\/strong><\/p>\r\n<p>1992-1996&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Grammar school in Vset\u00edn, Czech Republic<br>1996-2001&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; M.Sc. with F. Li\u0161ka, University of Chemistry and Technology, Prague, Czech Republic<br>2001-2006&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ph.D. with F. Hampl, University of Chemistry and Technology, Prague, Czech Republic<br>Since 2006&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assistant professor, Department of Organic Chemistry, University of Chemistry and Technology, Prague. Czech&nbsp; Republic<\/p>\r\n<p><strong>Awards:<\/strong><\/p>\r\n<p>The Foundation CURIE BRATISLAVA SIS\u00b403 Award - the best student presentation on 10<sup>th<\/sup> International conference Separation of Ionic Solutes, Podbansk\u00e9, Vysok\u00e9 Tatry, Slovakia, 6 \u2013 11. 9. 2003.<\/p>\r\n<p><strong>Teaching Activity:<\/strong><\/p>\r\n<p>Lectures in Organic chemistry, courses in Laboratory of organic chemistry.<br>Supervising of bachelor and magister thesis.<\/p>\r\n<p><strong>Research Interest:<br><\/strong><\/p>\r\n<p>Chemistry of heterocyclic compounds, flavins and their derivatives, photocatalysis<\/p>\r\n<p><strong>&nbsp;Publication Activity:<\/strong><\/p>\r\n<p>17 original papers in impacted journals, 1 patent, 31 presentations on conferences (author or co-author)<br>H-index: 12<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"136702":{"idvazba":"183715","nad_uzel":"136669","pod_uzel":"136702","url":"\/research\/cibulka\/absolventi","sablona":"49","nazev":"Alumni","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka\/absolventi}","poradi":"12","skupina_www":"everyone","platne_od":"14.07.2026 14:35:00","platne_do":null,"iduzel":"136702","obsah":"a:14:{s:5:\"nazev\";s:6:\"Alumni\";s:9:\"seo_title\";s:6:\"Alumni\";s:8:\"seo_desc\";s:6:\"Alumni\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:3028:\"<div id=\"sloupec1\"><img src=\"\/images\/0!0\/uzel\/0136702\/0001~~K87JTEktUkjOTCrNyU5USM0DAA.png\" alt=\" \u25f3 slider cibulka en (png) \u2192 (origin\u00e1l)\" width=\"823\" height=\"200\"><br>\r\n<p><\/p>\r\n<table class=\"table_bezramecku\" style=\"height: 416px; float: left; width: 655px;\" width=\"525\">\r\n<tbody>\r\n<tr>\r\n<td style=\"width: 312.714px;\" scope=\"col\">\r\n<ul>\r\n<li>Tereza Bou\u0161kov\u00e1 (2026)<\/li>\r\n<li>Ivana Weisheitelov\u00e1 (Ph.D., 2025)<\/li>\r\n<li>Zuzana Abdelfattah (2025)<\/li>\r\n<li>Marie Rozmu\u0161ov\u00e1 (2025)<\/li>\r\n<li>Jan \u0158eh\u00e1\u010dek (2025)<\/li>\r\n<li>Jakub Semeck\u00fd (2024)<\/li>\r\n<li>R\u00f3bert Obert\u00edk (Ph.D., 2024)<\/li>\r\n<li>Amal Hassan Tolba (Ph.D., 2024)<\/li>\r\n<li>Petra M\u00edkov\u00e1 (2022)<\/li>\r\n<li>Ekaterina Zubova (2022)<\/li>\r\n<li>Anna Ml\u010dochov\u00e1 (2021)<\/li>\r\n<li>Krist\u00fdna Nademlejnsk\u00e1 (2021)<\/li>\r\n<li>Ivana Weisheitelov\u00e1 (2021)<\/li>\r\n<li>Lucie Wohlr\u00e1bov\u00e1 (2021)<\/li>\r\n<li>Jakub Copko (2020)<\/li>\r\n<li>Michal M\u00e4rz (Ph.D., 2020)<\/li>\r\n<li>Tom\u00e1\u0161 Hartman (Ph.D., 2019)<\/li>\r\n<li>Krist\u00fdna Jank\u016f (2018)<\/li>\r\n<li>Tom\u00e1\u0161 Nevesel\u00fd (2018)<\/li>\r\n<li>Adam Pokluda (2018)<\/li>\r\n<li>Jessica \u0160pa\u010dkov\u00e1 (2018)<\/li>\r\n<li>Leo\u0161 Valenta (2018)<\/li>\r\n<li>Viktor Mojr (Ph.D., 2017)<\/li>\r\n<li>Martin Cigl (Ph.D., 2017)<\/li>\r\n<li>Peter H\u00e1jek (2016)<\/li>\r\n<li>Michal Jir\u00e1sek (2016)<\/li>\r\n<li>Karol\u00edna Strakov\u00e1 (2016)<\/li>\r\n<li>Ji\u0159\u00ed \u0160turala (Ph.D., 2016)<\/li>\r\n<li>Hana Kotou\u010dov\u00e1 (Ph.D., 2015)<\/li>\r\n<li>David Just (2015)<\/li>\r\n<li>Jan Zelenka (2015)<\/li>\r\n<li>V\u00edt Zvon\u00ed\u010dek (2015)<\/li>\r\n<li>Tom\u00e1\u0161 Hartman (2014)<\/li>\r\n<li>Ond\u0159ej Koll\u00e1r (2014)<\/li>\r\n<li>Martin Kos (2014)<\/li>\r\n<li>Michal M\u00e4rz (2014)<\/li>\r\n<li>Petra Tomanov\u00e1 (2014)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<td style=\"width: 300.762px;\" scope=\"col\">\r\n<ul>\r\n<li>Radek Jurok (Ph.D., 2013)<\/li>\r\n<li>So\u0148a Boh\u00e1\u010dov\u00e1 (2013)<\/li>\r\n<li>Mat\u011bj Kala (2013)<\/li>\r\n<li>Kl\u00e1ra Ma\u0148\u00e1skov\u00e1 (2013)<\/li>\r\n<li>Ji\u0159\u00ed Mik\u0161\u00e1tko (2012)<\/li>\r\n<li>Jitka Da\u010fov\u00e1 (2011)<\/li>\r\n<li>Eva Kone\u010dkov\u00e1 (2011)<\/li>\r\n<li>Ji\u0159\u00ed \u0160turala (2011)<\/li>\r\n<li>Martin Cigl (2010)<\/li>\r\n<li>V\u00e1clav Eigner (2010)<\/li>\r\n<li>Petr Kova\u0159\u00ed\u010dek (2010)<\/li>\r\n<li>Petra M\u00e9nov\u00e1 (2010)<\/li>\r\n<li>Viktor Mojr (2010)<\/li>\r\n<li>Marta Sl\u00e1dkov\u00e1 (2008)<\/li>\r\n<li>Franti\u0161ek Kafka (2008)<\/li>\r\n<li>Michal \u0160\u00e1mal (2008)<\/li>\r\n<li>Lenka Baxov\u00e1 (2007)<\/li>\r\n<li>Radek Jurok (2007)<\/li>\r\n<li>Eva Svobodov\u00e1 (Ph.D., 2006)<\/li>\r\n<li>Jan P\u00edcha (Ph.D., 2006)<\/li>\r\n<li>Filip Kielar (2004)<\/li>\r\n<li>Martin K\u0159ov\u00e1\u010dek (2004)<\/li>\r\n<li>Michala Koz\u00e1kov\u00e1 (2003)<\/li>\r\n<li>Milan Kivala (2003)<\/li>\r\n<li>Robert R\u00f6dling (2003)<\/li>\r\n<li>Kate\u0159ina Sl\u00e1\u010dalov\u00e1 (Ph.D., 2003)<\/li>\r\n<li>Radek Cibulka (Ph.D., 2002)<\/li>\r\n<li>Eva Svobodov\u00e1 (Han\u00e1\u010dkov\u00e1) (2001)<\/li>\r\n<li>Kamil Ku\u010da (2001)<\/li>\r\n<li>Ond\u0159ej P\u00e1v (2001)<\/li>\r\n<li>Jan \u0160midrkal (1999)<\/li>\r\n<li>Tom\u00e1\u0161 Martin\u016f (1998)<\/li>\r\n<li>Hana Kotou\u010dov\u00e1 (1997)<\/li>\r\n<li>\u0160\u00e1rka Petrl\u00edkov\u00e1 (1997)<\/li>\r\n<li>Radek Cibulka (1996)<\/li>\r\n<li>Sonja Vo\u0161tov\u00e1 (1995)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><\/p>\r\n<p><\/p>\r\n<\/div>\r\n<div><\/div>\r\n<div id=\"sloupec2\">\r\n<p><\/p>\r\n<\/div>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["136703"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"136703":{"idvazba":"175436","nad_uzel":"142446","pod_uzel":"136703","url":"","sablona":"11","nazev":"Galerie absolventi","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"20.07.2026 15:36:00","platne_do":null,"iduzel":"136703","obsah":"a:4:{s:6:\"nadpis\";s:0:\"\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"121046":{"idvazba":"168101","nad_uzel":"116995","pod_uzel":"121046","url":"\/research\/cibulka-old","sablona":"49","nazev":"Cibulka","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old}","poradi":"4","skupina_www":"everyone","platne_od":"13.05.2026 07:56:00","platne_do":null,"iduzel":"121046","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:7:\"Cibulka\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:26:\"0001~~8_R1jzc2sDDXNQYA.jpg\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["122049","135607","121080","121050","121051","121058","136576"],"poduzly_count":7,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":5,"122049":{"idvazba":"150068","nad_uzel":"121046","pod_uzel":"122049","url":"","sablona":"4","nazev":"vypis podrizenych","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"30.04.2026 10:22:00","platne_do":null,"iduzel":"122049","obsah":"a:7:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:6:\"zelena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:4:\"true\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:7:\"-sticky\";s:4:\"text\";s:0:\"\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"135607":{"idvazba":"166708","nad_uzel":"121046","pod_uzel":"135607","url":"","sablona":"47","nazev":"Cibulka research group (Hyde Park)","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"30.04.2026 10:20:00","platne_do":null,"iduzel":"135607","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121080":{"idvazba":"150035","nad_uzel":"121046","pod_uzel":"121080","url":"","sablona":"55","nazev":"Cibulka","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"02.02.2026 14:50:00","platne_do":null,"iduzel":"121080","obsah":"a:16:{s:7:\"skupina\";s:0:\"\";s:17:\"skupina_podnadpis\";s:0:\"\";s:10:\"titul_pred\";s:10:\"Prof. Ing.\";s:5:\"jmeno\";s:5:\"Radek\";s:8:\"prijmeni\";s:7:\"Cibulka\";s:8:\"titul_za\";s:5:\"Ph.D.\";s:10:\"department\";s:33:\"Head of Department \/ Group Leader\";s:7:\"obrazek\";s:31:\"0001~~C0pMSc1WcM5MKs3JTgQA.jpeg\";s:5:\"email\";s:22:\"radek.cibulka@vscht.cz\";s:13:\"telefon_pevna\";s:15:\"+420 22044 4182\";s:13:\"telefon_mobil\";s:0:\"\";s:9:\"idtelefon\";s:3:\"504\";s:11:\"text_odkazu\";s:27:\"A255 (Building A, Room 255)\";s:5:\"odkaz\";s:32:\"https:\/\/emil.vscht.cz\/maps\/27022\";s:5:\"obsah\";s:0:\"\";s:7:\"bg_gray\";s:1:\"0\";}","class":"contact","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121050":{"idvazba":"149011","nad_uzel":"121046","pod_uzel":"121050","url":"","sablona":"4","nazev":"Contacts","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"02.02.2026 16:37:00","platne_do":null,"iduzel":"121050","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121051":{"idvazba":"149057","nad_uzel":"121046","pod_uzel":"121051","url":"\/research\/cibulka-old\/people","sablona":"49","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/people}","poradi":"4","skupina_www":"everyone","platne_od":"02.02.2026 10:49:00","platne_do":null,"iduzel":"121051","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["121080","122018","121052","121053","39232","38649","121054","121054","121055","121056","121056"],"poduzly_count":11,"poduzly_count_aut":5,"poduzly":{"poduzly_count_aut_sum":0,"121080":{"idvazba":"150035","nad_uzel":"121046","pod_uzel":"121080","url":"","sablona":"55","nazev":"Cibulka","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"02.02.2026 14:50:00","platne_do":null,"iduzel":"121080","obsah":"a:16:{s:7:\"skupina\";s:0:\"\";s:17:\"skupina_podnadpis\";s:0:\"\";s:10:\"titul_pred\";s:10:\"Prof. Ing.\";s:5:\"jmeno\";s:5:\"Radek\";s:8:\"prijmeni\";s:7:\"Cibulka\";s:8:\"titul_za\";s:5:\"Ph.D.\";s:10:\"department\";s:33:\"Head of Department \/ Group Leader\";s:7:\"obrazek\";s:31:\"0001~~C0pMSc1WcM5MKs3JTgQA.jpeg\";s:5:\"email\";s:22:\"radek.cibulka@vscht.cz\";s:13:\"telefon_pevna\";s:15:\"+420 22044 4182\";s:13:\"telefon_mobil\";s:0:\"\";s:9:\"idtelefon\";s:3:\"504\";s:11:\"text_odkazu\";s:27:\"A255 (Building A, Room 255)\";s:5:\"odkaz\";s:32:\"https:\/\/emil.vscht.cz\/maps\/27022\";s:5:\"obsah\";s:0:\"\";s:7:\"bg_gray\";s:1:\"0\";}","class":"contact","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"122018":{"idvazba":"150034","nad_uzel":"121051","pod_uzel":"122018","url":"","sablona":"47","nazev":"Seznam lid\u00ed","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.02.2026 10:49:00","platne_do":null,"iduzel":"122018","obsah":"a:4:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:4:\"bila\";s:4:\"text\";s:3310:\"<h2>Employees:<\/h2>\r\n<ul>\r\n<li>Prof. Radek Cibulka&nbsp; &nbsp; &nbsp;&nbsp;<span class=\"cervena0\"><span class=\"cerna0\"><a href=\"people\/39224\" target=\"_blank\" class=\"jstree-anchor jstree-hovered\" rel=\"follow noopener\">(CV)<\/a><\/span><\/span><\/li>\r\n<li>Dr.&nbsp;Eva Svobodov\u00e1 <a href=\"people\/39226\" target=\"_blank\" rel=\"noopener\">(CV)<\/a><\/li>\r\n<li>Dr. Roman Holakovsk\u00fd&nbsp;<a href=\"http:\/\/uoch.vscht.cz\/vedecke-skupiny\/cibulka\/lide\/16610\" target=\"_blank\" rel=\"noopener\">(CV)<\/a><\/li>\r\n<li><span style=\"display: inline !important; float: none; background-color: #ffffff; color: #333333; font-family: 'source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; list-style-image: none; list-style-position: outside; list-style-type: none; orphans: 2; text-align: left; text-decoration: none; text-indent: -1.2em; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;\">Dr. Tetiana Pavlovska (post-doc)<\/span><\/li>\r\n<li><span style=\"display: inline !important; float: none; background-color: #ffffff; color: #333333; font-family: 'source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; list-style-image: none; list-style-position: outside; list-style-type: none; orphans: 2; text-align: left; text-decoration: none; text-indent: -1.2em; text-transform: none; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px;\">Dr. Dorian Dupommier (post-doc)<\/span><\/li>\r\n<li>Martina Kovandov\u00e1<\/li>\r\n<\/ul>\r\n<div class=\"spolupr\u00e1ce\">\r\n<h2>&nbsp;<\/h2>\r\n<h2>Ph.D. students:<\/h2>\r\n<ul>\r\n<li>Ing. Ekaterina Zubova<\/li>\r\n<li>Ing. Adam Pokluda<\/li>\r\n<li>Ing. Rostislav Sponar<\/li>\r\n<li>Ing. Jakub Semeck\u00fd<\/li>\r\n<li>Ing. Marie Rozmu\u0161ov\u00e1<\/li>\r\n<\/ul>\r\n<h2>&nbsp;<\/h2>\r\n<h2>Students:<\/h2>\r\n<p><\/p>\r\n<ul>\r\n<li>Tereza Bou\u0161kov\u00e1<\/li>\r\n<li>Viktor Vojan<\/li>\r\n<li>\u0160t\u011bp\u00e1n Slabina<\/li>\r\n<li>Krist\u00fdna \u0160oltov\u00e1<\/li>\r\n<li>Kate\u0159ina Riegerov\u00e1<\/li>\r\n<li>Barbora Z\u00edtkov\u00e1<\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<h2>&nbsp;<\/h2>\r\n<h2>Collaborations:<\/h2>\r\n<ul>\r\n<li>Prof. Marek Sikorski&nbsp;<\/li>\r\n<li>Prof. Ji\u0159\u00ed Ludv\u00edk&nbsp;<\/li>\r\n<li>Prof. Burkhard K\u00f6nig<\/li>\r\n<li>Dr. Ullrich Jahn<\/li>\r\n<li>Dr. Tom\u00e1\u0161 Slanina<\/li>\r\n<\/ul>\r\n<\/div>\r\n<div class=\"host\u00e9\">\r\n<h2>&nbsp;<\/h2>\r\n<h2>Guests:<\/h2>\r\n<ul>\r\n<li>Marina Oka (Japan, 2024)<\/li>\r\n<li>Sven St\u00f6ver (Germany, 2023)<\/li>\r\n<li>Ester Sans Panades (Spain, 2021)<\/li>\r\n<li>Vincent George (Germany, 2019)<\/li>\r\n<li>Dharmik Gadhiya (Polsko, 2019)<\/li>\r\n<li>Killiann Heinz (Francie, 2019, 2020)<\/li>\r\n<li>Tribout Camille (Francie, 2018)<\/li>\r\n<li>Thibaud Bailly (France, 2018)<\/li>\r\n<li>Jehanne Grimmer (France, 2017)<\/li>\r\n<li>Sarah Bailly (France, 2017)<\/li>\r\n<li>Guillaume Hoffmann (France, 2016)<\/li>\r\n<li>Dr. Dorota Prukala (Poland, 2014, 2015)<\/li>\r\n<li>Nadia Ryter (Switzerland, 2010)<\/li>\r\n<li>Smita Gunnoo (UK, 2008)<\/li>\r\n<li>Andreja \u010condor (Croatia, 2007)<\/li>\r\n<li>Serkan Sayin (Turkey, 2007)<\/li>\r\n<li>Jenna Scotcher (UK, 2006)<\/li>\r\n<li>Baptiste Plancq (France, 2005)<\/li>\r\n<li>Markus W. Kriegl (Austria, 2005)<\/li>\r\n<li>Tilman Schulz (Germany, 2004)<\/li>\r\n<li>Yuliya Milaslavina (Belarus, 2002)<\/li>\r\n<li>Rina Matsumi (Japan, 2001)<\/li>\r\n<\/ul>\r\n<\/div>\";s:7:\"bg_gray\";s:1:\"0\";}","class":"infotext","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121052":{"idvazba":"149013","nad_uzel":"121051","pod_uzel":"121052","url":"","sablona":"11","nazev":"Employees","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"29.01.2026 17:01:54.444729","platne_do":null,"iduzel":"121052","obsah":"a:1:{s:6:\"nadpis\";s:9:\"Employees\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121053":{"idvazba":"149014","nad_uzel":"121051","pod_uzel":"121053","url":"","sablona":"11","nazev":"Ph.D. Students","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"29.01.2026 17:01:54.544525","platne_do":null,"iduzel":"121053","obsah":"a:4:{s:6:\"nadpis\";s:14:\"Ph.D. Students\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"39232":{"idvazba":"149015","nad_uzel":"121051","pod_uzel":"39232","url":"","sablona":"20","nazev":"Slider Cibulka - en","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"25.05.2017 15:31:40.176327","platne_do":null,"iduzel":"39232","obsah":null,"class":"slider","autonomni":"0","pod_uzly":["39233","53750","95160","95161"],"poduzly_count":4,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"39233":{"idvazba":"41710","nad_uzel":"39232","pod_uzel":"39233","url":"","sablona":"20","nazev":"slider-en","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"39233","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:36:\"0001~~K87JTEktUkjOTCrNyU5USM0DAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"53750":{"idvazba":"62162","nad_uzel":"39232","pod_uzel":"53750","url":"","sablona":"20","nazev":"lide - en","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"53750","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:56:\"0001~~K87JTEktUnDOTCrNyU5USMsvyVcozi4tyMyrVDAyMDIFAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"95160":{"idvazba":"118048","nad_uzel":"39232","pod_uzel":"95160","url":"","sablona":"20","nazev":"fotochemie - en","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"95160","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:33:\"0001~~K87JTEktUiirrMouzVUwBAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"95161":{"idvazba":"118049","nad_uzel":"39232","pod_uzel":"95161","url":"","sablona":"20","nazev":"laborato\u0159 - en","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"95161","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:33:\"0001~~K87JTEktUiirrMouzVUwAgA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"38649":{"idvazba":"149016","nad_uzel":"121051","pod_uzel":"38649","url":"","sablona":"4","nazev":"Cibulka's Group","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"30.01.2026 09:51:00","platne_do":null,"iduzel":"38649","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"121054":{"idvazba":"149017","nad_uzel":"121051","pod_uzel":"121054","url":"\/research\/cibulka-old\/people\/121054","sablona":"49","nazev":"Prof. Ing. Radek Cibulka","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/people\/121054}","poradi":"7","skupina_www":"everyone","platne_od":null,"platne_do":null,"iduzel":"121054","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:24:\"Prof. Ing. Radek Cibulka\";s:8:\"seo_desc\";s:24:\"Prof. Ing. Radek Cibulka\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:27740:\"<p><img src=\"\/images\/0!0\/uzel\/0039224\/0001~~C0pMSc1WcM5MKs3JTgQA.png\" class=\"img_float_right img_fancy_no\" alt=\" \u25f3 Radek Cibulka (png) \u2192 (origin\u00e1l)\" width=\"220\" height=\"249\"><\/p>\r\n<h2 style=\"text-align: center;\">Curriculum Vitae<\/h2>\r\n<h2 style=\"text-align: center;\"><strong><span class=\"modra0\">Prof. Radek Cibulka, Ph.D.<\/span><\/strong><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"modra0\">(ID: H-1298-2016, ORCID ID: 0000-0002-8584-7715)<\/span><\/p>\r\n<p style=\"text-align: left;\">&nbsp;<\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"><\/span><\/b><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"><\/span><\/b><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">Career summary:<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; tab-stops: list 35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">1996<\/span><\/i><b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">M.Sc. University of Chemistry and Technology, Prague (UCT Prague), Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; tab-stops: list 35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2002<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span> <\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">Ph.D. with F. Li\u0161ka, Department of Organic Chemistry, UCT Prague, Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; tab-stops: list 35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2003<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">post-doc with B. K\u00f6nig, Department of Organic Chemistry, University of Regensburg, Germany<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -32.45pt; mso-char-indent-count: -2.95; margin: 0cm 0cm 0cm 32.45pt;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2004<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp; <\/span><\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">Assistant professor, Department of Organic Chemistry, UCT Prague, Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -32.45pt; mso-char-indent-count: -2.95; margin: 0cm 0cm 0cm 32.45pt;\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2009<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp; <\/span>Associate Professor, Department of Organic Chemistry, UCT Prague, Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -32.45pt; mso-char-indent-count: -2.95; margin: 0cm 0cm 8.0pt 32.45pt;\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">since 2017<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\"> Full professor, Department of Organic Chemistry, UCT Prague, Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 8.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\">Research interests<\/span><\/b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB; mso-bidi-font-weight: bold;\">;<\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"> Photoredox catalysis;<span style=\"mso-bidi-font-weight: bold;\"> Catalysis in redox reactions;<\/span> Flavin-based redox and photoactive systems;<span style=\"mso-bidi-font-weight: bold;\"> Biomimetic reactions; Heterocyclic chemistry; Electrocatalysis; Flavoenzymes<o:p><\/o:p><\/span><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\">Selected projects<\/span><\/b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"> since 2020: <o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">2019 \u2013 2021<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">Organic<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">photoredox<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">catalysis<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">in<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">reductive<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">transformations:<\/span><span lang=\"EN-GB\" style=\"font-size: 4.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">new<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">area<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">for<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">flavin<\/span><span lang=\"EN-GB\" style=\"font-size: 8.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 14.0pt; mso-ansi-language: EN-GB;\">derivatives<\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"Default\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\">2021 \u2013 2023<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-bidi-font-style: italic;\">Novel umpolung strategy using flavin covalent organocatalysis <o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"Default\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\">2021 \u2013 2023<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-bidi-font-style: italic;\">Tailoring flavins for organic photocatalysis <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"Default\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\">2023 \u2013 2025<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span lang=\"EN-US\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-US;\">Merging photochemistry and electrochemistry in flavin-based redox catalysis<\/span><span lang=\"EN-US\" style=\"font-size: 10.0pt; mso-bidi-font-size: 14.0pt; mso-bidi-font-style: italic;\"> <\/span><span style=\"font-size: 10.0pt; mso-bidi-font-size: 14.0pt; mso-bidi-font-style: italic;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 8.0pt;\" class=\"Default\"><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\">2024 \u2013 2026<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span lang=\"EN-US\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-US;\">Photoredox catalysis with organic anions \u2013 perspective area for flavin derivatives<\/span><span lang=\"EN-US\" style=\"font-size: 10.0pt; mso-bidi-font-size: 14.0pt; mso-bidi-font-style: italic;\"> <\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">Education:<\/span><\/b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\"> <o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 8.0pt;\" class=\"MsoNormal\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">Lectures in Retrosynthesis (2011-now); Organic chemistry (2011-now); courses in Laboratory of organic chemistry (2011 \u2013 2015); co-author of internet portal for education of organic chemistry (2011 \u2013 2012); Supervisor of 13 Ph.D. thesis (8 finished, 5 ongoing), 26 diploma thesis and 25 bachelor thesis (finished).<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 2.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">Selected papers in catalysis and photoredox catalysis since 2020:<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify; text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoNormal\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><b style=\"mso-bidi-font-weight: normal;\"><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt;\">Cibulka R.<\/span><\/b><sup><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt;\">*<\/span><\/sup><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt;\">: Strong chemical reducing agents produced by light <span class=\"emphasis\"><i><span style=\"color: #222222;\">Nature<\/span><\/i><\/span><span style=\"color: #222222; background: white;\"> <b style=\"mso-bidi-font-weight: normal;\">2020<\/b>, <\/span><strong><i style=\"mso-bidi-font-style: normal;\"><span style=\"color: #222222; font-weight: normal; mso-bidi-font-weight: bold;\">580<\/span><\/i><\/strong><span style=\"color: #222222;\">, 31-32.<\/span><\/span><span style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-ansi-language: CS;\">Graml A., Nevesel\u00fd T., Kutta R.-J.*, <b style=\"mso-bidi-font-weight: normal;\">Cibulka R.<\/b>*, K\u00f6nig B.*: Deazaflavin reductive photocatalysis involves excited semiquinone radicals <i style=\"mso-bidi-font-style: normal;\">Nat. Commun.<\/i> <b style=\"mso-bidi-font-weight: normal;\">2020<\/b>, <i style=\"mso-bidi-font-style: normal;\">11<\/i>, 3174.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-ansi-language: CS;\">Tolba A. H., Krupi\u010dka M., Chudoba J., <b style=\"mso-bidi-font-weight: normal;\">Cibulka R.*<\/b>: Amide bond formation via aerobic photooxidative coupling of alde-hydes with amines catalyzed by a riboflavin derivative <i style=\"mso-bidi-font-style: normal;\">Org. Lett.<\/i> <b style=\"mso-bidi-font-weight: normal;\">2021<\/b>, <i style=\"mso-bidi-font-style: normal;\">23<\/i>, 6825.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-ansi-language: CS;\">Pavlovska T., Kr\u00e1l Lesn\u00fd D., Svobodov\u00e1 E., Hoskovcov\u00e1 I., Archipowa N., Kutta R. J.*, <b style=\"mso-bidi-font-weight: normal;\">Cibulka R.<\/b>*: Tuning Deazaflavins Towards Highly Potent Reducing Photocatalysts Guided by Mechanistic Understanding - Enhancement of the Key Step by the Internal Heavy Atom Effect. <i style=\"mso-bidi-font-style: normal;\">Chem. Eur. J.<\/i> <b style=\"mso-bidi-font-weight: normal;\">2022<\/b>, <i style=\"mso-bidi-font-style: normal;\">28<\/i>, e20220076. <b style=\"mso-bidi-font-weight: normal;\">Hot Paper<\/b>.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 10.0pt; mso-bidi-font-size: 11.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\">Obert\u00edk R., Chudoba J., \u0160turala J., Tar\u00e1bek J., Ludv\u00edkov\u00e1 L., Slanina T., K\u00f6nig B., <b style=\"mso-bidi-font-weight: normal;\">Cibulka R.<\/b>*: Highly Chemoselective Catalytic Photooxidations by Using Solvent as a Sacrificial Electron Acceptor <\/span><i style=\"mso-bidi-font-style: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt;\">Chem. Eur. J. <\/span><\/i><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt;\">2022<\/span><\/b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt;\">, <i style=\"mso-bidi-font-style: normal;\">28<\/i>, e202202487.<b style=\"mso-bidi-font-weight: normal;\"> VIP<\/b><i style=\"mso-bidi-font-style: normal;\">.<\/i><\/span><span style=\"font-size: 10.0pt; mso-bidi-font-size: 11.0pt; mso-ansi-language: CS;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\">Pavlovska T., Weisheitelov\u00e1 I., Pramthaisong C., Sikorski M., Jahn U., <b>Cibulka R.<\/b>*: Primary and Secondary Amines by Flavin\u2010Photocatalyzed Consecutive Desulfonylation and Dealkylation of Sulfonamides. <i>Adv. Synth. Catal.<\/i> <b>2023<\/b>, <i>365<\/i>, 4662.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\">Venkatraman R. K., Hassan Tolba A., Solling T., <b>Cibulka R.<\/b>, El-Zohry A.*: Ultrafast Events of Photoexcited Iron(III)chloride for Activation of Benzylic C\u2013H Bonds. <i>J. Phys. Chem. Lett.<\/i> <b>2024<\/b>, <i>15<\/i>, 6202.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\">Weisheitelov\u00e1 I., Varma N., Chudoba J., Burdzi\u0144ski G., Sikorski M., <b>Cibulka R.<\/b>*: Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled by DMSO solvent. <i>Green Chem.<\/i> <b>2024<\/b>, <i>26<\/i>, 4880.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-indent: -14.2pt; mso-list: l0 level1 lfo1; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><!-- [if !supportLists]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol; mso-ansi-language: CS;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\">Pavlovska T., Havl\u00edk M., Lab\u00edkov\u00e1 M., <b>Cibulka R.*<\/b>: Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids andOligopeptides via Flavin N(5)-iminium Covalent Adducts. <i>Adv. Synth. Catal. <\/i><b>2025<\/b>, accepted. DOI: 10.1002\/adsc.202401556<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoBodyText\"><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt; mso-ansi-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 3.0pt;\" class=\"MsoNormal\"><b style=\"mso-bidi-font-weight: normal;\"><span lang=\"EN-GB\" style=\"font-size: 11.0pt; mso-bidi-font-size: 10.0pt; mso-ansi-language: EN-GB;\">Book Editor:<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"text-align: justify; text-indent: -14.2pt; mso-list: l1 level1 lfo2; margin: 0cm 0cm 3.0pt 14.2pt;\" class=\"MsoNormal\"><!-- [if !supportLists]--><span style=\"font-size: 8.0pt; mso-bidi-font-size: 10.0pt; font-family: Symbol; mso-fareast-font-family: Symbol; mso-bidi-font-family: Symbol;\"><span style=\"mso-list: Ignore;\">-<span style=\"font: 7.0pt 'Times New Roman';\">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/span><!--[endif]--><b style=\"mso-bidi-font-weight: normal;\"><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt;\">Cibulka R.<\/span><\/b><span style=\"font-size: 11.0pt; mso-bidi-font-size: 12.0pt;\">, Fraaije M. W., Eds.: Flavin-Based Catalysis, Principles and Application, Wiley-VCH Verlag GmbH, <b style=\"mso-bidi-font-weight: normal;\">2021<\/b>; Print ISBN:9783527348343; Online ISBN:9783527830138; DOI:10.1002\/9783527830138 + 3 chapters in this book.<\/span><span style=\"font-size: 8.0pt; mso-bidi-font-size: 10.0pt;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 3.0pt; text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 8.0pt; mso-bidi-font-size: 10.0pt;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; margin: 0cm 0cm 2.0pt 0cm;\"><b><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">Awards:<o:p><\/o:p><\/span><\/b><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">1996<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">Prize of Josef Hlavka from Hlavka\u2019s Foundation<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2002<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">Unipetrol Prize from Unipetrol and University of Chemistry and Technology, Prague<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2004<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span>Young Chemistry Award in Organic Chemistry from Sigma-Aldrich in the Czech Republic<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2005<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span>Alfred Bader Prize for Organic Chemistry from the Czech Chemical Society<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2010<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span>Karel Preis Prize for the best article in Chemick\u00e9 listy from the Czech Chemical Society<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB;\">2022<\/span><\/i><span lang=\"EN-GB\" style=\"font-size: 11.0pt; font-family: 'Times New Roman',serif; mso-ansi-language: EN-GB; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif; mso-bidi-font-style: italic;\">Chemistry Europe Fellow<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin: 0cm; text-align: justify;\"><i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif;\">2022<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif; mso-bidi-font-style: italic;\">Milo\u0161 Hudlick\u00fd Prize for the best work published by Czech authors in European journals<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif;\">2022<\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif; mso-bidi-font-style: italic;\"><span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span>Rudolf Luke\u0161 Prize awarded from the Czech Chemical Society and Experientia for excellent results in the field of organic chemistry<i><o:p><\/o:p><\/i><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; margin: 0cm 0cm 0cm 35.45pt;\"><i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif;\">2023<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif; mso-bidi-font-style: italic;\">Honorary recognition of the chairman of the GA CR for the project \u201eOrganic photoredox catalysis in reductive transformations: new area for flavin derivatives\u201c<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify; text-indent: -35.45pt; margin: 0cm 0cm 8.0pt 35.45pt;\"><i style=\"mso-bidi-font-style: normal;\"><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif;\">2023<span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span><\/span><\/i><span style=\"font-size: 11.0pt; mso-bidi-font-size: 8.5pt; font-family: 'Times New Roman',serif; mso-bidi-font-style: italic;\">Award of the Minister of Education, Youth and Sports for excellent educational activities at university<o:p><\/o:p><\/span><\/p>\r\n<p>&nbsp;In Prague, April 2025<\/p>\r\n<h2><strong><em>&nbsp;<\/em><\/strong><\/h2>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"121055":{"idvazba":"149018","nad_uzel":"121051","pod_uzel":"121055","url":"\/research\/cibulka-old\/people\/121055","sablona":"1","nazev":"Roman Holakovsk\u00fd - en","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/people\/121055}","poradi":"8","skupina_www":"everyone","platne_od":null,"platne_do":null,"iduzel":"121055","obsah":"s:0:\"\";","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"121056":{"idvazba":"149019","nad_uzel":"121051","pod_uzel":"121056","url":"\/research\/cibulka-old\/people\/121056","sablona":"49","nazev":"Dr. Eva Svobodov\u00e1","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/people\/121056}","poradi":"10","skupina_www":"everyone","platne_od":"29.01.2026 17:01:54.737854","platne_do":null,"iduzel":"121056","obsah":"a:9:{s:5:\"nazev\";s:18:\"Dr. Eva Svobodov\u00e1\";s:9:\"seo_title\";s:18:\"Dr. Eva Svobodov\u00e1\";s:8:\"seo_desc\";s:18:\"Dr. Eva Svobodov\u00e1\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:2583:\"<h2><strong><em><img src=\"\/images\/0!215\/uzel\/0039226\/0001~~cy1LVAguy0_KT8kvSwQA.jpg\" class=\"img_float_right img_fancy_no\" alt=\"Eva Svobodova (v\u00fd\u0161ka 215px)\" width=\"161\" height=\"215\"><\/em><\/strong><\/h2>\r\n<h2 style=\"text-align: center;\">Curriculum Vitae<\/h2>\r\n<h2 style=\"text-align: center;\"><strong><span class=\"modra0\">Ing. Eva Svobodov\u00e1, Ph.D.<\/span><\/strong><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"modra0\">(ID: AAE-5727-2021, ORCID ID: 0000-0002-4809-2659)<\/span><\/p>\r\n<h2><strong><em>&nbsp;<\/em><\/strong><\/h2>\r\n<p><strong>&nbsp;<\/strong><strong>Personal data:<\/strong><\/p>\r\n<p>Name:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ing. Eva Svobodov\u00e1, Ph.D.<br>Born:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 18.1.1978 in Vset\u00edn, Czech Republic<br>Marital status:&nbsp;&nbsp;&nbsp;&nbsp; married, 2 children (born in 2008 and 2010)<br>e-mail:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <a href=\"mailto:svobodoe@vscht.cz\">svobodoe@vscht.cz<\/a><\/p>\r\n<p><strong>Career Summary:<\/strong><\/p>\r\n<p>1992-1996&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Grammar school in Vset\u00edn, Czech Republic<br>1996-2001&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; M.Sc. with F. Li\u0161ka, University of Chemistry and Technology, Prague, Czech Republic<br>2001-2006&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ph.D. with F. Hampl, University of Chemistry and Technology, Prague, Czech Republic<br>Since 2006&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Assistant professor, Department of Organic Chemistry, University of Chemistry and Technology, Prague. Czech&nbsp; Republic<\/p>\r\n<p><strong>Awards:<\/strong><\/p>\r\n<p>The Foundation CURIE BRATISLAVA SIS\u00b403 Award - the best student presentation on 10<sup>th<\/sup> International conference Separation of Ionic Solutes, Podbansk\u00e9, Vysok\u00e9 Tatry, Slovakia, 6 \u2013 11. 9. 2003.<\/p>\r\n<p><strong>Teaching Activity:<\/strong><\/p>\r\n<p>Lectures in Organic chemistry, courses in Laboratory of organic chemistry.<br>Supervising of bachelor and magister thesis.<\/p>\r\n<p><strong>Research Interest:<br><\/strong><\/p>\r\n<p>Chemistry of heterocyclic compounds, flavins and their derivatives, photocatalysis<\/p>\r\n<p><strong>&nbsp;Publication Activity:<\/strong><\/p>\r\n<p>17 original papers in impacted journals, 1 patent, 31 presentations on conferences (author or co-author)<br>H-index: 12<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"121058":{"idvazba":"149023","nad_uzel":"121046","pod_uzel":"121058","url":"\/research\/cibulka-old\/publications","sablona":"49","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/publications}","poradi":"5","skupina_www":"everyone","platne_od":"30.01.2026 08:52:00","platne_do":null,"iduzel":"121058","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:77623:\"<h3>2026<\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Sponar R., Li\u0161ka A., Cibulka R.: Electrochemistry Facilitates the hemoselectivity of Benzylic Alcohol Oxidations Mediated by Flavin-Based Photoredox Catalysis, <i>Org. Lett. <\/i><b>2026<\/b>, <i>accepted<\/i>. <a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.5c04603\" target=\"_blank\" rel=\"noopener\">DOI:10.1021\/acs.orglett.5c04603<\/a>.<\/span><\/p>\r\n<h3>2025<\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt; line-height: 107%;\">Weisheitelov\u00e1 I., Varma N., \u0160imkov\u00e1 L., Chudoba J., Pavlovska T., Gulaczyk I., Burdzi\u0144ski G., Ludv\u00edk J., Sikorski M., Cibulka R.: Deazaalloxazines \u2013 Flavin Derivatives That Provide Reductive Photoredox Catalysis with Inert Substrates, <i>Chem. Eur. J.<\/i> <b>2025<\/b>, e02897, <i>accepted<\/i>. <a href=\"https:\/\/doi.org\/10.1002\/chem.202502897\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.202502897<\/a>.<\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">\u0160imkov\u00e1 L., Svobodov\u00e1 E., Li\u0161ka A., Lu\u0161pai K., Cibulka R., Ludv\u00edk J.: Redox properties of flavin derivatives: A Comparative study, <i>Electrochim. Acta<\/i> <b>2025<\/b>, <i>accepted<\/i>, <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2025.147520\">DOI:10.1016\/j.electacta.2025.147520<\/a><\/span><o:p><\/o:p><\/p>\r\n<table border=\"1\" style=\"border-collapse: collapse; width: 99.9691%;\"><colgroup><col style=\"width: 79.6599%;\"><col style=\"width: 20.3091%;\"><\/colgroup>\r\n<tbody>\r\n<tr>\r\n<td><span style=\"font-size: 12.0pt;\">Tolba A. H., El-Zohry A., Khan J. I., Svobodov\u00e1 E. Chudoba J., Kl\u00edma J., Lu\u0161pai K. Pi\u017el M., \u0160turala J., Cibulka R.: Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations <i>Nat. Commun.&nbsp;<\/i><b>2025<\/b>, <i>16<\/i>, 7851. <span class=\"identifier doi\" style=\"font-size: 15px;\"><a href=\"https:\/\/doi.org\/10.1038\/s41467-025-63233-4\" target=\"_blank\" rel=\"noopener\" data-ga-category=\"full_text\" data-ga-action=\"DOI\">DOI:10.1038\/s41467-025-63233-4<\/a><\/span><\/span><\/td>\r\n<td><span style=\"font-size: 12.0pt;\"><img src=\"\/images\/0!0\/uzel\/0007830\/0005~~MwEA.png\" class=\"img_float_right\" alt=\" \u25f3 4 (png) \u2192 (origin\u00e1l)\" width=\"100\" height=\"100\"><\/span><\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p class=\"MsoNormal\"><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">R\u00fcckel J., Pavlovska T., Gawrona M., Cibulka R., Wolf R.: Deazaflavin-Catalyzed Arylation of White Phosphorus with Aryl Bromides and Chlorides, <i>Adv. Synth. Catal.<\/i> <b>2025<\/b>, 367, e70005.&nbsp; <a href=\"https:\/\/doi.org\/10.1002\/adsc.202500435\" target=\"_blank\" rel=\"noopener\"><\/a><a href=\"https:\/\/doi.org\/10.1002\/adsc.70005\">DOI:10.1002\/adsc.70005<\/a><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Pruka\u0142a D., Zubova E., Svobodov\u00e1 E., \u0160imkov\u00e1 L., Varma N., Chudoba J., Ludv\u00edk J., Burdzinski G., Gulaczyk G., Sikorski M., Cibulka R.: Introduction of flavin anions into photoredox catalysis: Acid-base equilibria of lumichrome allows photoreductions with an anion of an elusive 10-unsubstituted isoalloxazine,&nbsp;<i>Chem. Sci. <\/i><b>2025<\/b>, <em>16<\/em>, 11255-11263.&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D5SC01630D\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC01630D<\/a><br><strong>Cover picture<\/strong>: <em>Chem. Sci.<\/em>, 2025, 16, 11681. <a href=\"https:\/\/doi.org\/10.1039\/D5SC90144H\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC90144H<\/a><\/span><\/p>\r\n<p class=\"MsoNormal\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Bure\u0161ov\u00e1<\/span> Z.,<\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt;\">&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">Grygarov\u00e1<\/span> M., Prokopov\u00e1<\/span><span class=\"react-xocs-alternative-link\"> E., Klikar<\/span> M., Pytela O.<span style=\"font-size: 12.0pt; color: #1f1f1f;\">,&nbsp;<\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">V\u00e1\u0148a J.,<span style=\"color: #1f1f1f;\">&nbsp;<\/span>Fahim M. A. M.,<span style=\"color: #1f1f1f;\">&nbsp;<\/span><\/span><\/span><span class=\"given-name\"><span style=\"font-size: 12.0pt;\">Kanyashree<\/span><\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt;\">&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">J.<\/span><\/span><span class=\"react-xocs-alternative-link\"><span style=\"font-size: 12.0pt; color: #1f1f1f;\">,&nbsp;<\/span><\/span><span class=\"text\"><span style=\"font-size: 12.0pt;\">Zubova E.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Bart\u00e1\u010dek J.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Tydlit\u00e1t J., R\u016f\u017ei\u010dkov\u00e1 Z.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Cibulka R., Schanze K. S.<span style=\"color: #1f1f1f;\">,&nbsp;<\/span>Bure\u0161 F.: Divergent photoreduction of nitroaromatic compounds catalysed by dithienoquinoxaline, <i>J. Catal. <\/i><b>2025<\/b>, <em>445<\/em>, 116033. <a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2025.116033\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2025.116033<\/a><o:p><\/o:p><\/span><\/span>&nbsp;<span style=\"font-size: 12.0pt;\"> <\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><br><\/span><span style=\"font-size: 12.0pt;\">Pavlovska T., Havl\u00edk M., Lab\u00edkov\u00e1 M., Cibulka R.: Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids andOligopeptides via Flavin N(5)-iminium Covalent Adducts.&nbsp;<i>Adv. Synth. Catal.<\/i> <b>2025<\/b>, <em>367<\/em>,&nbsp; e202401556. <a href=\"https:\/\/doi.org\/10.1002\/adsc.202401556\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.202401556<\/a>&nbsp;<br><strong><span style=\"font-size: 12.0pt; line-height: 107%; font-family: source_sans_proregular; color: #464646; background: white;\">recognized by Synfacts (<\/span><span style=\"font-family: 'Segoe UI',sans-serif;\">H. Yamamoto and T. Hattori: Synfacts 2025 Vol. 21 Issue 05 Pages 543-543, <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2558-1150\" target=\"_blank\" rel=\"noopener\">DOI: 10.1055\/a-2558-1150<\/a>)<\/span><\/strong><br><\/span><o:p><\/o:p><span style=\"font-size: 12.0pt;\"><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Obert\u00edk R., Ludv\u00edkov\u00e1 L., Chudoba J., Cibulka R.: Chemoselective Anaerobic Dehydrogenation of Alcohols By Using Visible Light and a Positively Charged Deazaflavin Catalyst Regenerated by Acetonitrile Solvent. <i>ChemCatChem<\/i>&nbsp;<strong><span class=\"pubYear\">2025<\/span><\/strong><span>,&nbsp;<\/span><span class=\"vol\">17<\/span><span>, e202401795<\/span>.&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/cctc.202401795\">DOI:10.1002\/cctc.202401795<\/a><\/span><\/span><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><\/span><\/span><\/p>\r\n<h3>2024<span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><\/span><\/span><\/h3>\r\n<p><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Nizi\u0144ski S., Varma N., Sikorski M., Tobrman T., Svobodov\u00e1 E., Cibulka R., Rode M. F., Burdzinski G.: Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivative.&nbsp;<i>Sci Rep<\/i> <b>2024<\/b>, <i>14<\/i>, 24375. <a href=\"https:\/\/doi.org\/10.1038\/s41598-024-75239-x\">DOI:10.1038\/s41598-024-75239-x<\/a>.<\/span><\/span><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Weisheitelov\u00e1 I., Cibulka R., Sikorski M., Pavlovska T.: A facile three-component route to powerful 5-aryldeazaalloxazine photocatalysts.&nbsp;<i>Beilstein J. Org. Chem.<\/i> <b>2024<\/b>, <i>20<\/i>, 1831\u20131838.&nbsp; <a href=\"https:\/\/doi.org\/10.3762\/bjoc.20.161\">DOI:10.3762\/bjoc.20.161<\/a><\/span><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Venkatraman R. K., Hassan Tolba A., Solling T., Cibulka R., El-Zohry A.: Ultrafast Events of Photoexcited Iron(III)chloride for Activation of Benzylic C\u2014H Bonds.&nbsp;<i>J. Phys. Chem. Lett.<\/i> <b>2024<\/b>, 15, 6202\u22126208. <a href=\"https:\/\/doi.org\/10.1021\/acs.jpclett.4c01116\">DOI:10.1021\/acs.jpclett.4c01116<\/a><\/span><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\">Weisheitelov\u00e1 I., Varma N., Chudoba J., Burdzi\u0144ski G., Sikorski M., Cibulka R.: Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled by DMSO solvent. Green Chemistry,&nbsp;<strong>2024<\/strong>, <em>26<\/em>, 4880-4887. <a href=\"https:\/\/doi.org\/10.1039\/D4GC00087K\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D4GC00087K<\/a><\/span><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Bure\u0161ov\u00e1 Z., Gobeze H. B., Grygarov\u00e1 M., Pytela O., Klikar M., Obert\u00edk R., Cibulka R., Islam T., Schanze K. S., Bure\u0161 F.: <\/span><span lang=\"EN-US\" style=\"font-size: 12.0pt; mso-ansi-language: EN-US;\">Dicyanopyrazine Photoredox Catalysts: Correlation of Efficiency with Photophysics and Electronic Structure. <i>Journal of Catalysis<\/i> <b>2024<\/b>, <i>430<\/i>, <\/span><span style=\"font-size: 12.0pt;\">115348.&nbsp; <a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2024.115348\" target=\"_blank\" title=\"Persistent link using digital object identifier\" rel=\"noopener\">DOI:10.1016\/j.jcat.2024.115348<\/a><\/span><o:p><\/o:p><\/p>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">Zubov\u00e1 E., Pokluda A. Dvo\u0159\u00e1kov\u00e1 H., Krupi\u010dka M., Cibulka R.: Exploring the Reactivity of Flavins with Nucleophiles Using a Theoretical and Experimental Approach.<em> ChemPlusChem<\/em> <strong>2024<\/strong>, <span>e202300547<\/span>. <a href=\"https:\/\/doi.org\/10.1002\/cplu.202300547\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cplu.202300547<\/a>.<\/span><\/span><\/p>\r\n<h3><\/h3>\r\n<h3>2023<\/h3>\r\n<p class=\"MsoNormal\"><span style=\"font-size: 12.0pt;\">Pavlovska T., Weisheitelov\u00e1 I., Pramthaisong C., Sikorski M., Jahn U., Cibulka R.: Primary and Secondary Amines by Flavin\u2010Photocatalyzed Consecutive Desulfonylation and Dealkylation of Sulfonamides. <i>Adv. Synth. Catal.<\/i><span>&nbsp;<\/span><strong><span class=\"pubYear\">2023<\/span><\/strong><span>,&nbsp;<\/span><em><span class=\"vol\">365<\/span><\/em><span>,&nbsp;<\/span><span class=\"pageFirst\">4662<\/span>. <a href=\"http:\/\/dx.doi.org\/DOI:10.1002\/adsc.202300843\">DOI:10.1002\/adsc.202300843<\/a>.<\/span><\/p>\r\n<p><span>Golczak A., Pruka\u0142a D., Gierszewski M., Cherkas V., Kwiatek D., Kubiak A., Varma N., Pedzi\u0144ski T., Murphree S., Cibulka R., Mr\u00f3wczi\u0144ska L., Kolanovski J. L., Sikorski M.: Tetramethylalloxazines as efficient singlet oxygen photosensitizers and potential redox\u2011sensitive agents. <\/span><i>Scientific Reports<span>&nbsp;<\/span><\/i><b>2023<\/b><span>,<\/span><i><span>&nbsp;<\/span>13<\/i><span>, 13426.&nbsp;<\/span><a href=\"http:\/\/dx.doi.org\/DOI:10.1038\/s41598-023-40536-4\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41598-023-40536-4<\/a><span>.&nbsp;<\/span><\/p>\r\n<p>Insi\u0144ska-Rak M., Golczak A., Gierszewski M., Anwar Z., Cherkas V., Kwiatek D., Sikorska E., Khmelinskii I., Burdzi\u0144ski G., Cibulka R., Mr\u00f3wczy\u0144skag L., Kolanowskic J. L. and Sikorski M.: 5-Deazaalloxazine as photosensitizer of singlet oxygen and potential redox-sensitive agent.&nbsp;<em>Photochem. Photobiol. Sci<\/em>. <strong>2023<\/strong>. <a href=\"http:\/\/dx.doi.org\/DOI:10.1007\/s43630-023-00401-9\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1007\/s43630-023-00401-9<\/a> &nbsp;<\/p>\r\n<p>Pokluda A., Zubova E., Chudoba J., Krupi\u010dka M., Cibulka R.: Catalytic Artificial Nitroalkane Oxidase \u2013 a Way Towards Organocatalytic Umpolung. <em>Org. Biomol. Chem. <\/em><strong>2023<\/strong><em>, 21, 2768 - 2774<\/em>. &nbsp;<a href=\"http:\/\/dx.doi.org\/DOI:10.1039\/D3OB00101F\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1039\/d3ob00101f<\/a>.<\/p>\r\n<h3>2022<\/h3>\r\n<p>\u010cubi\u0148\u00e1k M., Varma N., Oeser P., Pokluda A., Pavlovska T., Cibulka R., Sikorski M., Tobrman T. Tuning the Photophysical Properties of Flavins by Attaching an Aryl Moiety via Direct C\u2013C Bond Coupling. <em>J. Org. Chem.<\/em>&nbsp;<strong>2022<\/strong>. <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.2c02168\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acs.joc.2c02168<\/a><\/p>\r\n<p>Obert\u00edk R., Chudoba J., \u0160turala J., Tar\u00e1bek J., Ludv\u00edkov\u00e1 L., Slanina T., K\u00f6nig B., Cibulka R.: <em>Chem. Eur. J.<\/em> <strong>2022<\/strong>, accepted as <strong>VIP<\/strong><em>. <\/em><a href=\"https:\/\/doi.org\/10.1002\/chem.202202487\" rel=\"follow\">DOI:10.1002\/chem.202202487<\/a>.<\/p>\r\n<p>Pavlovska T., Kr\u00e1l Lesn\u00fd D., Svobodov\u00e1 E., Hoskovcov\u00e1 I., Archipowa N., Kutta R. J., Cibulka R. Tuning Deazaflavins Towards Highly Potent Reducing Photocatalysts Guided by Mechanistic Understanding - Enhancement of the Key Step by the Internal Heavy Atom Effect. <em>Chem. Eur. J.<\/em> <strong>2022<\/strong>, <em>28<\/em>, e20220076. <strong>Hot Paper<\/strong>. <a href=\"http:\/\/doi.org\/10.1002\/chem.202200768\" rel=\"follow\">DOI:10.1002\/chem.202200768<\/a>.<\/p>\r\n<p>Golczak A., Insi\u0144ska-Rak M., Davoudpour A., Saeed D. H., M\u00e9nov\u00e1 P., Mojr V., Cibulka R., Khmelinskii V., Mr\u00f3wczy\u0144ska L., Sikorski M. Photophysical properties of alloxazine derivatives with extended aromaticity \u2013 potential redox sensitive fluorescent probe. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, volume 272, <span>120985, <\/span><strong>2022<\/strong>. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.saa.2022.120985\" rel=\"follow\">DOI: 10.1016\/j.saa.2022.120985<\/a>.<\/p>\r\n<h3>2021<\/h3>\r\n<p>Tolba A. H., Krupi\u010dka M., Chudoba J., Cibulka R.: Amide bond formation via aerobic photooxidative coupling of alde-hydes with amines catalyzed by a riboflavin derivative <span class=\"cit-title\"><i>Org. Lett.<\/i><\/span><span>&nbsp;<\/span><span class=\"cit-year-info\"><span>2021<\/span><\/span><span class=\"cit-volume\">, 23<\/span><span class=\"cit-issue\">, 17<\/span><span class=\"cit-pageRange\">, 6825\u20136830. <\/span><a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.1c02391\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1021\/acs.orglett.1c02391<\/a>.<\/p>\r\n<p>Radek Cibulka (a prof. M. Fraaije z&nbsp;Univerzity v&nbsp;Groningenu) editory knihy \u201eFlavin-Based catalysis\u201c v&nbsp;nakladatelstv\u00ed Wiley-VCH. Z\u00e1rove\u0148 \u010dlenov\u00e9 na\u0161\u00ed skupiny p\u0159ipravili t\u0159i z&nbsp;dvan\u00e1cti kapitol v&nbsp;t\u00e9to knize:<br>Pavlovska, T.; Cibulka, R., Structure and Properties of Flavins. pp 1-27.<br>Cibulka, R.; Fraaije, M. W., Modes of Flavin-Based Catalysis. pp 97-124.<br>Svobodov\u00e1, E.; Cibulka, R., New Applications of Flavin Photocatalysis. pp 265-291.<br><a href=\"https:\/\/www.wiley-vch.de\/en\/areas-interest\/natural-sciences\/chemistry-11ch\/catalysis-11ch4\/flavin-based-catalysis-978-3-527-34834-3\" target=\"_blank\" rel=\"follow noopener\">Wiley-VCH - Flavin-Based Catalysis<\/a><\/p>\r\n<p>Jakubec M., Nov\u00e1k D., Zatloukalov\u00e1 M., S\u00fdkora J., C\u00edsa\u0159ov\u00e1 I., Cibulka R., Favereau L., Crassous J., Bilewicz R., Hrb\u00e1\u010d J., Storch J., \u017d\u00e1dn\u00fd J., Vacek J.: Flavin-Helicene Amphiphilic Hybrids: Synthesis, Characterization, and Preparation of Surface-Supported Films <span>&nbsp;<\/span><i>ChemPlusChem<\/i><span>&nbsp;<\/span><b>2021<\/b><span>,&nbsp;<\/span><i>86<\/i><span>, 982-990<\/span>. <a href=\"http:\/\/dx.doi.org\/10.1002\/cplu.202100092\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1002\/cplu.202100092<\/a>.<\/p>\r\n<p style=\"text-align: left;\">Pokluda A., Anwar Z., Boguschov\u00e1 V., Anusiewicz I., Skurski P., Sikorski M., Cibulka R.: Robust photocatalytic method using ethylene-bridged flavinium salts for the aerobic oxidation of unactivated benzylic substrates <em>Adv. Synth. Catal.<\/em> <strong>2021<\/strong> <em>363<\/em>, 4371-4379. <strong>VIP<\/strong>, <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.202100024\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1002\/adsc.202100024<\/a>.<br><span class=\"oranzova0\"><strong><\/strong><\/span><\/p>\r\n<p style=\"text-align: center;\"><span class=\"oranzova0\"><strong><span class=\"oranzova0\"><span class=\"oranzova0\">&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/adsc.202100748\" target=\"_blank\" rel=\"follow noopener\"><span class=\"\">\u201e<span class=\"\">Cover Feature\u201c<\/span><\/span><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/adsc.202100748\" target=\"_blank\" rel=\"follow noopener\"><span class=\"oranzova0\"><span class=\"\"><\/span><\/span><span class=\"\"><\/span><\/a><\/span><a href=\"https:\/\/doi.org\/10.1002\/adsc.202100748\" target=\"_blank\" rel=\"follow noopener\"><span class=\"cervena0\"><\/span><\/a><\/strong><\/span><\/p>\r\n<p style=\"text-align: left;\">Hartman T., Reisnerov\u00e1 M., Chudoba J., Svobodov\u00e1 E., Archipowa N., Kutta R. J., Cibulka R.: Photocatalytic Oxidative [2+2] Cycloelimination Reactions with Flavinium Salts: Mechanistic Study and Influence of the Catalyst Structure <em>ChemPlusChem<\/em> <strong>2021<\/strong>, <em>86<\/em>, 373\u2013386. <a href=\"http:\/\/dx.doi.org\/10.1002\/cplu.202000767\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1002\/cplu.202000767.<\/a><\/p>\r\n<p style=\"text-align: center;\"><strong><span class=\"oranzova0\"><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><span class=\"oranzova0\"><span class=\"cerna0\">\u201e<span class=\"\">Cover Feature\u201c<\/span><\/span><span class=\"cerna0\"><\/span><\/span><\/a><\/span><\/strong><a href=\"https:\/\/doi.org\/10.1002\/cplu.202100020\" target=\"_blank\" rel=\"follow noopener\"><\/a><\/p>\r\n<p style=\"text-align: left;\"><span class=\"oranzova0\"><span class=\"cerna0\">Eigner, V\u00e1clav and Holakovsk\u00fd, Roman. \"The crystal structure of 2-(4-((carbamimidoylthio)methyl)benzyl)isothiouronium hexafluorophosphate monohydrate, C<sub>10<\/sub>H<sub>17<\/sub>F<sub>6<\/sub>N<sub>4<\/sub>OPS<sub>2<\/sub>\"&nbsp;<i>Zeitschrift f\u00fcr Kristallographie - New Crystal Structures<\/i>, vol. , no. , 2021.&nbsp; <a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0417\" rel=\"follow\">doi.org\/10.1515\/ncrs-2021-0417<\/a><\/span><a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0417\"><\/a><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"oranzova0\"><span class=\"cerna0\"><span>Eigner, V\u00e1clav and Holakovsk\u00fd, Roman. \"Crystal structure of 2-(3-((carbamimidoylthio)methyl)benzyl)isothiouronium hexafluorophosphate monohydrate, C<\/span><sub>10<\/sub><span>H<\/span><sub>17<\/sub><span>F<\/span><sub>6<\/sub><span>N<\/span><sub>4<\/sub><span>OPS<\/span><sub>2<\/sub><span>&nbsp;\"&nbsp;<\/span><i>Zeitschrift f\u00fcr Kristallographie - New Crystal Structures<\/i><span>, vol. , no. , 2021. &nbsp;<\/span><a href=\"https:\/\/doi.org\/10.1515\/ncrs-2021-0418\" rel=\"follow\">doi.org\/10.1515\/ncrs-2021-0418<\/a><\/span><\/span><\/p>\r\n<h3 style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; font-family: ' source_sans_prolight'; font-size: 14pt; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 26px; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 7px 0px 7px 0px; border: 0px none currentColor;\">2020<\/h3>\r\n<p>Graml A., Nevesel\u00fd T., Kutta R.-J., Cibulka R., K\u00f6nig B.: Deazaflavin reductive photocatalysis involves excited semiquinone radicals <em>Nature Comm.<\/em> <strong>2020<\/strong>, <em>11<\/em>, 3174. &nbsp;DOI: 10.1038\/s41467-020-16909-y. <a href=\"https:\/\/rdcu.be\/b47PV\">https:\/\/rdcu.be\/b47PV<\/a><\/p>\r\n<p>Cibulka R.: Strong chemical reducing agents produced by light <em>Nature<\/em> <strong>580<\/strong>, 31-32 (2020). DOI: 10.1038\/d41586-020-00872-1. <a href=\"https:\/\/www.nature.com\/articles\/d41586-020-00872-1\">https:\/\/www.nature.com\/articles\/d41586-020-00872-1<\/a><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px 0px 20px 0px; border: 0px none currentColor;\"><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span style=\"background-color: #ffffff; border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; display: inline; float: none; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">Tolba A. H., V\u00e1vra F., Chudoba J., Cibulka R: Tuning flavin-based photocatalytic systems for application in the mild chemoselective aerobic oxidation of benzylic substrates <em style=\"font-family: ' source_sans_proregular'; font-size: 15px;\">Eur. J. Org. Chem.<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">2020<\/strong>, 1579\u20131585. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201901628\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; text-decoration: underline; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\" rel=\"follow noopener\">DOI:10.1002\/ejoc.201901628<\/a>.&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/toc\/10990690\/2020\/2020\/10\" target=\"_blank\" title=\"Special issue Photochemical synthesis\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; text-decoration: underline; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\" rel=\"follow noopener\"><strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">Special issue Photochemical synthesis<\/strong>.<\/a><\/span><\/span><\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px 0px 20px 0px; border: 0px none currentColor;\"><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span style=\"background-color: #ffffff; border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; display: inline; float: none; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">Schlosser J., Cibulka R., Gro\u00df P., Ihmels H., Mohrschladt C. J.: Visible-light induced di-\u03c0-methane rearrangement of dibenzobarrelene derivatives <em style=\"font-family: ' source_sans_proregular'; font-size: 15px;\">ChemPhotoChem<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">2020<\/strong>, <em style=\"font-family: ' source_sans_proregular'; font-size: 15px;\">4<\/em>, 132. <a href=\"http:\/\/dx.doi.org\/10.1002\/cptc.201900221\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; text-decoration: underline; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\" rel=\"follow noopener\">DOI:10.1002\/cptc.201900221<\/a>.<\/span><\/span><\/span><\/p>\r\n<h3 style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; font-family: ' source_sans_prolight'; font-size: 14pt; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 26px; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 7px 0px 7px 0px; border: 0px none currentColor;\">2019<\/h3>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px 0px 20px 0px; border: 0px none currentColor;\"><span class=\"cerna5\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span style=\"background-color: #ffffff; border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #00add2; display: inline; float: none; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><span class=\"cerna0\">Zelenka, J.; Cibulka, R., <\/span><\/span><\/span><\/span><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\">Roithov\u00e1, J.: <\/span><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\">Flavinium catalyzed photooxidation: Detection and characterization of elusive peroxyflavinium intermediates. <em style=\"font-family: ' source_sans_proregular'; font-size: 15px;\">Angew. Chem. Int. Ed.<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">2019<\/strong>, 58, 15412-15420. <a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201906293\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; text-decoration: underline; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\" rel=\"follow noopener\">DOI:10.1002\/anie.201906293.<\/a> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">VIP&nbsp;<\/strong><\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: center; text-decoration: none; text-indent: 0px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px 0px 20px 0px; border: 0px none currentColor;\"><span class=\"cerna0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646; font-family: ' source_sans_proregular'; font-size: 15px; font-style: inherit; font-variant: normal; font-weight: inherit; letter-spacing: normal; line-height: 1.2; orphans: 2; text-align: left; text-decoration: none; text-indent: -18px; text-transform: none; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; -webkit-text-stroke-width: 0px; white-space: normal; word-spacing: 0px; padding: 0px; margin: 0px; border: 0px none currentColor;\"><strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\"><img src=\"\/images\/215!0\/uzel\/0007830\/0003~~S84vSy1SKMhMLiktSgUA.png\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333; font-family: ' source_sans_probold'; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\" alt=\"cover picture (\u0161\u00ed\u0159ka 215px)\" width=\"215\" height=\"287\"><\/strong><\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\">M\u00e4rz M., Babor M., Cibulka R.: Flavin Catalysis Employing an N(5)-Adduct: An Application in the Aerobic Organocatalytic Mitsunobu Reaction <em>Eur. J. Org. Chem.<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\">2019<\/strong>, <em>20<\/em>, 3264-3268. <a href=\"https:\/\/doi.org\/10.1002\/ejoc.201900397\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\" rel=\"follow\">DOI:10.1002\/ejoc.201900397<\/a>.<\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #000000; font-family: Calibri; font-size: 100%; font-style: inherit; font-weight: inherit; line-height: 1.2; text-align: left; transition-delay: 0s, 0s, 0s, 0s; transition-duration: 200ms, 500ms, 500ms, 500ms; transition-property: color, background-color, border-color, visibility; transition-timing-function: ease, ease, ease, linear; padding: 0px; margin: 0px; border: 0px none currentColor;\">Pokluda A., Kohout M., Chudoba J., Krupi\u010dka M., Cibulka R.: Nitrosobenzene \u2013 Reagent for the Mitsunobu Esterification Reaction <em>ACS Omega<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\">2019<\/strong>, <em>4<\/em>, 5012-5018. <a href=\"https:\/\/doi.org\/10.1021\/acsomega.8b03551\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\" rel=\"follow noopener\">DOI:10.1021\/acsomega.8b03551.<\/a><\/span><\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\"><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\">Valenta L., Kova\u0159\u00ed\u010dek P., Vale\u0161 V., Bastl Z., Drogowska K. A., Verhagen T. A., Cibulka R., Kalb\u00e1\u010d M.: Spatially resolved covalent functionalization patterns on graphene <em>Angew. Chem. Int. Ed.<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\">2019<\/strong>, <em>58<\/em>, 1324-1328. <a href=\"https:\/\/doi.org\/10.1002\/anie.201810119\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\" rel=\"follow noopener\">DOI:10.1002\/anie.201810119<\/a>.<br><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/anie.201810119\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\">https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/anie.201810119<\/a><\/span><\/p>\r\n<p style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\"><span style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\">Zelenka J., Svobodov\u00e1 E., Tar\u00e1bek J., Hoskovcov\u00e1 I., Boguschov\u00e1 V., Bailly S., Sikorski M., Roithov\u00e1 J., Cibulka R.: Combining flavin photocatalysis and organocatalysis: metal-free aerobic oxidation of unactivated benzylic substrates <em>Org. Lett.<\/em> <strong style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #333333;\">2019<\/strong>, <em>21<\/em>, 114-119. <a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b03547\" target=\"_blank\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #464646;\" rel=\"follow noopener\">DOI:10.1021\/acs.orglett.8b03547.&nbsp;<\/a> <span class=\"cervena0\" style=\"border-image-outset: 0; border-image-repeat: stretch; border-image-slice: 100%; border-image-source: none; border-image-width: 1; color: #e64122;\">Highly cited paper (WOS).<\/span><\/span><\/p>\r\n<h3>2018<\/h3>\r\n<p>M\u00e4rz M., Kohout M., Nevesel\u00fd T., Chudoba J., Prukala D., Nizi\u0144ski S., Sikorski M., Burdzi\u0144ski G., Cibulka R.: Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control <em>Org. Biomol. Chem. <\/em><strong>2018<\/strong>, <em>16<\/em>, 6809-6817. <a href=\"https:\/\/doi.org\/10.1039\/C8OB01822G\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1039\/C8OB01822G<\/a>.<\/p>\r\n<p>Holakovsk\u00fd R., Cibulka R., Kone\u010dkov\u00e1 E., M\u00e4rz M.: Zp\u016fsob stanoven\u00ed enantiomern\u00ed \u010distoty chir\u00e1ln\u00edch sulfoxid\u016f pomoc\u00ed 1H NMR anal\u00fdzy, PV 2016-92, \u010d. 307419. Pozn. <strong>2018<\/strong><\/p>\r\n<p>K\u00f6nig B., K\u00fcmmel S., Svobodov\u00e1 E.&nbsp; and Cibulka R.: Flavin photocatalysis, in <em>Physical Sciences Reviews<\/em>, 3 (8), 20170168, ISSN (Online) 2365-659X. <a href=\"https:\/\/doi.org\/10.1515\/psr-2017-0168\" target=\"_blank\" rel=\"follow noopener\">DOI: 10.1515\/psr-2017-0168.<\/a><\/p>\r\n<p class=\"t m0 xed h9 y277 ff1 fs6 fc0 sc0 ls1 ws0\"><span class=\"ff3\"><span class=\"current-selection\">Slav\u00ed\u010dek P., Cibulka R.: A chemici nebudou m\u00edt co \u017er\u00e1t\u2026 (Strojov\u00e9 u\u010den\u00ed v&nbsp;chemii) <em>Vesm\u00edr<\/em> 97, <strong>2018 <\/strong>(5), 300-301.<br><a href=\"https:\/\/vesmir.cz\/cz\/casopis\/archiv-casopisu\/2018\/cislo-5\/a-chemici-nebudou-mit-co-zrat.html\"><span class=\"zelena0\">https:\/\/vesmir.cz\/cz\/casopis\/archiv-casopisu\/2018\/cislo-5\/a-chemici-nebudou-mit-co-zrat.html<\/span><\/a><\/span><\/span><\/p>\r\n<p class=\"t m0 xed h9 y277 ff1 fs6 fc0 sc0 ls1 ws0\"><span class=\"ff3\"><span class=\"current-selection\"><span style=\"font-size: 12.0pt;\">Muchov\u00e1 E., Bezek M., Suchan J., Cibulka R., Slav\u00ed\u010dek P.: <\/span><span style=\"font-size: 12.0pt;\">Molecular Dynamics and Metadynamics Simulations of [2+2] Photocycloaddition <em>Int. J. Quantum Chem. <\/em><strong>2018<\/strong>, <em>118<\/em>, e25534. <\/span><span style=\"font-size: 12pt;\"><a href=\"http:\/\/dx.doi.org\/10.1002\/qua.25534\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/qua.25534<\/a><\/span><\/span><\/span><\/p>\r\n<p class=\"t m0 xed h9 y277 ff1 fs6 fc0 sc0 ls1 ws0\"><span class=\"ff3\"><span class=\"current-selection\">Cu<\/span><span class=\"ff4\"><span class=\"current-selection\">\u0159<\/span><span class=\"current-selection\">\u00ednov<\/span><span class=\"current-selection\">\u00e1<\/span> <span class=\"current-selection\">P.,<\/span> <span class=\"current-selection\">Dr<\/span><span class=\"current-selection\">a<\/span><span class=\"ff4 current-selection\">\u010d<\/span><span class=\"current-selection\">\u00edn<\/span><span class=\"current-selection\">sk\u00fd <\/span><\/span><\/span><span class=\"current-selection\">M.,<\/span> <span class=\"current-selection\">Jakubec<\/span> <span class=\"current-selection\">M, Tlust\u00fd M., Jank\u016f K., Iz\u00e1k P., Holakovsk\u00fd R.:<\/span> <span class=\"current-selection\">Enantioselective<\/span> <span class=\"current-selection\">complexation <\/span><span class=\"current-selection\">of<\/span> <span class=\"current-selection\">1<\/span><span class=\"ff5 current-selection\">\u2010<\/span><span class=\"current-selection\">phenylethanol<\/span> <span class=\"current-selection\">with<\/span> <span class=\"current-selection\">chiral<\/span> <span class=\"current-selection\">comp<\/span><span class=\"current-selection\">ounds<\/span> <span class=\"current-selection\">bearing <\/span><span class=\"current-selection\">urea<\/span> <span class=\"current-selection\">moiety.<\/span> <em><span class=\"ff6\"><span class=\"current-selection\">Chirality<\/span><\/span> <\/em><span class=\"current-selection\"><strong>2018<\/strong>, <em>30, <\/em>79<\/span><span class=\"current-selection\">8<\/span><span class=\"ff5 current-selection\">\u2013<\/span><span class=\"current-selection\">806.&nbsp;<a href=\"http:\/\/doi.org\/10.1002\/chir.22855\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/chir.22855<\/a>.<\/span><\/p>\r\n<p>Mojr V., Pitrov\u00e1 G., Strakov\u00e1 K., Prukala D., Brazevic S., Svobodov\u00e1 E., Hoskovcov\u00e1 I., Burdzi\u0144ski G., Slanina T., Sikorski M., Cibulka R.: Flavin Photocatalysts for&nbsp; visible Light [2+2] Cycloadditions: Structure, Reactivity and Reaction Mechanism <em>ChemCatChem<\/em> <strong>2018<\/strong>, <em>10<\/em>, 849-858. <a href=\"http:\/\/doi.org\/10.1002\/cctc.201701490\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/cctc.201701490<\/a>.<\/p>\r\n<p>Kurfi\u0159t M., \u0160pa\u010dkov\u00e1 J., Svobodov\u00e1 E., Cibulka R.: Flavin derivatives immobilized on mesoporous silica: a versatile tool in visible-light photooxidation reactions <em>Monatshefte<\/em> <em>Chem. <\/em><strong>201<\/strong><strong>8<\/strong>, <em>149<\/em>, 863-869. <a href=\"http:\/\/doi.org\/10.1007\/s00706-017-2127-1\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1007\/s00706-017-2127-1<\/a>.<\/p>\r\n<h3>2017<\/h3>\r\n<p class=\"x_MsoNormal\"><span style=\"font-size: 12.0pt;\">\u017durek J., Svobodov\u00e1 E., \u0160turala J., Dvo\u0159\u00e1kov\u00e1 H., Svoboda J., Cibulka R.: Chiral ethylene-bridged flavinium salts: The stereoselectivity of flavin-10a-hydroperoxide formation and the effect of substitution on the photochemical properties <em>Tetrahedron Asymmetry<\/em> <strong>2017<\/strong>, <em>28<\/em>, 1780-1791, <a href=\"http:\/\/doi.org\/10.1016\/j.tetasy.2017.10.029\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1016\/j.tetasy.2017.10.029<\/a><\/span><\/p>\r\n<p><em><span style=\"font-style: normal;\">Sofer, Z., Luxa, J., Bou\u0161a, D., Sedmidubsk\u00fd, D., Lazar, P., Hartman, T., Hardtdegen, H. and Pumera, M.: The Covalent Functionalization of Layered Black Phosphorus by Nucleophilic Reagents. <em>Angew. Chem. Int. Ed.<\/em> <strong>2017<\/strong><span class=\"ffc fs9\"><span class=\"ls48\"><span class=\"ls0\"><span class=\"ffb\"><span class=\"ffd\"><span class=\"current-selection\">,<\/span> <\/span><\/span><\/span><\/span><\/span><em><span class=\"ffc fs9\"><span class=\"ls48\"><span class=\"ls0\"><span class=\"current-selection\">56<\/span><\/span><\/span><\/span><\/em><\/span><\/em><span style=\"font-style: normal;\"><span class=\"ffc fs9\"><span class=\"ls48\"><span class=\"ls0\"><span class=\"ffd ls48\"><span class=\"current-selection\">, 9<\/span><span class=\"current-selection\">891<\/span><span class=\"current-selection\">\u20139896<\/span><\/span><\/span><\/span><\/span><\/span><em><span style=\"font-style: normal;\">. <a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201705722\" target=\"_blank\" rel=\"follow noopener\">DOI:10.1002\/anie.201705722<\/a><\/span><\/em><\/p>\r\n<p><em><span style=\"font-style: normal;\">M\u00e4rz M., Kohout M., Chudoba J., Cibulka R.: <\/span><\/em>Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light <em>Org. Biomol. Chem.<\/em> <strong><span style=\"font-size: 12.0pt;\">2017<\/span><\/strong><em><span style=\"font-size: 12.0pt;\">, 15<\/span><\/em><span style=\"font-size: 12.0pt;\">, 1970-1975.&nbsp;<\/span> <a href=\"http:\/\/dx.doi.org\/ 10.1039\/C6OB02770A\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C6OB02770A<\/a>,&nbsp;highlighted in <a href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2018\/12March.shtm\"><span class=\"zelena0\">http:\/\/www.organic-chemistry.org\/Highlights\/2018\/12March.shtm<\/span><\/a><\/p>\r\n<p>Kolderov\u00e1, N.; Nevesel\u00fd, T.; \u0160turala, J.; Kucha\u0159, M.; Holakovsk\u00fd, R.; Kohout, M.: Enantioseparation of Chiral Sulfoxides on Amylose-Based Columns: Comparison of Normal Phase Liquid Chromatography and Supercritical Fluid Chromatography.&nbsp;<em>Chromatographia<\/em>&nbsp;<strong>2017<\/strong>, <em>80<\/em>, 547-557. <a href=\"http:\/\/dx.doi.org\/ 10.1007\/s10337-016-3234-6\" target=\"_blank\" rel=\"noopener\">DOI: 10.1007\/s10337-016-3234-6<\/a><\/p>\r\n<p>\u0160pa\u010dkov\u00e1 J., Svobodov\u00e1 E., Hartman T., Stibor I., Kopeck\u00e1 J., Cibulkov\u00e1 J., Chudoba J., Cibulka R.: Visible Light [2+2] Photocycloaddition Mediated by Flavin Derivative Immobilized on Mesoporous Silica, <em>ChemCatChem<\/em> <strong>2017<\/strong>, <span style=\"font-size: 12.0pt;\"><span class=\"ff5\"><em> 9<\/em>, 1177-1181<\/span><\/span>. <a href=\"http:\/\/dx.doi.org\/10.1002\/cctc.201601654\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.201601654<\/a><\/p>\r\n<p>Jir\u00e1sek M., Strakov\u00e1 K., Nevesel\u00fd T., Svobodov\u00e1 E., Rottnerov\u00e1 Z., Cibulka R.: Flavin-Mediated Visible Light <span lang=\"EN-US\">[2+2] Photocycloadditon of Nitrogen and Sulfur-Containing Dienes, <em>Eur. J. Org. Chem. <\/em> <strong>2017<\/strong>, 2139-2146. <\/span><a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201601377\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201601377<\/a><\/p>\r\n<h3>2016<\/h3>\r\n<p>Hartman T., Cibulka R.: Photocatalytic Systems with Flavinium Salts: From Photolyase Models to Synthetic Tool for Cyclobutane Ring Opening, <em>Org. Lett.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 3710-3713.<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.6b01743\" target=\"_blank\" rel=\"noopener\"> DOI:10.1021\/acs.orglett.6b01743<\/a><\/p>\r\n<p><span class=\"cerna0\">B\u00edm, D.; Svobodov\u00e1, E.; Eigner, V.; Rul\u00ed\u0161ek, L.; Hoda\u010dov\u00e1, J.: <\/span><span class=\"cerna0\">Copper(II) and Zinc(II) Complexes of Conformationally Constrained Polyazamacrocycles as Efficient Catalysts for RNA Model Substrate Cleavage in Aqueous Solution at Physiological pH, <\/span><span class=\"cervena0\"><span class=\"cerna0\"><em>Chem. Eur. 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Catal. <\/span><\/em><strong><span lang=\"EN-GB\">2016<\/span><\/strong><span lang=\"EN-GB\">, <em>358<\/em>, 1654\u20131663. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201501123\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.201501123<\/a> <strong>VIP<\/strong>. <br><\/span><\/p>\r\n<p>Holakovsk\u00fd R., Cibulka R., Kone\u010dkov\u00e1 E., M\u00e4rz M.: Mo\u010dovina na b\u00e1zi binaftalenu pro stanoven\u00ed enantiomern\u00ed \u010distoty chir\u00e1ln\u00edch sulfoxid\u016f pomoc\u00ed 1H-NMR anal\u00fdzy. <strong>Patent \u010d. 305 940 (PV: 00710-14)<\/strong><\/p>\r\n<h3>2015<\/h3>\r\n<p>Garc\u00eda, Y. R.; Zelenka, J.; Pabon, Y. V.; Iyer, A.; Bud\u011b\u0161\u00ednsk\u00fd, M.; Kraus, T.; Smith, C. I. E.; Madder, A.: Cyclodextrin\u2013peptide conjugates for sequence specific DNA binding, <em>Org. Biomol. Chem.<\/em> <strong>2015<\/strong>, <em>13<\/em>, 5273\u20135278. <a href=\"http:\/\/dx.doi.org\/10.1039\/C5OB00609K\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C5OB00609K<\/a><\/p>\r\n<p>Bousa, D.; Jankovsky, O.; Sedmidubsky, D.; Luxa, J.; Sturala, J.; Pumera, M.; Sofer, Z.: Mesomeric Effects of Graphene Modified with Diazonium Salts: Substituent Type and Position Influence its Properties, <em>Chem. Eur. J.<\/em> <strong>2015<\/strong>, <em> 21<\/em>, 17728-17738. <a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201502127\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.201502127<\/a><\/p>\r\n<p>Tomanov\u00e1 P., \u0160turala J., Bud\u011b\u0161\u00ednsk\u00fd M., Cibulka R.: <span lang=\"EN-GB\" style=\"color: black;\">A click chemistry approach towards flavin-cyclodextrin conjugates \u2013 bioinspired sulfoxidation catalysts, <em>Molecules<\/em> <strong>2015<\/strong>, <span lang=\"EN-GB\"><em>20<\/em>, 19837-19848. <a href=\"http:\/\/dx.doi.org\/10.3390\/molecules201119667\" target=\"_blank\" rel=\"noopener\">DOI:10.3390\/molecules201119667<\/a><\/span><br><\/span><\/p>\r\n<p>Holakovsk\u00fd R., M\u00e4rz M., Cibulka R.: Urea derivatives based on a 1,1'-binaphthalene skeleton as chiral solvating agents for sulfoxides, <em>Tetrahedron: Asymmetry<\/em> <strong>2015<\/strong>, <em>26<\/em>, 1328-1334. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetasy.2015.10.011\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.tetasy.2015.10.011<\/a><\/p>\r\n<p>Hartman J., \u0160turala J., Cibulka R.: <span lang=\"EN-GB\" style=\"color: black;\">Two-phase Oxidations with Aqueous Hydrogen Peroxide Catalysed by Amphiphilic Pyridinium and Diazinium Salts, <em>Adv. Synth. Catal. <\/em><strong>2015<\/strong>, <span lang=\"EN-GB\"><em>357<\/em>, 3573-3586. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201500687\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.201500687<\/a><\/span><br><\/span><\/p>\r\n<p>Mojr V., Svobodov\u00e1 E., Strakov\u00e1 K., Nevesel\u00fd T., Chudoba J., Dvo\u0159\u00e1kov\u00e1 H., Cibulka R.: <span lang=\"EN-US\" style=\"font-size: 12.0pt;\">Tailoring Flavins for Visible Light Photocatalysis: Organocatalytic [2+2] Cycloadditions Mediated by a Flavin Derivative and Visible Light<\/span><span lang=\"EN-US\">,<\/span><em> Chem. Comm. <\/em><strong>2015<\/strong>,&nbsp;<em>51<\/em>, 12036 \u2013 12039. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/cc\/c5cc01344e#!divAbstract\" target=\"_blank\" title=\"DOI: 10.1039\/C5CC01344E\" rel=\"noopener\"><span style=\"font-size: 12.0pt;\">DOI:10.1039\/C5CC01344E<\/span><\/a><\/p>\r\n<p>Sofer, Z.; Jankovsk\u00fd, O.; \u0160imek, P.; Sedmidubsk\u00fd, D.; \u0160turala, J.; Kosina, J.; Mik\u0161ov\u00e1, R.; Mackov\u00e1, A.; Mikulics, M.; Pumera, M.: Insight into the Mechanism of the Thermal Reduction of Graphite Oxide: Deuterium-Labeled Graphite Oxide Is the Key, <em>ACS Nano<\/em>; <strong>2015<\/strong>, <em>9<\/em>, 5478-5485. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acsnano.5b01463\" target=\"_blank\" rel=\"noopener\">DOI:10.1021\/acsnano.5b01463<\/a><\/p>\r\n<p>\u0160turala J., Boh\u00e1\u010dov\u00e1 S., Chudoba J., Metelkov\u00e1 R., Cibulka R.: Electron-deficient Heteroarenium salts \u2013 an Organocatalytic Tool for Activation of Hydrogen Peroxide in Oxidations, <em>J. Org. Chem.<\/em>, <strong>2015<\/strong>, <em>80<\/em>, 2676-2699. <a href=\"http:\/\/dx.doi.org\/10.1021\/jo502865f\" target=\"_blank\" rel=\"noopener\"> DOI:10.1021\/jo502865f<\/a><\/p>\r\n<p>Cibulka R.: Artificial flavin systems for chemoselective and stereoselective oxidations (Microreview), <em>Eur. J. Org. Chem.<\/em>, <strong>2015<\/strong>, 915-932. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201403275\" target=\"_blank\" rel=\"noopener\"> DOI:10.1002\/ejoc.201403275<\/a> + <a href=\"\/files\/uzel\/0007830\/cover1.pdf\">Cover picture<\/a><\/p>\r\n<h3>2014<\/h3>\r\n<p>Zelenka J., Hartman T. Kl\u00edmov\u00e1 K., Hampl F., Cibulka R.: Phase-transfer catalysis in oxidations based on the covalent bonding of hydrogen peroxide to amphiphilic flavinium salts, <em>ChemCatChem<\/em>, <strong>2014<\/strong>, <em>6<\/em>, 2843-2846. <a href=\"http:\/\/dx.doi.org\/10.1002\/cctc.201402533\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.201402533<\/a><\/p>\r\n<p>Kotou\u010dov\u00e1 H., Strnadov\u00e1 I., Kovandov\u00e1 M., Chudoba J., Dvo\u0159\u00e1kov\u00e1 H., Cibulka R.: Biomimetic aerobic oxidative hydroxylation of arylboronic acids to phenols catalysed by a flavin derivative, <em>Org. Biomol. Chem.<\/em>, <strong>2014<\/strong>, <em>12<\/em>, 2137-2142. <a href=\"http:\/\/dx.doi.org\/10.1039\/C3OB42081G\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C3OB42081G<\/a><\/p>\r\n<h3>2013<\/h3>\r\n<p>M\u00e9nov\u00e1 P., Dvo\u0159\u00e1kov\u00e1 H., Eigner V. Ludv\u00edk J., Cibulka R.: Electron-deficient alloxazinium salts: efficient organocatalysts of mild and chemoselective sulfoxidations with hydrogen peroxide, <em>Adv. Synth. Catal.<\/em>, <strong>2013<\/strong>, <em>355<\/em>, 3451-3462. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201300617\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.201300617<\/a><\/p>\r\n<p>K\u00fcmmel S., Cibulka R., K\u00f6nig B.: \u201cFlavin Photocatalysis\u201d in Chemical Photocatalysis (Burkhard K\u00f6nig, ed.), de Gruyter, Berlin <strong>2013<\/strong>, ISBN: 978-3-11-026924-6.<\/p>\r\n<p>Jurok R., Hoda\u010dov\u00e1 J., Eigner V., Dvo\u0159\u00e1kov\u00e1 H., Setni\u010dka V., Cibulka R.: Planar chiral flavinium salts: Synthesis and evaluation of the effect of substituents on the catalytic efficiency in enantioselective sulfoxidation reactions, <em>Eur. J. Org. Chem.<\/em>, <strong>2013<\/strong>, 7724-7738. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201300847\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201300847<\/a><\/p>\r\n<p>Da\u010fov\u00e1 J., K\u00fcmmel S., Feldmeier C., Cibulkov\u00e1 J., Pa\u017eout R., Maixner J., Gschwind R. M., K\u00f6nig B., Cibulka R.: Aggregation effects in visible light flavin photocatalysts: Synthesis, structure and catalytic activity of 10-arylflavins, <em>Chem. Eur. J.<\/em>, <strong>2013<\/strong>, <em>19<\/em>, 1066-1075. <a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201202488\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.201202488<\/a><\/p>\r\n<h3>2012<\/h3>\r\n<p>Hartman T., Herzig V., Bud\u011b\u0161\u00ednsk\u00fd M., Jind\u0159ich J., Cibulka R., Kraus T.: Flavin-cyclodextrin conjugates: effect of the structure on catalytic activity in enantioselective sulfoxidations, <em>Tetrahedron: Asymmetry<\/em>, <strong>2012<\/strong>, <em>23<\/em>, 1571-1583. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetasy.2012.10.017\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.tetasy.2012.10.017<\/a><\/p>\r\n<p>\u0160turala J., Cibulka R.: Novel synthesis of symmetrical dinitro and diamino Tr\u00f6ger\u2019s base analogues, <em>Eur. J. Org. Chem.<\/em>, <strong>2012<\/strong>, 7066-7074. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201201188\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201201188<\/a><\/p>\r\n<p>Cibulka R., Jurok R.: ORGANOKATALYTICK\u00c9 ENANTIOSELEKTIVN\u00cd OXIDACE SULFID\u016e NA SULFOXIDY, <em>Chemick\u00e9 listy<\/em>, <strong>2012<\/strong>, <em>106<\/em>, 896-902. <a href=\"http:\/\/www.chemicke-listy.cz\/docs\/full\/2012_10_896-902.pdf\">http:\/\/www.chemicke-listy.cz\/docs\/full\/2012_10_896-902.pdf<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Cibulka R.: INSIGHT INTO THE CATALYTIC ACTIVITY OF ALLOXAZINIUM AND ISOALLOXAZINIUM SALTS IN THE OXIDATIONS OF SULFIDES AND AMINES WITH HYDROGEN PEROXIDE, <em>J. Mol. Catal. A: Chemical<\/em>, <strong>2012<\/strong>, <em>363-364<\/em>, 362-370. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molcata.2012.07.012\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.molcata.2012.07.012<\/a><\/p>\r\n<p>Da\u010fov\u00e1 J., Svobodov\u00e1 E., Sikorski M., K\u00f6nig B., Cibulka R.: Photooxidation of sulfides to sulfoxides mediated by tetra-O-acetylriboflavin and visible light. <em>ChemCatChem<\/em>, <strong>2012<\/strong>, <em>4<\/em>, 620-623. <a href=\"http:\/\/dx.doi.org\/10.1002\/cctc.201100372\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.201100372<\/a><\/p>\r\n<p>Tiskov\u00e1 zpr\u00e1va:<a href=\"http:\/\/www.chemistryviews.org\/details\/ezine\/2048673\/Blue_Light_District_Sulfide_Photooxidation.html\">\"Blue Light District: Sulfide Photooxidation\" (ChemistryViews.org)<\/a><\/p>\r\n<h3>2011<\/h3>\r\n<p>Mojr V., Budesinsky M., Cibulka R., Kraus T.: Alloxazine-cyclodextrin conjugates for organocatalytic enantioselective sulfoxidations. <em>Org. Biomol. Chem.<\/em>, <strong>2011<\/strong>, <em>9<\/em>, 7257-7580. <a href=\"http:\/\/dx.doi.org\/10.1039\/C1OB05934C\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C1OB05934C<\/a> + <a href=\"\/files\/uzel\/0007830\/cover3_pdf.pdf\" target=\"_blank\" rel=\"noopener\">Cover picture<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Eigner V., \u010cejka J., Dvo\u0159\u00e1kov\u00e1 H., \u0160anda M., Cibulka R.: Synthesis and structural studies of flavin and alloxazine adducts with O-nucleophiles. <em>J. Mol. Struct. <\/em><strong>2011<\/strong>, <em>1004<\/em>, 178-187. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molstruc.2011.08.002\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.molstruc.2011.08.002<\/a><\/p>\r\n<p>Sayin S., Akkus G. U., Cibulka R., Stibor I., Yilmaz M: Synthesis of Flavin-Calix[4]arene Conjugate Derivatives. <em>Helv. Chim. Acta<\/em> <strong>2011<\/strong>, <em>94<\/em>, 481-485. <a href=\"http:\/\/dx.doi.org\/10.1002\/hlca.201000260\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/hlca.201000260<\/a><\/p>\r\n<p>M\u00e9nov\u00e1 P., Kafka F., Dvo\u0159\u00e1kov\u00e1 H., Gunnoo S., \u0160anda M., Cibulka R.: Pyrazinium Salts as Efficient Organocatalysts of Mild Oxidations with Hydrogen Peroxide. <em>Adv. Synth. Catal.<\/em> <strong>2011<\/strong>, <em>353<\/em>, 865-870. <a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201000906\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.201000906<\/a><\/p>\r\n<h3>2010<\/h3>\r\n<p>Rohl\u00ed\u010dek J. Cibulka R., Cibulkov\u00e1 J., Maixner J., Hu\u0161\u00e1k M.: 10-Methylisoalloxazine-5-oxide from synchrotron powder diffraction data. <em>Acta Cryst.<\/em> <strong>2010<\/strong>, <em>E66<\/em>, o3350\u2013o3351. <a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536810048932\" target=\"_blank\" rel=\"noopener\">DOI:10.1107\/S1600536810048932<\/a><\/p>\r\n<p>Mojr V., Herzig V., Budesinsky M., Cibulka R., Kraus T.: Flavin-cyclodextrin conjugates as catalysts of enantioselective sulfoxidations with hydrogen peroxide in aqueous media. <em>Chem. Comm.<\/em>, <strong>2010<\/strong>, <em>46<\/em>, 7599\u20137601. <a href=\"http:\/\/dx.doi.org\/10.1039\/C0CC02562C\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/C0CC02562C<\/a><\/p>\r\n<p>Kova\u0159\u00ed\u010dek P., Eigner V., Holakovsk\u00fd R.: Ribbon and Pleated Sheet Formation by Anion-Directed Hydrogen Bonding In 1,4-Bis(4,5-dihydro-1<em>H<\/em>-imidazol-2-yl)benzene Salts.<em>Structural Chemistry Communications<\/em>, <strong>2010<\/strong>, <em>Vol. 1<\/em>, <em>No. 1<\/em>, 8-11. <a href=\"http:\/\/www.factumpress.com\/index.php\/scc\/article\/viewFile\/19\/pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/www.factumpress.com\/index.php\/scc\/article\/viewFile\/19\/pdf<\/a><\/p>\r\n<p>Jurok R., Cibulka R., Dvo\u0159\u00e1kov\u00e1 H., Hampl F., Hoda\u010dov\u00e1 J.: Planar Chiral Flavinium Salts - Prospective Catalysts for Enantioselective Sulfoxidation Reactions. <em>Eur. J. Org. Chem.<\/em> <strong>2010<\/strong>, 5217-5224. <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201000592\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/ejoc.201000592<\/a><\/p>\r\n<p>Cibulka R.: Flaviny \u2013 perspektivn\u00ed katalyz\u00e1tory oxidac\u00ed a redukc\u00ed. <em>Chem. Listy<\/em> <strong>2010<\/strong>,<em>104<\/em>, 326-333. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/2010_05_326-333.pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/chemicke-listy.cz\/docs\/full\/2010_05_326-333.pdf<\/a><\/p>\r\n<p>J. Budka, V. Eigner, R. Holakovsk\u00fd, P. Kovar\u00edcek and T. Louzilov\u00e1: 25,26,27,28-Tetrapropoxycalix[4]arene-5,17-dicarbonitrile. <em>Acta Cryst.<\/em> <strong>2010<\/strong>, <em>E66<\/em>, o419-o420. <a href=\"http:\/\/journals.iucr.org\/e\/issues\/2010\/02\/00\/om2307\/om2307.pdf\" target=\"_blank\" rel=\"noopener\">http:\/\/journals.iucr.org\/e\/issues\/2010\/02\/00\/om2307\/om2307.pdf<\/a><\/p>\r\n<p>Ji\u0159\u00ed \u017durek, Radek Cibulka, Hana Dvo\u0159\u00e1kov\u00e1, Ji\u0159\u00ed Svoboda: N<sup>1<\/sup>,N<sup>10<\/sup>-Ethylene-bridged flavinium salts derived from <span class=\"kapitalka\">L<\/span>-valinol: synthesis and catalytic activity in H<sub>2<\/sub>O<sub>2<\/sub>oxidations, <em>Tetrahedron Lett.<\/em> <strong>2010<\/strong>, <em>51<\/em>, 1083-1086. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2009.12.096\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.tetlet.2009.12.096<\/a><\/p>\r\n<h3>2009<\/h3>\r\n<p>M\u00e9nov\u00e1 P., Eigner V., Cibulka R., \u010cejka J., Dvo\u0159\u00e1kov\u00e1 H.: 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione. <em>Acta Cryst.<\/em> <strong>2009<\/strong>, <em>E65<\/em>, o1536\u2013o1537. <a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536809020856\">DOI:10.1107\/S1600536809020856<\/a><\/p>\r\n<p>Cibulka R., Baxov\u00e1 L., Dvo\u0159\u00e1kov\u00e1 H., Hampl F., M\u00e9nov\u00e1 P., Mojr V., Plancq B., Sayin S.: Catalytic effect of alloxazinium and isoalloxazinium salts on oxidation of sulfides with hydrogen peroxide in micellar media. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2009<\/strong>, <em>74<\/em>, 973-993. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc2009030\">DOI:10.1135\/cccc2009030<\/a><\/p>\r\n<h3>2008<\/h3>\r\n<p>Jurok R., Svobodov\u00e1 E., Cibulka R.,Hampl F.: Reactivity in micelles - Are we really able to design micellar catalysts? <em>Collect. Czech. Chem. Commun.<\/em> <strong>2008<\/strong>, <em>73<\/em>, 127-146. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20080127\">DOI:10.1135\/cccc20080127<\/a><\/p>\r\n<h3>2007<\/h3>\r\n<p>Baxov\u00e1 L., Cibulka R., Hampl F.: Organocatalytic sulfoxidation in micellar systems containing amphiphilic flavinium salts using hydrogen peroxide as terminal oxidant. <em>J. Mol. Catal. A.<\/em> <strong>2007<\/strong>, <em>277<\/em>, 53\u201360. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.molcata.2007.07.027\">DOI:10.1016\/j.molcata.2007.07.027<\/a><\/p>\r\n<p>Cibulka R., Svobodov\u00e1 E., K\u00f6nig B., Ludv\u00edk J., Hampl F., Li\u0161ka F.: Studium vyu\u017eit\u00ed n\u011bkter\u00fdch N-donorov\u00fdch ligand\u016f a jejich komplex\u016f s ionty p\u0159echodn\u00fdch kov\u016f. <em>Chem. Listy<\/em> <strong>2007<\/strong>, <em>101<\/em>, 886-894. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/2007_11_886-894.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/2007_11_886-894.pdf<\/a><\/p>\r\n<h3>2006<\/h3>\r\n<p>Celik H., Ekmekci G., Ludv\u00edk J., P\u00edcha J., Zuman P: Electroreduction of aromatic oximes: Diprotonation, adsorption, imine formation, and substituent effects. <em>J. Phys. Chem. B<\/em> <strong>2006<\/strong>, <em>110<\/em>, 6785-6796. <a href=\"http:\/\/dx.doi.org\/10.1021\/jp056808t\">DOI:10.1021\/jp056808t<\/a><\/p>\r\n<p>Kivala M., Cibulka R., Hampl F.: Cleavage of 4-nitrophenyl diphenyl phosphate by isomeric quaternary pyridinium ketoximes - How can structure and lipophilicity of functional surfactants influence their reactivity in micelles and microemulsions?<em>Collect. Czech. Chem. Commun.<\/em> <strong>2006<\/strong>, <em>71<\/em>, 1642-1658. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20061642\">DOI:10.1135\/cccc20061642<\/a><\/p>\r\n<h3>2005<\/h3>\r\n<p>Svobodov\u00e1 E., Cibulka R., Hampl F., \u0160midrkal J., Li\u0161ka F.: Metal ion transport through bulk liquid membrane mediated by cationic ligand surfactants. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2005<\/strong>, <em>70<\/em>, 441-465. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20050441\">DOI:10.1135\/cccc20050441<\/a><\/p>\r\n<p>Chvapil M., Kielar F., Li\u0161ka F., \u0160ilh\u00e1nkov\u00e1 A., Bregel K.: Synthesis and evaluation of long-acting d-penicillamine derivatives. <em>Connective Tissue Research<\/em> <strong>2005<\/strong>, <em>46<\/em>, 242-250. <a href=\"http:\/\/dx.doi.org\/10.1080\/03008200500416690\">DOI:10.1080\/03008200500416690<\/a><\/p>\r\n<p>P\u00edcha J., Ku\u010da K., Kivala M., Kohout M., Cabal J., Li\u0161ka F.: A new group of monoquaternary reactivators of acetylcholinesterase inhibited by nerve agents. <em>J. Enzyme Inhib. Med. Chem.<\/em> <strong>2005<\/strong>, <em>20<\/em>, 233-237. <a href=\"http:\/\/dx.doi.org\/10.1080\/14756360400021858\">DOI:10.1080\/14756360400021858<\/a><\/p>\r\n<h3>2004<\/h3>\r\n<p>P\u00edcha J., Cibulka R., Hampl F., Li\u0161ka F., Pa\u0159\u00edk P., Pytela O.: Reactivity of p-substituted benzaldoximes in the cleavage of <em>p<\/em>-nitrophenyl acetate: kinetic and mechanism.<em>Collect. Czech. Chem. Commun.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 397-413. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20040397\">DOI:10.1135\/cccc20040397<\/a><\/p>\r\n<p>P\u00edcha J., Cibulka R., Li\u0161ka F., Pa\u0159\u00edk P., Pytela O.: Reparametrization and\/or determination of Hammett, inductive, mesomeric and AISE substituent constants for five substituents: N<sup>+<\/sup>(CH<sub>3<\/sub>)<sub>3<\/sub>, CH<sub>2<\/sub>N<sup>+<\/sup>(CH<sub>3<\/sub>)<sub>3<\/sub>, CH<sub>2<\/sub>Py, CH<sub>2<\/sub>SO<sub>2<\/sub>CH<sub>3<\/sub> and PO(OCH<sub>3<\/sub>)<sub>2<\/sub>.<em>Collect. Czech. Chem. Commun.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 2239-2252. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20042239\">DOI:10.1135\/cccc20042239<\/a><\/p>\r\n<p>Wiest O., Harrison C. B., Saettel N. J., Cibulka R., Sax M., K\u00f6nig B.: Design, synthesis and evaluation of a biomimetic artificial photolyase model. <em>J. Org. Chem.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 8183\u20138185. <a href=\"http:\/\/dx.doi.org\/10.1021\/jo0494329\">DOI:10.1021\/jo0494329<\/a><\/p>\r\n<p>Cibulka R., Vasold R. K\u00f6nig B.: Catalytic Photooxidation of 4-Methoxybenzyl alcohol with Flavin Zinc(II) cyclen complex. <em>Chem. Eur. J.<\/em> <strong>2004<\/strong>, <em>10<\/em>, 6223\u20136231. <a href=\"http:\/\/dx.doi.org\/10.1002\/chem.200400232\">DOI:10.1002\/chem.200400232<\/a><\/p>\r\n<h3>2002<\/h3>\r\n<p>Ludvik J., Cibulka R.: Electroreduction of methyl azinyl ketoximes and their Ni(II), Cu(II) and Zn(II) complexes on mercury - correlation with their hydrolytic activity. Proceedings of the Fifth International Manuel M. Baizer Symposium in Honor of Professor Jean Michel Saveant, The 201th Meeting of the Electrochemical Society<strong>2002<\/strong>, Vol. 10, p. 142\u2013146.<\/p>\r\n<h3>2001<\/h3>\r\n<p>Cibulka R., C\u00edsa\u0159ov\u00e1 I., Ondr\u00e1\u010dek J., Li\u0161ka F., Ludv\u00edk J.: Electrochemical Reductions of Ni<sup>2+<\/sup>, Cu<sup>2+<\/sup> and Zn<sup>2+<\/sup> Complexes of Azinyl Methyl Ketoximes on Mercury. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2001<\/strong>, <em>66<\/em>, 170. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20010170\">DOI:10.1135\/cccc20010170<\/a><\/p>\r\n<p>Kotou\u010dov\u00e1 H., Cibulka R., Hampl F., Li\u0161ka F.: Amphiphilic quaternary pyridinium ketoximes as functional hydrolytic micellar catalysts \u2013 does the nucleophilic function position influence their reactivity? <em>J. Mol. Catal.<\/em>, <strong>2001<\/strong>, <em>174<\/em>, 59. <a href=\"http:\/\/dx.doi.org\/10.1016\/S1381-1169(01)00178-9\">DOI:10.1016\/S1381-1169(01)00178-9<\/a><\/p>\r\n<p>Ml\u00ed\u010dkov\u00e1 K., \u0160ebela M., Cibulka R., Fr\u00e9bort I., Pe\u010d P., Li\u0161ka F., Tanizawa K.: Inhibition of copper amine oxidases by pyridine-derived aldoximes and ketoximes. <em>Biochimie <\/em><strong>2001<\/strong>, <em>83<\/em>(11-12), 995\u20131002. <a href=\"http:\/\/dx.doi.org\/10.1016\/S0300-9084(01)01345-1\">DOI:10.1016\/S0300-9084(01)01345-1<\/a><\/p>\r\n<p>Cibulka R., Hampl F., Kotou\u010dov\u00e1 H., P\u00e1v O., \u0160ilh\u00e1nkov\u00e1 A., Li\u0161ka F.: Quaternary ketoximes \u2013 New perspective compounds for hydrolysis of toxic organophosphates.<em>Vojensk\u00e9 zdrav. Listy \u2013 Suplementum-<\/em> <strong>2001<\/strong>, <em>70<\/em>(1), 38\u201340.<\/p>\r\n<p>Cibulka R.: Hydrolytick\u00e9 katalyz\u00e1tory zalo\u017een\u00e9 na komplexech alkyl(pyridin-2-yl)ketoxim\u016f. <em>Chem. Listy<\/em> <strong>2001<\/strong>, <em>95<\/em>, 809\u2013810. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/archiv\/2001\/12-PDF\/809-810.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/archiv\/2001\/12-PDF\/809-810.pdf<\/a><\/p>\r\n<h3>2000<\/h3>\r\n<p>Cibulka R., Hampl F., Kotou\u010dov\u00e1 H., Maz\u00e1\u010d J., Li\u0161ka F.: Quaternary pyridinium ketoximes \u2013 New efficient micellar hydrolytic catalysts. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 227. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20000227\">DOI:10.1135\/cccc20000227<\/a><\/p>\r\n<p>Cibulka R., Li\u0161ka F., Ludv\u00edk J.: Electrochemical reductions of methyl azinyl ketoximes on mercury. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 1630. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20001630\">DOI:10.1135\/cccc20001630<\/a><\/p>\r\n<h3>1999<\/h3>\r\n<p>Cibulka R., Hampl F., \u0160midrkal J. and Li\u0161ka F.: Lipophilic N-[2-hydroxyimino-2-(pyridin-2-yl)ethyl]tialkylammonium salts \u2013 New ligands for metal ion extractions into organic solvents, <em>Tetrahedron Lett.<\/em> <strong>1999<\/strong>, <em>40<\/em>, 6849. <a href=\"http:\/\/dx.doi.org\/10.1016\/S0040-4039(99)01382-9\">DOI:10.1016\/S0040-4039(99)01382-9<\/a><\/p>\r\n<p>Cibulka R., Hampl F., Martinu T., Mazac J., Totevova S., Liska F.: Metal ion chelates of lipophilic alkyl diazinyl ketoximes as hydrolytic catalysts <em>Collect. Czech. Chem. Commun.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 1159. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc19991159\">DOI:10.1135\/cccc19991159<\/a><\/p>\r\n<h3>1998<\/h3>\r\n<p>Cibulka R., Hampl F., Li\u0161ka F.: P\u0159\u00edprava a vyu\u017eit\u00ed amfifiln\u00edch oxim\u016f odvozen\u00fdch od azin\u016f, <em>Chem. listy<\/em> <strong>1998<\/strong>, <em>92(6)<\/em>, 469. <a href=\"http:\/\/chemicke-listy.cz\/docs\/full\/1998_06_469-474.pdf\">http:\/\/chemicke-listy.cz\/docs\/full\/1998_06_469-474.pdf<\/a><\/p>\r\n<p>Kotou\u010dov\u00e1 H., Maz\u00e1\u010d J., Cibulka R., Hampl F. and Li\u0161ka F: Unusual course of the p-nitrophenyl phosphate esters cleavage by 3-hydroxyiminoalkylpyridinium salts in micellar solutions, <em>Chem. Lett.<\/em> <strong>1998<\/strong> <em>(7)<\/em>, 649. <a href=\"http:\/\/dx.doi.org\/10.1246\/cl.1998.649\">DOI:10.1246\/cl.1998.649<\/a><\/p>\r\n<h3>1997<\/h3>\r\n<p>Cibulka R., Dvo\u0159\u00e1k D., Hampl F., Li\u0161ka F.: Metallomicellar hydrolytic catalysts containing ligand surfactants derived from alkyl-2-pyridinylketoxime, <em>Collect. Czech. Chem. Commun.<\/em> <strong>1997<\/strong>, <em>62<\/em>, 1342. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc19971342\">DOI:10.1135\/cccc19971342<\/a><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["38649","39232"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38649":{"idvazba":"149016","nad_uzel":"121051","pod_uzel":"38649","url":"","sablona":"4","nazev":"Cibulka's Group","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"30.01.2026 09:51:00","platne_do":null,"iduzel":"38649","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"39232":{"idvazba":"149015","nad_uzel":"121051","pod_uzel":"39232","url":"","sablona":"20","nazev":"Slider Cibulka - en","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"25.05.2017 15:31:40.176327","platne_do":null,"iduzel":"39232","obsah":null,"class":"slider","autonomni":"0","pod_uzly":["39233","53750","95160","95161"],"poduzly_count":4,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"39233":{"idvazba":"41710","nad_uzel":"39232","pod_uzel":"39233","url":"","sablona":"20","nazev":"slider-en","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"39233","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:36:\"0001~~K87JTEktUkjOTCrNyU5USM0DAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"53750":{"idvazba":"62162","nad_uzel":"39232","pod_uzel":"53750","url":"","sablona":"20","nazev":"lide - en","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"53750","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:56:\"0001~~K87JTEktUnDOTCrNyU5USMsvyVcozi4tyMyrVDAyMDIFAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"95160":{"idvazba":"118048","nad_uzel":"39232","pod_uzel":"95160","url":"","sablona":"20","nazev":"fotochemie - en","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"95160","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:33:\"0001~~K87JTEktUiirrMouzVUwBAA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"95161":{"idvazba":"118049","nad_uzel":"39232","pod_uzel":"95161","url":"","sablona":"20","nazev":"laborato\u0159 - en","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 11:15:00","platne_do":null,"iduzel":"95161","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:33:\"0001~~K87JTEktUiirrMouzVUwAgA.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136576":{"idvazba":"167969","nad_uzel":"121046","pod_uzel":"136576","url":"\/research\/cibulka-old\/research","sablona":"1","nazev":"V\u00fdzkum","_url_prefix":"{\/\/uoch.vscht.cz\/research\/cibulka-old\/research}","poradi":"6","skupina_www":"everyone","platne_od":"12.05.2026 21:28:00","platne_do":null,"iduzel":"136576","obsah":"a:9:{s:5:\"nazev\";s:8:\"Research\";s:9:\"seo_title\";s:7:\"V\u00fdzkum\";s:8:\"seo_desc\";s:7:\"V\u00fdzkum\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:30949:\"<h2 class=\"citation__title\" style=\"text-align: center;\">Deazaalloxazines \u2013 Flavin Derivatives That Provide Reductive Photoredox Catalysis with Inert Substrates<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1002\/chem.202502897\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/chem.202502897<\/a><\/p>\r\n<p>Abstract:<\/p>\r\n<p style=\"text-align: justify;\"><span>Reductive transformations of substances that are difficult to reduce continue to pose challenges for photoredox catalysis. Promising photoreduction catalysts include flavin and deazaflavin derivatives; however, even their reductive abilities are limited for the range of substrates considered \u201cinert\u201d. In this work, we present 5-deazaalloxazines, a new group of deazaflavin analogues that are predisposed to catalyze reductions due to their low reduction potential (down to \u22121.65&nbsp;V vs. SCE) even in the ground state. We studied three series of 5-deazaalloxazines ([i] 5-unsubstituted, [ii] 5-aryldeazaalloxazines, and [iii] 5-trifluoromethyl-5-deazaalloxazines) to determine their photophysical and electrochemical properties and their ability to participate in model photoreduction reactions. From 31 compounds, we selected 1,3-dimethyl-7,8-dimethoxy-5-(<\/span><i>o<\/i><span>-tolyl)-5-deazaalloxazine [<\/span><b>3a(<i>o<\/i>-MePh)<\/b><span>], as it showed, among other things, the highest efficiency in photodehalogenation of&nbsp;<\/span><i>p<\/i><span>-fluoroanisole and was photostable and absorbed in the visible light region, thereby allowing photoreactions using a 400&nbsp;nm LED. Practical applicability was demonstrated in the C\u2500P coupling reaction of electron-rich aryl halides (including chloroanisoles and&nbsp;<\/span><i>p<\/i><span>-fluoroanisole) with trimethyl phosphite, providing an arylation reaction to form dimethyl arylphosphonates, and in the release\/deprotection of amines from the corresponding tosyl and triflylamides.<\/span><\/p>\r\n<p style=\"text-align: center;\" class=\"Head u-font-serif u-h2 u-margin-s-ver\"><img src=\"\/files\/uzel\/0136576\/0011~~MwQA.png\" alt=\"\" width=\"400\" height=\"225\"><\/p>\r\n<p style=\"text-align: justify;\" class=\"Head u-font-serif u-h2 u-margin-s-ver\"><span class=\"title-text\"><span>7,8-Dimethoxy-5-aryl-5-deazaalloxazines (<\/span><b>dAll<\/b><span>) are new class of photostable, visible-light-absorbing flavin derivatives which are strongly reducible upon excitation with 400&nbsp;nm light. It was demonstrated on difficult-to-reduce aryl halides like bromo-, chloro- and fluoroanisoles which were transformed to phosphonates by reductive cross-coupling with trimethyl phosphite or on desulfonylation of sulfonamides to free amines by S\u2500N bond cleavage.<\/span><\/span><\/p>\r\n<hr>\r\n<h2 id=\"screen-reader-main-title\" class=\"Head u-font-serif u-h2 u-margin-s-ver\"><span class=\"title-text\">Redox properties of flavin derivatives: A comparative study<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"title-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2025.147520\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.electacta.2025.147520<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"title-text\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"title-text\"><span>Flavins as cofactors in natural systems as well as their artificial analogues used in catalysis are unique due to their specific redox properties. Our study provides the first direct comparison of the electrochemical behavior of various flavin derivatives: in addition to derivatives of the natural flavins possessing isoalloxazine structure, the experiments were oriented also to their analogues: alloxazines, deazaflavins and flavinium or deazaflavinium salts. We focused on the redox properties of six series of the mentioned flavin types with the stress on the substitution in positions 7 and 8 in connection with the structure of the core using various solvents and electrode materials. In addition to the study by cyclic and rotating disk voltammetry (CV and RDV), we turned our attention on the&nbsp;<\/span><em>in-situ<\/em><span>&nbsp;measurements of EPR spectra of radicals generated electrochemically. Experiments are accompanied by theoretical treatment enabling interpretation of electrochemical data and prediction of redox potential values of newly designed flavin derivatives.<\/span><\/span><\/p>\r\n<p><span class=\"title-text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"c-article-title\" data-test=\"article-title\" style=\"text-align: center;\">Redox-innocent scandium(III) as the sole catalyst in visible light photooxidations<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1038\/s41467-025-63233-4\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41467-025-63233-4<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\"><img src=\"\/files\/uzel\/0136576\/0010~~C04GAA.png\" class=\"img_float_right\" alt=\" \u25f3 Sc (png) \u2192 (origin\u00e1l)\" width=\"300\" height=\"300\">Abstract:<\/p>\r\n<p style=\"text-align: justify;\"><span>In recent years, the catalytic activity of scandium triflate Sc(OTf)<\/span><sub>3<\/sub><span>&nbsp;has attracted significant attention due to its robust Lewis acidity and the oxophilicity of Sc<\/span><sup>3+<\/sup><span>. These features have led to impressive progress in developing diverse organic reactions, including C-C bond formation. The Sc<\/span><sup>3+<\/sup><span>&nbsp;also facilitates single electron transfer in photoinduced reactions either by coordination to an organophotoredox catalyst, which modifies its redox reactivity, or by the formation of a scandium\u2013superoxide anion complex after electron transfer from a light-absorbing redox-active compound. The prior consideration of Sc<\/span><sup>3+<\/sup><span>&nbsp;as a redox-inactive\/innocent metal ion initially hampered the investigation of the possibility of using Sc(OTf)<\/span><sub>3<\/sub><span>&nbsp;as a sole visible light photoredox catalyst. This work demonstrates the use of Sc(OTf)<\/span><sub>3<\/sub><span> as a visible light photocatalyst capable of direct and mild aerobic oxidative C-H functionalisation of aromatic substrates by oxidation of the benzylic position and direct cyanation of the aromatic ring.<\/span><span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\">Deazaflavin-Catalyzed Arylation of White Phosphorus with Aryl Bromides and Chlorides<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"> <a href=\"https:\/\/doi.org\/10.1002\/adsc.70005\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.70005<\/a><\/span><\/p>\r\n<p style=\"text-align: left;\">Abstract:<\/p>\r\n<p style=\"text-align: justify;\">A substantial improvement in the challenging photocatalytic arylation of white phosphorus (P 4) with<br>aryl chlorides and bromides is reported. Using the readily accessible deazaflavin-based photocatalyst o-Me-dFl, valuable triarylphosphines (PAr 3) and tetraarylphosphonium salts ([PAr 4]X, X = Br, Cl) are synthesized from P4 under near UV-LED (365 nm) irradiation in up to 87% combined yield with drastically reduced reaction times compared to previous protocols. 31 P nuclear magnetic resonance spectroscopic monitoring studies and density functional theory calculations provide insights into the reaction pathway. The results represent an important step toward more atom-efficient and economical photocatalytic P4 functionalization reactions.<\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Introduction of flavin anions into photoredox catalysis: Acid-base equilibria of lumichrome allows photoreductions with an anion of an elusive 10-unsubstituted isoalloxazine<\/span><\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D5SC01630D\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC01630D<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Abstract:<\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><img src=\"\/images\/0!0\/uzel\/0015100\/0008~~y08qUnDOSM3VC07O1AMA.gif\" class=\"img_float_right\" alt=\" \u25f3 obr Chem.Sci. (gif) \u2192 (origin\u00e1l)\" width=\"400\" height=\"150\">Flavins have been established as effective catalysts in oxidative photoredox catalysis. Conversely, their use in reductive photocatalysis remains limited, mainly due to the relatively low stability of the transient flavin radicals (semiquinones), which are used in photoreductions. The fully reduced forms of flavins are also disadvantaged in photocatalysis because they absorb light in the UV rather than in the visible region. In this work, we present a new approach for reductive flavin photocatalysis that utilises a flavin (isoalloxazine) anion derived from the elusive 10-unsubstituted 3,7,8-trimethylisoalloxazine, an unstable tautomer of 3-methyllumichrome. We found the conditions under which this isoalloxazine anion is formed by <em>in situ<\/em> deprotonation\/isomerisation from the readily available 3-methyllumichrome and we subsequently used it as a photoredox catalyst in the reductive dehalogenation of activated bromoarenes and their C\u2013P coupling reaction with trimethyl phosphite to form an arylphosphonate. Steady-state and transient absorption spectroscopy, NMR and cyclic voltammetry investigations, together with quantum chemical calculations, showed that the anion of oxidised isoalloxazine has several advantages, compared to other forms of flavins used in photoreductions, such as high stability, even in the presence of oxygen, an absorption maximum in the visible region, thereby allowing the use of excitation light between 470 and 505 nm, and a relatively long-lived singlet excited-state.<\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><strong>Cover picture<\/strong>: <em>Chem. Sci.<\/em>, 2025, 16, 11681. <a href=\"https:\/\/doi.org\/10.1039\/D5SC90144H\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D5SC90144H<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><img src=\"\/files\/uzel\/0136576\/0009~~c84vSy1SKMhMLiktSgUA.png\" alt=\" \u25f3 Cover picture (png) \u2192 (origin\u00e1l)\" width=\"500\" height=\"362\"><\/span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\">Divergent photoreduction of nitroaromatic compounds catalysed by dithienoquinoxaline<\/span><\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"text\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2025.116033\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2025.116033<\/a><o:p><\/o:p><\/span>&nbsp;<\/span><\/p>\r\n<p style=\"text-align: left;\"><span class=\"text\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"text\"><img src=\"\/files\/uzel\/0136576\/\/0007~~M9QtNtIz0A02MDAytDQ1NDcyNTAwsLQw1k1PNIzPKUoHAA.jpg\" class=\"img_float_right\" alt=\" \u25f3 1-s2.0-S0021951725000983-ga1_lrg (jpg) \u2192 (origin\u00e1l)\" width=\"350\" height=\"187\">Nitroaromatic compounds can be conveniently reduced to anilines with the aid of a variety of chemical reductants. However, chemodivergent and chemoselective reduction of functionalized nitroaromatics into valuable nitroso, azo(xy), (hydr)azo and (hydroxyl)amino derivatives remains rather elusive. Electro- and photochemical strategies utilizing various catalytic systems and reaction media have been tested but most have been directed towards individual reduction products. Here, we present the photoredox-enabled chemodivergent reduction of nitroaromatics to nitroso, bis-(<em>N<\/em>,<em>O<\/em>-diacetyl)-<em>N<\/em>-arylhydroxylamine, azoxy, azo and amino derivatives. The developed protocol utilizes a novel photocatalyst, 6,9-dimethoxydithieno[2,3-<em>f<\/em>:3\u2032,2\u2032-<em>h<\/em>]quinoxaline-2,3-dicarbonitrile, and Hantzsch ester\/triethanolamine as reductants. With the single organic photocatalyst, the reaction environment, temperature, time and catalyst loading can be varied to achieve chemodivergent photoreduction of nitroaromatics bearing various functional groups and to access a library of valuable products. The application of this methodology to multigram preparations of molecules of pharmaceutical and industrial relevance highlights its practical utility.<\/span><\/p>\r\n<p style=\"text-align: center;\"><span class=\"text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\">Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids andOligopeptides via Flavin N(5)-iminium Covalent Adducts<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><a href=\"https:\/\/doi.org\/10.1002\/adsc.202401556\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/adsc.202401556<\/a><\/span><\/p>\r\n<p><span style=\"font-size: 12.0pt;\">Abstract:<\/span><\/p>\r\n<p style=\"text-align: justify;\">Flavin co-factors and other flavin derivatives are traditionally associated with one- or two-electron redox reactions. Flavins also form covalent intermediates with a variety of substrates. While extensive attention has focused on reactions at the C(4a) position of the flavin ring, recent interest has shifted toward the dynamic potential of the N(5) atom. In our study, we demonstrate the formation of artificial flavin N(5)-iminium covalent adducts via nucleophilic attack by enolates derived from arylacyl esters at the flavin N(5) position. This interaction mimics the biosynthesis of ether phospholipids catalysed by alkyl-dihydroxyacetone phosphate synthase via an N(5)-FAD iminium adduct formation and fatty acid release. Accordingly, we developed a method for the selective removal of phenacyl and 2-naphthylacetyl protecting groups from the C-terminus of \u03b1-amino acids and di- and tripeptides using biomimetic flavin organocatalysis. Although many approaches are currently available for protection of C-terminus of peptides, their removal often requires harsh conditions, which cause racemization and the loss of optical purity, together with other side reactions. Our method is versatile, mild, orthogonal to most functional and protecting groups and maintains optical purity of \u03b1-amino acids. From general point of view, the method signifies the groundbreaking application of the non-canonical reactivity of flavins in organic synthesis.<\/p>\r\n<p style=\"text-align: justify;\"><span style=\"font-size: 12.0pt;\"><strong><span style=\"font-size: 12.0pt; line-height: 107%; font-family: source_sans_proregular; color: #464646; background: white;\">recognized by Synfacts (<\/span><span style=\"font-family: 'Segoe UI',sans-serif;\">H. Yamamoto and T. Hattori: Synfacts 2025 Vol. 21 Issue 05 Pages 543-543, <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2558-1150\" target=\"_blank\" rel=\"noopener\">DOI: 10.1055\/a-2558-1150<\/a>)<\/span><\/strong><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" style=\"text-align: center;\">Chemoselective Anaerobic Dehydrogenation of Alcohols by Using Visible Light and a Positively Charged Deazaflavin Catalyst Regenerated by Acetonitrile Solvent<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1002\/cctc.202401795\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cctc.202401795<\/a><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span>Three series of novel deazaflavinum salts differing in their substitutions at positions 5 (R&nbsp;=&nbsp;H, phenyl, or mesityl), 7, and 8 (R&nbsp;=&nbsp;OMe, Me, H, or Cl) were synthesized as potential catalysts of a novel chemoselective visible light-mediated anaerobic oxidation of primary and secondary alcohols to carbonyl compounds. This mild procedure uses acetonitrile as a solvent, which acts simultaneously as a sacrificial electron acceptor (in place of the oxygen usually used in photooxidation reactions), and therefore the reaction does not need any additives. Structure and properties-versus-catalytic activity studies identified 5-mesityl-7,8-dimethoxy-3-methyldeazaflavinium chloride (<\/span><b>3a-Cl<\/b><span>) as the most potent catalyst.&nbsp;<\/span><b>3a-Cl<\/b><span>&nbsp;was effective in non-deuterated acetonitrile (CH<\/span><sub>3<\/sub><span>CN), unlike its original 5-phenyl analogue&nbsp;<\/span><b>2a-Cl<\/b><span>, which is efficient only in deuterated solvent (CD<\/span><sub>3<\/sub><span>CN). This difference arises because the regeneration of the&nbsp;<\/span><b>2a-Cl<\/b><span>&nbsp;catalyst is slower in CH<\/span><sub>3<\/sub><span>CN than in CD<\/span><sub>3<\/sub><span>CN. Our method using the optimized&nbsp;<\/span><b>3a-Cl<\/b><span>&nbsp;photocatalyst and CH<\/span><sub>3<\/sub><span>CN as a sacrificial oxidant and solvent in one is a useful addition to synthetic organic chemistry. Anaerobic conditions prevent side oxygenation reactions and overoxidations that usually occur in air or oxygen. This property makes this method suitable for dehydrogenations of alcohols that possess additional group(s) sensitive to oxygenation.<\/span><\/p>\r\n<p><span><img src=\"\/files\/uzel\/0136576\/0006~~y08qAgA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 obr (png) \u2192 (origin\u00e1l)\" width=\"280\" height=\"156\"><br><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span>Chemoselective anaerobic dehydrogenation of primary and secondary alcohols to carbonyl compounds that leaves intact of additional oxygenation-sensitive functional groups is possible using a new flavin catalyst, 400 nm light, and acetonitrile, which acts simultaneously as a solvent and sacrificial oxidant. No other additives needed.<\/span><span><\/span><\/p>\r\n<hr>\r\n<h2 class=\"c-article-title\" data-test=\"article-title\" style=\"text-align: center;\">Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivative<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.1038\/s41598-024-75239-x\" target=\"_blank\" rel=\"noopener\">DOI:10.1038\/s41598-024-75239-x<\/a><\/span><\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: 'Times New Roman'; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><\/span><\/span><\/span>Abstract:<br><span>Incorporation of the trimethoxyphenyl group at position 7 of flavin can drastically change the photophysical properties of flavin. We show unique fast singlet&nbsp;<\/span><sup>1<\/sup><span>(\u03c0,\u03c0*) excited state deactivation pathway through nonadiabatic transition to the&nbsp;<\/span><sup>1<\/sup><span>(n,\u03c0*) excited- state, and subsequent deactivation to the ground electronic state (S<\/span><sub>0<\/sub><span>), closing the photocycle. This mechanism explains the exceptionally weak fluorescence and the short excited\u2013state lifetime for the flavin trimethoxyphenyl derivative and the lack of excited triplet T<\/span><sub>1<\/sub><span>&nbsp;state formation. Full recovery of flavin in its ground state takes place within a 15 ps time window after photoexcitation in a polar solvent such as acetonitrile. According to quantum chemical calculations, the C<\/span><sub>(2)<\/sub><span>-O distance elongates by 0.16 \u00c5 in the&nbsp;<\/span><sup>1<\/sup><span>(n,\u03c0*) state, with respect to the ground state. Intermediate\u2013state structures are predicted by theoretical ab initio calculations and their dynamics are investigated using broadband vis-NIR time-resolved transient absorption and fluorescence up-conversion techniques.<\/span><\/p>\r\n<hr>\r\n<h2 class=\"px-4 pt-6 md:px-6\" style=\"text-align: center;\">A facile three-component route to powerful 5-aryldeazaalloxazine photocatalysts<\/h2>\r\n<p style=\"text-align: center;\"><span style=\"font-size: 12.0pt;\"><span style=\"font-size: 12.0pt; font-family: 'Calibri',sans-serif; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\"><a href=\"https:\/\/doi.org\/10.3762\/bjoc.20.161\" target=\"_blank\" rel=\"noopener\">DOI:10.3762\/bjoc.20.161<\/a><\/span><\/span><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span>Functionalized 5-aryldeazaalloxazines have been successfully synthesised through a one-pot, three-component reaction involving&nbsp;<\/span><i>N,N<\/i><span>-dimethylbarbituric acid, an aromatic aldehyde and aniline. By utilizing readily available reagents, this approach opens up the opportunity for the efficient formation of a variety of 5-aryldeazaalloxazines bearing electron-donating or halogen groups. This practical method is characterised by atom economy and offers a direct route to the introduction of an aryl moiety into the C(5)-position of deazaalloxazines, thereby generating novel catalysts for photoredox catalysis without the need for subsequent purification. Thus, it significantly improves existing approaches.<\/span><\/p>\r\n<p style=\"text-align: center;\"><span><img src=\"https:\/\/www.beilstein-journals.org\/bjoc\/content\/figures\/1860-5397-20-161-graphical-abstract.svg?max-width=550&amp;background=ffffff\" class=\"img-responsive margin-sm-top__small margin-md-top__small\" alt=\"Graphical Abstract\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"article_header-title\" style=\"text-align: center;\" tabindex=\"0\"><span class=\"hlFld-Title\" property=\"headline\">Ultrafast Events of Photoexcited Iron(III) Chloride for Activation of Benzylic C\u2013H Bonds<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"hlFld-Title\" property=\"headline\"><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jpclett.4c01116\" target=\"_blank\" rel=\"noopener\">DOI:10.1021\/acs.jpclett.4c01116<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"hlFld-Title\" property=\"headline\">Abstract:<br><span><img src=\"https:\/\/pubs.acs.org\/cms\/10.1021\/acs.jpclett.4c01116\/asset\/images\/medium\/jz4c01116_0007.gif\" class=\"img_float_right img_fancy_no\" alt=\"Figure 1\" width=\"250\">The usage of rare-earth-metal catalysts in the synthesis of organic compounds is widespread in chemical industries but is limited owing to its environmental and economic costs. However, recent studies indicate that abundant-earth metals like iron(III) chloride can photocatalyze diverse organic transformations using blue-light LEDs. Still, the underlying mechanism behind such activity is debatable and controversial, especially in the absence of ultrafast spectroscopic results. To address this urgent challenge, we performed femtosecond time-resolved electronic absorption spectroscopy experiments of iron(III) chloride in selected organic solvents relevant to its photocatalytic applications. Our results show that the long-lived species [Fe(II) \u2190 Cl<\/span><sup>\u2022<\/sup><span>]* is primarily responsible for both oxidizing the organic substrate and reducing molecular oxygen through the diffusion process, leading to the final product and regenerating the photocatalyst rather than the most widely proposed free chloride radical (Cl<\/span><sup>\u2022<\/sup><span>). Our study will guide the rational design of efficient earth-abundant photocatalysts.<\/span><br><\/span><\/p>\r\n<hr>\r\n<h2 class=\"capsule__title fixpadv--m\" style=\"text-align: center;\">Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled using DMSO as the solvent<\/h2>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/doi.org\/10.1039\/D4GC00087K\" target=\"_blank\" rel=\"noopener\">DOI:10.1039\/D4GC00087K<\/a><\/p>\r\n<p style=\"text-align: justify;\">Abstract:<br><span><img src=\"https:\/\/pubs.rsc.org\/en\/Image\/Get?imageInfo.ImageType=GA&amp;imageInfo.ImageIdentifier.ManuscriptID=D4GC00087K&amp;imageInfo.ImageIdentifier.Year=2024\" class=\"img_float_right img_fancy_no\" alt=\"Graphical abstract: Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled using DMSO as the solvent\" width=\"400\">The drawbacks commonly observed in synthetic methods for alcohol oxidation often stem from the utilization of complex, toxic, hazardous, or waste-producing oxidants. When sensitive or complex substrates bearing several functional groups are to be transformed, the selectivity of oxidation becomes another significant challenge. Herein, a chemoselective and operationally simple catalyst-free and additive-free method is presented for the aerial oxidation of 1-phenylpropargyl and 1-phenylallyl alcohols to their corresponding ketones, requiring only a solvent and visible light irradiation. The crucial role of dimethylsulfoxide (DMSO) as the solvent lies in achieving high chemoselectivity. Singlet oxygen, whose formation is photosensitized by the substrate and the product, is captured by DMSO, thereby preventing the undesired over-oxidation that occurs in other solvents. The application of DMSO to protect the substrate against singlet oxygen represents a novel approach that is potentially applicable to other aerobic photocatalytic processes.<\/span><\/p>\r\n<hr>\r\n<h2 id=\"screen-reader-main-title\" class=\"Head u-font-serif u-h2 u-margin-s-ver\" style=\"text-align: center;\"><span class=\"title-text\">Dicyanopyrazine photoredox catalysts: Correlation of efficiency with photophysics and electronic structure<\/span><\/h2>\r\n<p style=\"text-align: center;\"><span class=\"title-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.jcat.2024.115348\" target=\"_blank\" rel=\"noopener\">DOI:10.1016\/j.jcat.2024.115348<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"title-text\">Abstract:<br><span><img src=\"https:\/\/ars.els-cdn.com\/content\/image\/1-s2.0-S0021951724000617-ga1.jpg\" class=\"img_float_right img_fancy_no\" width=\"300\">Catalytic performance of three structurally-related dicyanopyrazine catalysts has been investigated in three photoredox transformations including deuteration of aldehydes, cross-coupling of iodo-substituted (hetero)aromatic substrates, and \u03b1-hydrogen abstraction from amines followed by annulation to pyrroloquinoline. Significantly different catalytic activity of the photocatalysts has been explained with the aid of electrochemical, spectroscopic, and quantum-chemical methods. Electrochemical measurements pointed to reversible one-electron reduction of the photocatalysts affording the corresponding radical anion, and, therefore, dicyanopyrazines are principally well-suited for reductive quenching cycle. Triplet excited state turned out to be a major excited species employed in photoinduced electron transfer. The measured excited state reduction potentials (<\/span><em>E<\/em><sub>red<\/sub><span>* = +1.88\/+1.43&nbsp;V) classify the (5\u2013methoxy)thiophene-substituted dicyanopyrazines among the organic photocatalysts with high oxidation power, which is in contrast to&nbsp;<\/span><em>N<\/em><span>,<\/span><em>N<\/em><span>-dimethylanilino-substituted photocatalysts. Whereas 5\u2013methoxythiophene photocatalyst forms triplet excited state almost independently on the solvent polarity, transient absorption spectroscopy evidenced the triplet state of&nbsp;<\/span><em>N<\/em><span>,<\/span><em>N<\/em><span>-dimethylanilino derivative only in nonpolar media. Moreover, its subsequent reduction to the corresponding radical anion is chemically cumbersome, which contrast to facile one-electron reduction of both cyano groups of photocatalyst bearing weak 5\u2013methoxythiophene donors. The doublet excited radical anion of the latter proved to be very powerful but short-lived reductant with&nbsp;<\/span><em>E<\/em><sub>ox<\/sub><span>* = \u20132.84&nbsp;V. Its reduction power has been demonstrated in a cross-coupling reaction involving consecutive photoinduced electron transfer to preassociated iodo(hetero)arenes. Hence, bis(5-methoxythiophen-2-yl)-2,3-dicyanopyrazine can be utilized in photoredox catalysis either as powerful oxidant or reductant.<\/span><br><\/span><span class=\"title-text\"><\/span><\/p>\r\n<hr>\r\n<h2 class=\"citation__title\" lang=\"en\" style=\"text-align: center;\">Exploring the Reactivity of Flavins with Nucleophiles Using a Theoretical and Experimental Approach<\/h2>\r\n<p style=\"text-align: center;\"><span class=\"hlFld-Title\"><a href=\"https:\/\/doi.org\/10.1002\/cplu.202300547\" target=\"_blank\" rel=\"noopener\">DOI:10.1002\/cplu.202300547<\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\"><span class=\"hlFld-Title\">Abstract:<br><span>Covalent adducts of flavin cofactors with nucleophiles play an important role in non-canonical function of flavoenzymes as well as in flavin-based catalysis. Herein, the interaction of flavin derivatives including substituted flavins (isoalloxazines), 1,10-ethylene-bridged flavinium salts, and non-substituted alloxazine and deazaflavin with selected nucleophiles was investigated using an experimental and computational approach. Triphenylphosphine or trimethylphosphine, 1-nitroethan-1-ide, and methoxide were selected as representatives of neutral soft, anionic soft, and hard nucleophiles, respectively. The interactions were investigated using UV\/Vis and <\/span><sup>1<\/sup><span>H NMR spectroscopy as well as by DFT calculations. The position of nucleophilic attack estimated using the calculated Gibbs free energy values was found to correspond with the experimental data, favouring the addition of phosphine and 1-nitroethan-1-ide into position N(5) and methoxide into position C(10a) of 1,10-ethylene-bridged flavinium salts. The calculated Gibbs free energy values were found to correlate with the experimental redox potentials of the flavin derivatives tested. These findings can be utilized as valuable tools for the design of artificial flavin-based catalytic systems or investigating the mechanism of flavoenzymes.<\/span><br><\/span><\/p>\r\n<p><span class=\"hlFld-Title\"><span><img src=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/cms\/asset\/cd82f6d2-708c-4669-8efe-d0c3b0139981\/cplu202300547-toc-0001-m.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"Description unavailable\" width=\"450\"><\/span><\/span><\/p>\r\n<p style=\"text-align: center;\" class=\"article_header-title\"><span class=\"hlFld-Title\"><span>The ability of flavin derivatives to add a nucleophile can be quantified and the regioselectivity estimated by Gibbs free energy values calculated by DFT methods. The theoretical data corresponds to the results obtained by&nbsp;<\/span><sup>1<\/sup><span>H NMR and UV\/Vis spectroscopy and to experimental flavin reduction potentials.<\/span><\/span><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38649"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38649":{"idvazba":"149016","nad_uzel":"121051","pod_uzel":"38649","url":"","sablona":"4","nazev":"Cibulka's Group","_url_prefix":null,"poradi":"5","skupina_www":"everyone","platne_od":"30.01.2026 09:51:00","platne_do":null,"iduzel":"38649","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136562":{"idvazba":"171806","nad_uzel":"116995","pod_uzel":"136562","url":"\/research\/kohout","sablona":"58","nazev":"Kohout Research Group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kohout}","poradi":"5","skupina_www":"everyone","platne_od":"25.09.2026 10:18:00","platne_do":null,"iduzel":"136562","obsah":"a:14:{s:5:\"nazev\";s:38:\"Smart Organic Materials research group\";s:9:\"seo_title\";s:21:\"Kohout Research Group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:12:\"Ji\u0159\u00ed T\u016fma\";s:11:\"autor_email\";s:14:\"tumaa@vscht.cz\";s:9:\"submenuno\";s:1:\"1\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:20:\"0008~~Sy_KLy0AAA.jpg\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:928:\"<h1 style=\"text-align: center;\">Smart Organic Materials group<\/h1>\r\n<p style=\"text-align: center;\"><br>Welcome to the website of the Smart Organic Materials group at the Department of Organic Chemistry, UCT Prague! For details on our research areas, please check the <a href=\"kohout\/research\">Research<\/a> section.<\/p>\r\n<h2 style=\"text-align: center;\">We are the founders of one of the first UCT Prague\u2019s spin-off companies!<\/h2>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0136562\/0004~~c0_MyU_OKMrPBQA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Galochrom (jpg) \u2192 (origin\u00e1l)\" width=\"605\" height=\"138\"><a href=\"https:\/\/www.galochrom.com\">www.galochrom.com<\/a><\/p>\r\n<p style=\"text-align: center;\"><a href=\"https:\/\/www.linkedin.com\/company\/galochrom\">www.linkedin.com\/company\/galochrom<\/a><br><br><\/p>\r\n<p style=\"text-align: center;\"><\/p>\r\n<p style=\"text-align: center;\"><\/p>\";s:5:\"obsah\";s:3389:\"<h1>News<\/h1>\r\n<h3>17\/09\/2026<\/h3>\r\n<p><strong>New paper on determination of enantiomers of deschloroketamine and its metabolites is out!<\/strong>&nbsp;<br>A joint research team of our group and BAFA laboratory, led by Natalie Pa\u0161kanov\u00e1, has successfully characterized respective enantiomers of a dissociative psychoactive substance deschloroketamine and its metabolic products using SFC-MS\/MS and capillary zone electrophoresis with UV detection in rat brain tissue.<\/p>\r\n<p><span>Pa\u0161kanov\u00e1, N.; Hrub\u00e1, V.; Fr\u00fchauf, P.; Jur\u00e1sek, B.; Kucha\u0159, M.; \u0158ezanka, P.; Kohout, M. Determination of enantiomers of deschloroketamine and its metabolites in Wistar rat brains. <\/span><i>J. Sep. Sci. <\/i><b>2026<\/b><span>, <\/span><i>49<\/i><span>, e70503.<\/span><br>Read the paper here: <a href=\"https:\/\/doi.org\/10.1002\/jssc.70503\"><span data-olk-copy-source=\"MessageBody\">https:\/\/doi.org\/10.1002\/jssc.70503<\/span><\/a><\/p>\r\n<h3>26\/06\/2026<\/h3>\r\n<p><strong>Magdal\u00e9na Lab\u00edkov\u00e1 received the Special Prize of the Czech Chemical Society as part of the Jean-Marie Lehn Prize in Chemistry 2026!<\/strong>&nbsp;<br>We are very proud of our Ph.D. student Magdal\u00e9na for her magnificent, well-deserved achievement!<\/p>\r\n<p><a href=\"https:\/\/www.linkedin.com\/feed\/update\/urn:li:activity:7477752866464690177\/\">https:\/\/www.linkedin.com\/feed\/update\/urn:li:activity:7477752866464690177\/<\/a><br><br><img src=\"\/images\/0!0\/uzel\/0136562\/0002~~SzQEAA.jpg\" alt=\" \u25f3 a1 (jpg) \u2192 (origin\u00e1l)\" width=\"605\" height=\"403\"><\/p>\r\n<h3>22\/06\/2026<\/h3>\r\n<p><strong>Our research was featured on the cover of JACS Au!&nbsp;<br><\/strong>A joint research led by Luk\u00e1\u0161 Toman\u00edk from the Department of Physical Chemistry, with participation of Ji\u0159\u00ed T\u016fma, that was recently published in the JACS Au journal was selected for the cover of the given journal issue.&nbsp;<br><br>Toman\u00edk L., T\u016fma J., \u00d6hrwall G., Nguyen N. L. L., Credidio B., Slav\u00ed\u010dek P., Winter B., Schewe H. C.: <em>JACS Au<\/em> <strong>2026<\/strong>, <em>6<\/em>, 3349-3355.<br>Read the paper here: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacsau.6c00377\">https:\/\/pubs.acs.org\/doi\/10.1021\/jacsau.6c00377<\/a><br><br><img src=\"\/images\/0!0\/uzel\/0136562\/0003~~SzQCAA.jpg\" alt=\" \u25f3 a2 (jpg) \u2192 (origin\u00e1l)\" width=\"224\" height=\"298\"><\/p>\r\n<h3>17\/06\/2026<\/h3>\r\n<p><strong>Magdal\u00e9na Lab\u00edkov\u00e1 received two poster prizes at the Chiranal 2026 conference!<br><\/strong>Magdal\u00e9na\u2019s excellent work was appreciated by both the official conference committee and the Watrex company. For her astonishing poster presentation, she received prizes for 3rd and 2nd place, respectively.<br><br><img src=\"\/images\/450!0\/uzel\/0136562\/0005~~SzQGAA.jpg\" alt=\" \u25f3 a3 (jpg) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"548\"><\/p>\r\n<h3>15\/06\/2026<\/h3>\r\n<p><strong>The joint team of our group and Galochrom representatives is attending the Chiranal 2026 conference!&nbsp;<\/strong><br>Prof. Michal Kohout, Magdal\u00e9na Lab\u00edkov\u00e1, and Adam Posp\u00ed\u0161il were joined by Galochrom\u2019s CEO Martin Kr\u00e1l and COO Ji\u0159\u00ed T\u016fma at the Advances in Chromatography and Electrophoresis \u2013 Chiranal 2026 in Olomouc.<\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136562\/0006~~SzQBAA.jpg\" class=\"img_float_left\" alt=\" \u25f3 a4 (jpg) \u2192 (origin\u00e1l)\" width=\"466\" height=\"350\"><img src=\"\/images\/0!0\/uzel\/0136562\/0007~~SzQFAA.jpg\" class=\"img_float_left\" alt=\" \u25f3 a5 (jpg) \u2192 (origin\u00e1l)\" width=\"262\" height=\"350\"><\/p>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["142466","136563","136564","136565"],"poduzly_count":4,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":0,"142466":{"idvazba":"175468","nad_uzel":"136562","pod_uzel":"142466","url":"","sablona":"4","nazev":"infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"14.07.2026 12:18:00","platne_do":null,"iduzel":"142466","obsah":"a:8:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:5:\"false\";s:12:\"poddokumenty\";s:5:\"false\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:299:\"<ul>\r\n<li><a href=\"\/research\/kohout\" rel=\"follow\">Home<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/people\" rel=\"follow\">People<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/research\" rel=\"follow\">Research<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/publications\" rel=\"follow\">Publications<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136563":{"idvazba":"175465","nad_uzel":"136562","pod_uzel":"136563","url":"\/research\/kohout\/people","sablona":"49","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kohout\/people}","poradi":"1","skupina_www":"everyone","platne_od":"14.07.2026 13:56:00","platne_do":null,"iduzel":"136563","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:1776:\"<h2>Staff<\/h2>\r\n<p><a href=\"https:\/\/www.researchgate.net\/profile\/Michal-Kohout-2\">Prof. Dr. Michal Kohout<\/a> (group leader)<br><a href=\"https:\/\/www.linkedin.com\/in\/ji%C5%99%C3%AD-t%C5%AFma-5183a9a0\/\">Dr. Ji\u0159\u00ed T\u016fma<\/a> (assistant professor)<br>Dr. V\u00e1clav Kozm\u00edk (assistant professor)<br>Prof. Dr. Ji\u0159\u00ed Svoboda (professor emeritus)<br>Mark\u00e9ta Slabochov\u00e1 (lab technician)<\/p>\r\n<h2>Ph.D. Students<\/h2>\r\n<p>Magdal\u00e9na Lab\u00edkov\u00e1<br>Barbora Jansov\u00e1<br>Jana Pol\u00e1chov\u00e1<br>Adam Posp\u00ed\u0161il<br>Vojt\u011bch Boh\u00e1\u010dek<\/p>\r\n<h2>Students<\/h2>\r\n<p>Samuel Pergl<br>Kyryl Pashchenko<br>Filip Ji\u0159\u00edk<br>Kate\u0159ina D\u011bde\u010dkov\u00e1<br>Hana Kal\u00e1bov\u00e1<br>Jan Holub<br>Maty\u00e1\u0161 Novotn\u00fd<br>Adam Verhulst<br>Ond\u0159ej Petrl\u00edk<br>Magdal\u00e9na Knorrov\u00e1<br>Tom\u00e1\u0161 Novotn\u00fd<br>Natalie Sajtlov\u00e1<\/p>\r\n<h2>Collaborators<\/h2>\r\n<p><a href=\"https:\/\/forschung.boku.ac.at\/en\/researcher\/Hubert-Hettegger-5A850A8B75CA8D30\">Prof. Hubert Hettegger<\/a> (BOKU University Vienna)<br><a href=\"https:\/\/natur.cuni.cz\/osoba?poid=1332075002117212\">Prof. Kv\u011bta Kal\u00edkov\u00e1<\/a> (Charles University Prague)<br><a href=\"https:\/\/www.unipg.it\/personale\/roccaldo.sardella\">Prof. Roccaldo Sardella<\/a> (University of Perugia)<br><a href=\"https:\/\/ricerca.dcci.unipi.it\/domenici-valentina.html\">Prof. Valentina Domenici<\/a> (University of Pisa)<br><a href=\"https:\/\/www.uta.edu\/academics\/faculty\/profile?user=kschug\">Prof. Kevin Shug<\/a> (University of Texas at Arlington)<br><a href=\"https:\/\/www.researchgate.net\/lab\/Leonid-Asnin-Lab\">Prof. Leonid Asnin<\/a> (Perm State University)<br><a href=\"https:\/\/www.fzu.cz\/en\/people\/rndr-vladimira-novotna-csc\">Dr. Vladim\u00edra Novotn\u00e1<\/a>, <a href=\"https:\/\/www.fzu.cz\/en\/people\/ing-alexej-bubnov-phd\">Dr. Alexej Bubnov<\/a> (Institute of Physics, Czech Academy of Sciences)<\/p>\r\n<h2><\/h2>\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:182:\"<h2>Our cherished partners<\/h2>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136563\/0001~~K09Nii9ILCrJSy0qVjACAA.jpg\" alt=\" \u25f3 web_partners 2 (jpg) \u2192 (origin\u00e1l)\" width=\"850\" height=\"480\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["142466"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"142466":{"idvazba":"175468","nad_uzel":"136562","pod_uzel":"142466","url":"","sablona":"4","nazev":"infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"14.07.2026 12:18:00","platne_do":null,"iduzel":"142466","obsah":"a:8:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:5:\"false\";s:12:\"poddokumenty\";s:5:\"false\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:299:\"<ul>\r\n<li><a href=\"\/research\/kohout\" rel=\"follow\">Home<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/people\" rel=\"follow\">People<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/research\" rel=\"follow\">Research<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/publications\" rel=\"follow\">Publications<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136564":{"idvazba":"175464","nad_uzel":"136562","pod_uzel":"136564","url":"\/research\/kohout\/research","sablona":"49","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kohout\/research}","poradi":"2","skupina_www":"everyone","platne_od":"09.09.2026 10:55:00","platne_do":null,"iduzel":"136564","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:171958:\"<h1 style=\"text-align: center;\">Research areas<\/h1>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136564\/0005~~K09Nii9KLU5NLErOiA_wc49PLsovKEhNAQA.png\" style=\"float: left;\" alt=\" \u25f3 web_research_PNG_cropped (png) \u2192 (origin\u00e1l)\" width=\"850\" height=\"316\"><\/p>\r\n<h2><span class=\"oranzova0\">Functionalized liquid crystals<\/span><\/h2>\r\n<p style=\"text-align: justify;\">Liquid crystals (LCs) are fascinating materials forming a wide range of mesophases standing on the boundary of solids and liquids. Such materials in their mesophase adopt partial mobility of the liquid state while preserving anisotropic behaviour of crystals. Their key feature is quick response to external stimuli, such as light, electromagnetic field, and mechanical impulses among others. Therefore, such materials are utilized in various applications including but not limited to LC displays, smart windows, and various types of sensors.&nbsp;<br>In our research, we tune the properties of liquid crystal matrices using a plethora of structural components and functional groups. Azobenzene linking group provides light-controlled switch between LC mesophase and isotropic liquid. Chiral elements result in formation of supramolecular chiral domains that lead to unprecedented applications. And implementation of a magnetic nanoparticle triggers mobility of the mesomorphic molecules in magnetic field.<\/p>\r\n<h3>\u2022 &nbsp; &nbsp;Check our highlighted papers on this topic:<\/h3>\r\n<p style=\"language: cs; line-height: 107%; margin-top: 0pt; margin-bottom: 8.0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">State<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">-independent <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">ionic <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">conductivity<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\"> \u2013 <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">breaking <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">the <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">rules<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\"> in <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">electrochemistry<\/span><\/span><\/p>\r\n<p style=\"language: cs; line-height: 107%; margin-top: 0pt; margin-bottom: 8.0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">J.&nbsp;<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Barclay<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, J. M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Williamson<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, H. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Litt<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, S. J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Cowling<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, K. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Shimizu<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, A. A. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Freitas<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, S. Poppe, J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">\u0160turala<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, Y. Sun, M. Kohout, A.-J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Avestro<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, J. N. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Canonglia<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lopes<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, C. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Groves<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, C. J. Jones, P. R. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">McGonigal<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">State<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">-independent <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ionic <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">conductivity<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Science <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2025<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">390<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, 1254-1258. DOI: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: #595959; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #595959; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1126\/science.adk0786\">10.1126\/science.adk0786<\/a><\/span><\/p>\r\n<p style=\"line-height: 115%; margin-top: 0pt; margin-bottom: 8pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Normally, when liquids solidify, their molecules become locked in place, making it much harder for ions to move and leading to a steep decrease in ionic conductivity. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">In <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">this<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">work<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">we<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">have <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">designed<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">a new class of materials, called <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">state-independent electrolytes<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> (SIEs), that break that rule.<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><\/p>\r\n<p style=\"line-height: 115%; margin-top: 0pt; margin-bottom: 8pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">The team have achieved this result by designing a new class of organic molecular ions with special physical and electronic properties. Each molecule has a flat, disc-shaped centre surrounded by long flexible sidechains\u2014like a wheel with soft bristles. Positive charge is spread out evenly across the molecule by the movement of electrons, which prevents it from tightly binding with its negatively charged partner. This allows the negative ions to move freely, flowing through the side-chains (the \u2018soft bristles\u2019). <\/span><\/p>\r\n<p style=\"line-height: 115%; margin-top: 0pt; margin-bottom: 8pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Then, in the solid state, these organic ions naturally stack on top of each other, forming long rigid columns surrounded by many flexible arms: much like static rollers in a car-wash (see diagram). Despite forming an ordered structure, the flexible side chains still create enough space for the negative ions to continue moving as freely as they would in a liquid. <\/span><\/p>\r\n<p style=\"line-height: 115%; margin-top: 0pt; margin-bottom: 8pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Aptos; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 1.0pt; language: en-GB; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">The result: a dynamic ordered structure that allows the negatively charged ions to move through just as easily in the solid state as in the liquid form, with no sharp decrease in ionic conductivity.<\/span><\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136564\/0006~~83GOL0gsSC0yBAA.png\" alt=\" \u25f3 LC_paper1 (png) \u2192 (origin\u00e1l)\" width=\"1500\" height=\"405\"><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">&nbsp;<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Three<\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> in <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">one<\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> \u2013 <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">efficient <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">functionalization <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">of <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">liquid <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">crystals<\/span><\/p>\r\n<p style=\"margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">A<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Poryvai<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. \u0160mahel, M. \u0160vecov\u00e1, A. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Nemati<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, S. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Shadpour<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, P. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Ulbrich<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, T. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Ogolla<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Liu<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, V. Novotn\u00e1, M. Veverka, J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Vejpravov\u00e1<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> T. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Hegmann<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. Kohout, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chiral<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">magnetic<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">photosensitive <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">liquid <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">crystalline <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">nanocomposites <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">based <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">on <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">multifunctional <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">nanoparticles <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">achiral <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">liquid <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">crystals<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ACS Nano<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2022<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">16<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, 11833-11841. DOI: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1021\/acsnano.1c10594\">https:\/\/doi.org\/10.1021\/acsnano.1c10594<\/a><\/span><\/p>\r\n<p style=\"margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">The self-assembly of liquid crystals is technologically important phenomenon due to the capability of liquid crystals to transmit and amplify information. By inserting a dopant with specific property, the organized liquid crystals adopt the dopant properties and can become chiral, photosensitive, luminescent, etc. Many simple and several bifunctional dopants have already been applied.<\/span><\/p>\r\n<p style=\"margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">In our work, we developed the first trifunctional dopant, inducing chirality, photo<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">responsiveness<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">magnetoresponsivity<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> in a simple liquid crystalline host. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">M<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ultifunctional<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> dopants <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">represent<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">an elegant way of introduction of multifunctionality into simple systems. The design of the target nanomaterial and the synthesis of organic molecules was performed at UCT Prague. Given the complexity of the system, broad international cooperation was required to fully characterize the target materials.<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><img src=\"\/images\/0!0\/uzel\/0136564\/0007~~83GOL0gsSC0yAgA.png\" alt=\" \u25f3 LC_paper2 (png) \u2192 (origin\u00e1l)\" width=\"892\" height=\"334\"><\/span><\/p>\r\n<p>&nbsp;<\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Banana-shaped <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">liquid <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">crystal<\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">s <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">for <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ammonia <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">sensors<\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Self-assembled <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">to <\/span><span style=\"font-size: 18.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">control.<\/span><\/p>\r\n<p style=\"margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">B. Jansov\u00e1, S. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Ganesh<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Moorthy<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. \u0160mahel, E. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lesniewska<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. Kohout, M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Bouvet<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Bent-core <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">liquid <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">crystals<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">-based <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">heterojunctions <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">as <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">gas <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">sensors<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Adv<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. Sensor Res. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2025<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">4<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, e00026. DOI:<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: fr; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">&nbsp;<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1002\/adsr.202500026\">https:\/\/doi.org\/10.1002\/adsr.202500026<\/a><\/span><\/p>\r\n<p style=\"margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; direction: ltr; unicode-bidi: embed; word-break: normal; text-align: justify;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Taking advantage of the <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">filmogenic<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> properties of liquid crystal materials,<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">bilayer heterojunction devices are built by combining them with a molecular<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">semiconductor. Herein, the construction of a novel type of heterojunction<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">sensor by<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">employing bent-core liquid crystals as a<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">sublayer with lutetium <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">bisphthalocyanine<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> as a common top layer is<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">achieved. Thanks to the modified drop casting method employed to deposit<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">the sublayers, the resulting heterojunction devices exhibit a smooth surface,<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">the morphology of the sublayer determining that of the top layer. All prepared<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">devices are sensitive to ammonia, with a limit of detection below 10 ppm<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">some<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> even down to 2 ppm, which is more than satisfactory for controlling ammonia<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">levels in<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">industrial working environments. Moreover, the device<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">s<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> show short response time (t90 = 30 s), which is suitable not only for air quality<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">monitoring but also for applications like security alarm systems.<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><img src=\"\/images\/0!0\/uzel\/0136564\/0008~~83GOL0gsSC0yBgA.png\" alt=\" \u25f3 LC_paper3 (png) \u2192 (origin\u00e1l)\" width=\"1500\" height=\"895\"><\/span><\/p>\r\n<h2><br><span class=\"zelena0\">Chiral stationary phases for HPLC<\/span><\/h2>\r\n<p style=\"text-align: justify;\">One of the most challenging tasks in both synthetic and analytical chemistry is elucidation of optically pure compounds. The most widespread method for separation of racemates and other mixtures of stereoisomers revolves around high performance liquid chromatography (HPLC) with a chiral stationary phase. There is, however, no universal stationary phase that would efficiently separate any racemic mixture. This is especially true in the case of ionized and ionizable compounds where even the most renowned stationary phases typically fail.<br>In our group we design, synthesize, and test our own chiral stationary phases based on various natural compounds. Our aim is to tackle the ongoing problem with separation of polar compounds such as amino acids, short peptides and petidomimetics, oligonucleotides, drugs, narcotics, and other biologically active compounds.<\/p>\r\n<h3>\u2022 &nbsp; &nbsp;Check our highlighted papers on this topic:<\/h3>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">Molecular <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">conformations <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">lead to <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">nonaromatic <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">surprise<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lab\u00edkov\u00e1<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, J. Svoboda, J. T\u016fma, W. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lindner<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. Kohout, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chiral <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">recognition <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">without<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> \u03c0\u2212\u03c0-<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">interactions<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Highly <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">efficient <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">chiral <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">strong <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">cation <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">exchangers <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">lacking <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">an <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">aromatic <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">unit in <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">the <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">molecular <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">structure<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">J. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chromatogr<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. A <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2024<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">1719<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, 464729. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">DOI: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2024.464729\">https:\/\/doi.org\/10.1016\/j.chroma.2024.464729<\/a><\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chirality is ubiquitous in nature. Consequently, living organisms possess essential enzymatic mechanisms that <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">recognise<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> the three-dimensional arrangement of chiral molecules, including pharmaceuticals. For this reason, contemporary drugs are typically administered as single enantiomers rather than as racemates, since one enantiomer is usually active while the other may be inactive or even exert adverse effects.<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 8.0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chiral strong cation exchangers (<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">cSCXs<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">) are efficient chiral stationary phases (CSPs) for <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ionisable<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">ionised<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> substances that cannot be resolved on commercially available CSPs; their structural variations, however, have not yet been thoroughly studied. Chiral recognition has been assumed to rely predominantly on \u03c0\u2013\u03c0 interactions, hydrogen bonding and steric interactions (CSP I). To test this assumption, we designed and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">synthesised<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">cSCXs<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> lacking the aromatic unit, which was replaced by a cyclohexane ring (CSPs III and IV), thereby eliminating \u03c0\u2013\u03c0 interactions entirely. We <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">hypothesised<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> that this structural change would lead to a partial or complete loss of <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">enantiorecognition<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. Surprisingly, the non-aromatic <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">cSCXs<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: Calibri; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> displayed chiral recognition comparable to that of previously described cation-exchange-type CSPs: of the 16 analytes screened, 11 were baseline resolved and 5 partially resolved on CSP I, while the non-aromatic CSP III baseline resolved 10 and partially resolved 6.<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 8.0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><img src=\"\/images\/0!0\/uzel\/0136564\/0010~~8wjwcY4vSCxILTIEAA.png\" alt=\" \u25f3 HPLC_paper1 (png) \u2192 (origin\u00e1l)\" width=\"600\" height=\"233\"><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">&nbsp;<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">When&nbsp;<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">Pirkle <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">meets <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">Lindner<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">: <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">Multimodal <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">mixed<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">-mode <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">chiral <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">columns<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lab\u00edkov\u00e1<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, O. Znam\u00ednko, M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Kloubcov\u00e1<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, W. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lindner<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, T. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Rosenau<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, H. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Hettegger<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. Kohout, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">Multimodal cation exchange-type tyrosine-based chiral stationary phases: Synthesis and applications in high-performance liquid chromatography<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Anal<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chim<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. Acta <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2026<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">1381<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, 344750.<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">DOI: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #0272b1; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #0272B1; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2025.344750\">https:\/\/doi.org\/10.1016\/j.aca.2025.344750<\/a><\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">This work introduces improved tyrosine-based CSPs that effectively integrate donor-acceptor<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\"> part (<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">developed by W. H. Pirkle<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">)<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\"> and cation-exchange functionalities<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\"> (<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">developed by W. Lindner<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">)<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">, rendering them a versatile and powerful addition to the available toolkit for challenging chiral separations.<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\"> <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">A key feature of the synthetic strategy was the efficient covalent immobilization of the chiral selectors onto the silica support&nbsp;<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">via<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">&nbsp;a copper(I)-catalyzed <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">azide<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">-alkyne cycloaddition reaction (<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">click chemistry<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\">).&nbsp;<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: ElsevierGulliver; mso-ascii-font-family: ElsevierGulliver; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: #1f1f1f; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-color: #1F1F1F; mso-style-textfill-fill-alpha: 100.0%;\"><img src=\"\/images\/0!0\/uzel\/0136564\/0009~~8wjwcY4vSCxILTICAA.png\" alt=\" \u25f3 HPLC_paper2 (png) \u2192 (origin\u00e1l)\" width=\"1418\" height=\"454\"><\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">&nbsp;<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">Easy&nbsp;<\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">separation <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">of <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">complex <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">chiral <\/span><span style=\"font-size: 18pt; font-family: Calibri; color: black;\">molecules<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">M. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Lab\u00edkov\u00e1<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, B. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Cerra<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, A. Di Michele, A. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Gioiello<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, F. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Ianni<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, R. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Sardella<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, A. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Carotti<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, M. Kohout, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Novel <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">tyrosinol<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">-based chiral stationary phase for the separation of tetracyclic quinolines active as PXR agonists: Investigating the <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">enantiorecognition<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> mechanism through molecular dynamics<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Anal<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">Chim<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">. Acta <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: bold; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">2026<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-style: italic; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">1388<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: 'Times New Roman'; mso-ascii-theme-font: minor-latin; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, 345083.<\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: Calibri; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">DOI: <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: cs; font-weight: normal; font-style: normal; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2026.345083\">https:\/\/doi.org\/10.1016\/j.aca.2026.345083<\/a><\/span><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: left; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><\/p>\r\n<p style=\"language: cs; margin-top: 0pt; margin-bottom: 0pt; margin-left: 0in; text-align: justify; text-justify: inter-ideograph; direction: ltr; unicode-bidi: embed; mso-line-break-override: none; word-break: normal; punctuation-wrap: hanging;\"><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">In this study, we present the design and synthesis of a novel <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">tyrosinol<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">-based CSP and its application in separating tetracyclic tetrahydroquinoline derivatives that act as <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">pregnane<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> X receptor agonists. The new CSP demonstrated high enantioselectivity and <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">chemoselectivity<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\"> under alkane-alcohol (normal-phase) conditions, enabling baseline resolution of all investigated analytes. The enantiomeric elution order (EEO) was unambiguously determined by combining semipreparative-scale chromatography with electronic circular dichroism (ECD) spectroscopy and time-dependent density functional theory calculations. This integrated approach allowed reliable stereochemical assignment of all separated enantiomers and confirmed the consistency of the EEO across the studied series. Complementary molecular dynamics simulations provided mechanistic insight into <\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">enantiorecognition<\/span><span style=\"font-size: 14.0pt; font-family: Calibri; mso-ascii-font-family: Calibri; mso-fareast-font-family: +mn-ea; mso-bidi-font-family: +mn-cs; mso-ascii-theme-font: minor-latin; mso-fareast-theme-font: minor-fareast; mso-bidi-theme-font: minor-bidi; color: black; mso-color-index: 1; mso-font-kerning: 12.0pt; language: en-US; font-weight: normal; font-style: normal; vertical-align: baseline; mso-text-raise: 0%; mso-style-textfill-type: solid; mso-style-textfill-fill-themecolor: text1; mso-style-textfill-fill-color: black; mso-style-textfill-fill-alpha: 100.0%;\">, revealing hydrogen bonding as the primary interaction driving enantioselectivity, with \u03c0\u2013\u03c0 and \u03c0-cation contacts contributing in a substituent-dependent manner. <\/span><\/p>\r\n<h2><img src=\"\/images\/0!0\/uzel\/0136564\/0011~~8wjwcY4vSCxILTIGAA.png\" alt=\" \u25f3 HPLC_paper3 (png) \u2192 (origin\u00e1l)\" width=\"1500\" height=\"594\"><\/h2>\r\n<h2><br><span class=\"modra0\">Optically active spiropyrans<\/span><\/h2>\r\n<p style=\"text-align: justify;\">Spiropyrans are a specific class of photoswitches \u2013 compounds that undergo reversible change of their structure upon external light stimulus. The unique feature of spiropyrans is their tuneable dual change of both molecular geometry and polarity. Despite their chiral nature, isolation of optically pure spiropyrans is very challenging as they undergo spontaneous racemization.&nbsp;<br>We focus on implementation of auxiliary chiral elements into the spiropyran basic scaffold in order to allow formation of only a single stereoisomer. Such photoswitches can find numerous applications in modern materials, e.g., as smart drug delivery systems, chiral sensors, media for enantioselective solid phase extractions, and chiral photosensitive liquid crystals.<\/p>\r\n<h3>\u2022 &nbsp; &nbsp;Check our highlighted paper on this topic:<\/h3>\r\n<p>Boh\u00e1\u010dek V., Erbenov\u00e1 T., Malina J. D., Kloubcov\u00e1 M., \u0160mahel M., Eigner V., T\u016fma J.:&nbsp;<em>RSC Adv.<\/em> <strong>2024<\/strong>, <em>14<\/em>, 37370-37379. DOI: <a href=\"https:\/\/doi.org\/10.1039\/d4ra07750d\">https:\/\/doi.org\/10.1039\/d4ra07750d<\/a>&nbsp;<\/p>\r\n<p><\/p>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["142466"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"142466":{"idvazba":"175468","nad_uzel":"136562","pod_uzel":"142466","url":"","sablona":"4","nazev":"infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"14.07.2026 12:18:00","platne_do":null,"iduzel":"142466","obsah":"a:8:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:5:\"false\";s:12:\"poddokumenty\";s:5:\"false\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:299:\"<ul>\r\n<li><a href=\"\/research\/kohout\" rel=\"follow\">Home<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/people\" rel=\"follow\">People<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/research\" rel=\"follow\">Research<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/publications\" rel=\"follow\">Publications<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136565":{"idvazba":"175463","nad_uzel":"136562","pod_uzel":"136565","url":"\/research\/kohout\/publications","sablona":"49","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kohout\/publications}","poradi":"3","skupina_www":"everyone","platne_od":"17.09.2026 09:04:00","platne_do":null,"iduzel":"136565","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:55064:\"<h3><strong>Patents<\/strong><\/h3>\r\n<p>M. Lab\u00edkov\u00e1, M. Kohout: Selektor pro multimod\u00e1ln\u00ed chir\u00e1ln\u00ed stacion\u00e1rn\u00ed f\u00e1ze pro kapalinovou chromatografii, multimod\u00e1ln\u00ed stacion\u00e1rn\u00ed f\u00e1ze, zp\u016fsob jejich p\u0159\u00edpravy a jejich pou\u017eit\u00ed, registration Nr.: PV 2025-291, date of submission: 03. 05. 2025<\/p>\r\n<p>J. Ga\u00e1lov\u00e1, F. Yalcinkaya, P. Cu\u0159\u00ednov\u00e1, M. Kohout, I. Stibor, P. Iz\u00e1k:&nbsp;<span>Kompozitn\u00ed chir\u00e1ln\u00ed membr\u00e1na, zp\u016fsob jej\u00ed p\u0159\u00edpravy a zp\u016fsob obohacov\u00e1n\u00ed sm\u011bs\u00ed enantiomer\u016f, patent Nr.: 308513, issue date: 02. 09. 2020.<br><\/span><\/p>\r\n<p><span>&nbsp;<\/span><\/p>\r\n<h3><strong>Publications 2026<\/strong><\/h3>\r\n<ol>\r\n<li class=\"MsoNormal\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\"><span data-olk-copy-source=\"MessageBody\">Pa\u0161kanov\u00e1, N.; Hrub\u00e1, V.; Fr\u00fchauf, P.; Jur\u00e1sek, B.; Kucha\u0159, M.; \u0158ezanka, P.; Kohout, M. Determination of enantiomers of deschloroketamine and its metabolites in Wistar rat brains. <i>J. Sep. Sci.<\/i> <b>2026<\/b>, <i>49<\/i>, e70503.<br><\/span><span><a href=\"https:\/\/doi.org\/10.1002\/jssc.70503\" target=\"_blank\" id=\"OWA9f6b5be0-30ff-b57c-714b-d41dcbfbe9f8\" class=\"x_OWAAutoLink\" title=\"https:\/\/doi.org\/10.1002\/jssc.70503\" rel=\"noopener noreferrer\" data-auth=\"NotApplicable\" data-linkindex=\"0\"><u>https:\/\/doi.org\/10.1002\/jssc.70503<\/u><\/a><\/span><\/span><\/li>\r\n<li class=\"MsoNormal\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Va\u0148k\u00e1tov\u00e1, P.; \u0160mahel, M.; Kub\u00ed\u010dkov\u00e1, A.; Chen, H.-H.; Kohout, M.; Kal\u00edkov\u00e1, K. UHPLC and NMR for monitoring E\u2194Z isomerization in chiral liquid crystalline azobenzene derivatives.&nbsp;<i>Anal. Chim. Acta<\/i> <b>2026<\/b>, <i>1420<\/i>, 345934.<br><\/span><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin;\"><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2026.345934\" target=\"_blank\" title=\"Persistent link using digital object identifier\" rel=\"noopener\"><span class=\"anchor-text\"><span lang=\"EN-GB\" style=\"color: black; mso-color-alt: windowtext; background: white; mso-ansi-language: EN-GB; text-decoration: none; text-underline: none;\">https:\/\/doi.org\/10.1016\/j.aca.2026.345934<\/span><\/span><\/a><\/span><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpFirst\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Cu\u0159\u00ednov\u00e1, P.; Melissa, J.; Cesar, F.; Nicol, A.; Schwan, K.; Kohout, M.; Varrichio, C.; Saleh, A.; Wheelock C. E.; J\u00f3hannesson, G.; Eigner, V.; Tribble, J. R.; Brancale, A.; Williams, P. A. Potent neuronal nicotinamide adenine dinucleotide-boosting tetrahydroquinoxalines: Structure-activity relationships and early drug metabolism and pharmacokinetics evaluation. <i>ACS Med. Chem. Lett.<\/i> <b>2026<\/b>, <i>17<\/i>, 916-924. <br><\/span><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin;\"><a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.6c00058\" target=\"_blank\" rel=\"noopener\"><span lang=\"EN-GB\" style=\"color: black; mso-color-alt: windowtext; border: none windowtext 1.0pt; mso-border-alt: none windowtext 0cm; padding: 0cm; background: white; mso-ansi-language: EN-GB;\">https:\/\/doi.org\/10.1021\/acsmedchemlett.6c00058<\/span><\/a><\/span><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpMiddle\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Lab\u00edkov\u00e1, M.; Cerra, B.; Di Michele, A.; Gioiello, A.; Ianni, F.; Sardella, R.; Carotti, A.; Kohout, M. Novel tyrosinol-based chiral stationary phase for the separation of tetracyclic quinolines active as PXR agonists: Investigating the enantiorecognition mechanism through molecular dynamics. <i>Anal. Chim. Acta<\/i> <b>2026<\/b>, <i>1388<\/i>, 345083.<br><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2026.345083\">https:\/\/doi.org\/10.1016\/j.aca.2026.345083<\/a><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpMiddle\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Lin, X.-Y.; Nipate, D. S.; Chen, S.-K; Harada, M.; Jeng, U.S.; Kohout, M.; Lin, H.-C-; Kitagawa, Y.; Akutagawa, T.; Lee, W.-Y.; Chen, H.-H. Morphology Control in PDVT-10\/DTCP Hybrid Films via Meniscus-Guided Cooperative Crystallization for High-Performance OFETs. <i>ACS Appl. Mater. Interfaces<\/i> <b>2026<\/b>, <i>18<\/i>, 10338-10353. <a href=\"https:\/\/doi.org\/10.1021\/acsami.5c23619\">https:\/\/doi.org\/10.1021\/acsami.5c23619<\/a><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpMiddle\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Cuc, T. T. K.; Wu, T.-C.; Quoc, N. P.; Khang, T. M.; Shunmuga Nainar, S. N.; Hue, B. T. B.; Chuang, W.-T.; Chen, H.-H.; Kohout, M.; Lin, H.-C. Ratiometric Mechano-Fluorescent Elastomers Dually Promoted via Effective Force-Triggered Radicals and Preeminent Toughnesses\/Stretchabilities by Unconventional Shuttling Dimensions of Tetraphenylethylene-Suspended [c2] Daisy Chain Rotaxanes. <i>ACS Materials Au<\/i> <b>2026<\/b>, <i>6<\/i>, 222-235. <br><a href=\"https:\/\/doi.org\/10.1021\/acsmaterialsau.5c00182\">https:\/\/doi.org\/10.1021\/acsmaterialsau.5c00182<\/a><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpMiddle\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Lab\u00edkov\u00e1, M.; Posp\u00ed\u0161il, A.; Znam\u00ednko, O.; Lindner, W.; Bianconi, E.; Cavaliere, G.; Sardella, R.; Carotti, A.; Kohout, M. Enantioseparation of proton pump inhibitors using multimodal chiral cation exchangers. <i>Anal. Bioanal. Chem.<\/i> <b>2026<\/b>. DOI:<br><\/span><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin;\"><a href=\"https:\/\/doi.org\/10.1007\/s00216-026-06565-4\"><span lang=\"EN-GB\" style=\"color: black; mso-color-alt: windowtext; background: white; mso-ansi-language: EN-GB;\">https:\/\/doi.org\/10.1007\/s00216-026-06565-4<\/span><\/a><\/span><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpMiddle\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; color: black; mso-color-alt: windowtext; background: white; mso-ansi-language: EN-GB;\">Batao, J.; Ying, X.; Ling, W.; Kohout, M.; Pasechnik, S.; Hongzhen J. Optically tunable liquid crystals phased array antenna for beam steering at X-band. <i>Electromagnetics<\/i> <b>2026<\/b>, <i>46<\/i>, 790-804.<br><\/span><span style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin;\"><a href=\"https:\/\/doi.org\/10.1080\/02726343.2025.2607510\"><span lang=\"EN-GB\" style=\"color: black; mso-color-alt: windowtext; background: white; mso-ansi-language: EN-GB;\">https:\/\/doi.org\/10.1080\/02726343.2025.2607510<\/span><\/a><\/span><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\"><o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpLast\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Ma\u0159\u00edkov\u00e1, T.; Abualzulof, G. W. A.; Jur\u00e1sek, B.; Kohout, M. Preparative Chiral Resolution of Synthetic Cathinones Using Polysaccharide-Based Chiral Stationary Phases. <i>Methods in Molecular Biology<\/i>, <b>2026<\/b>, <i>2994<\/i>, 145-158. (Book chapter)<o:p><\/o:p><\/span><\/li>\r\n<li class=\"MsoListParagraphCxSpLast\" style=\"text-align: justify; line-height: normal;\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">Lab\u00edkov\u00e1, M.; Znam\u00ednko, O.; Kloubcov\u00e1, M.; Lindner, W.; Rosenau, T.; Hettegger, H.; Kohout, M. applications in hing-performance liquid chromatography. <em>Anal. Chim. Acta<\/em> <strong>2026<\/strong>, <em>1381<\/em>, 344750.<br><\/span><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2025.344750\"><span lang=\"EN-GB\" style=\"mso-bidi-font-family: Calibri; mso-bidi-theme-font: minor-latin; mso-ansi-language: EN-GB;\">https:\/\/doi.org\/10.1016\/j.aca.2025.344750<\/span><\/a><\/li>\r\n<\/ol>\r\n<p class=\"MsoNormal\">&nbsp;<\/p>\r\n<h3><strong>Publications 2025<\/strong><\/h3>\r\n<div>\r\n<ol>\r\n<li>Barclay, J.; Williamson, J. M.; Litt, H.; Cowling, S. J.; Shimizu, K.; Freitas, A. A.; Poppe, S.; \u0160turala, J.; Sun, Y.; Kohout, M.; Avestro, A.-J.; Canonglia Lopes, J. N.; Groves, C.; Jones, J. C.; McGonigal P. R.: State-independent ionic conductivity. <em>Science<\/em> <strong>2025<\/strong>, <em>390<\/em>, 1254-1258.<br><a href=\"https:\/\/doi.org\/10.1126\/science.adk0786\">https:\/\/doi.org\/10.1126\/science.adk0786<\/a>.<\/li>\r\n<li><span style=\"font-size: 16px;\">Vos\u00e1hlov\u00e1, Z.; Pol\u00e1chov\u00e1, J.; Svoboda, J.; Kohout, M.; Kal\u00edkov\u00e1, K.: <\/span>Interaction properties and separation potential of zwitterionic stationary phases in hydrophilic interaction liquid chromatography. <em>J. Chromatogr. Open<\/em><strong> 2025<\/strong>,<em> 8<\/em>, 100258.<br><a href=\"https:\/\/doi.org\/10.1016\/j.jcoa.2025.100258\">https:\/\/doi.org\/10.1016\/j.jcoa.2025.100258<\/a>.<\/li>\r\n<li>Lehrhofer, A. F.; Bacher, M.; Melikhov, I.; Sulaeva, I.; Lindner, W.; Kohout, M.; Kamitakahara, H.; Potthast, A.; Rosenau, T.; Hettegger, H.: Elution revolution: Reversing chiral recognition by swapping D- for L-cellulose. <em>Carbohydr. Polym.<\/em><strong> 2025<\/strong>,<em> 367<\/em>, 123896.<br><span class=\"anchor-text-container\"><span class=\"anchor-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.carbpol.2025.123896\">https:\/\/doi.org\/10.1016\/j.carbpol.2025.123896<\/a>.<br><br><\/span><\/span><\/li>\r\n<li>Jansov\u00e1, B.; Kozm\u00edk, V.; Svoboda, J.; Krupi\u010dka, M.; Pociecha, D.; Be\u010dv\u00e1\u0159, P.; Bouvet, M.; B\u00f6hmov\u00e1, Z.; Novotn\u00e1, V.; Kohout, M.: Design and synthesis of photoresponsive bent-core liquid crystals exhibiting polar smectic phases. <em>Mater. Adv.<\/em> <strong>2025<\/strong>, <em>6<\/em>, 6469-6478.<br><a href=\"https:\/\/doi.org\/10.1039\/d5ma00379b\">https:\/\/doi.org\/10.1039\/d5ma00379b<\/a>.<br><br><\/li>\r\n<li><span style=\"font-size: 16px;\">\u010c\u00ed\u017eek, J.; Lab\u00edkov\u00e1, M.; Drobek, M.; Faur, C.; Mericq, J.P.; Ko\u0161tejn, M.; Hrdli\u010dka, Z.; Stanovsk\u00fd, P.; Florekov\u00e1, J.; Yalcinkaya, F.; Kohout, M.; Iz\u00e1k, P.: <\/span>High-performance enantioselective ion-exchange mixed matrix membranes based on PVDF and EVOH polymers with cinchona-derived chiral silica particles. <em>J. Membr. Sci. <\/em><strong>2025<\/strong>,<em> 733<\/em>, 124376.<br><span class=\"anchor-text-container\"><span class=\"anchor-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.memsci.2025.124376\">https:\/\/doi.org\/10.1016\/j.memsci.2025.124376<\/a><\/span><\/span>.<br><br><\/li>\r\n<li><span style=\"font-size: 16px;\">Jansov\u00e1, B.; Ganesh Moorthy, S.; \u0160mahel, M.; Lesniewska, E.; Kohout, M.; Bouvet, M.:&nbsp;<\/span>Bent-Core Liquid Crystal-Based Heterojunctions as Gas Sensors. <em>Adv. Sensor Res.<\/em> <strong>2025<\/strong>,<em> 4<\/em>, e00026.<br><a href=\"https:\/\/doi.org\/10.1002\/adsr.202500026\">https:\/\/doi.org\/10.1002\/adsr.202500026<\/a>.<br><br><\/li>\r\n<li><span style=\"font-size: 16px;\">Varfaj, I.; Sardella, R.; Klimova A. Y.; Asnin, L. D.; Kohout, M.; Carotti, A.:&nbsp;<\/span>Application of Molecular Dynamic Simulation in the Enantiorecognition Mechanism of the Pharmaceutically Relevant Leu-Phe Dipeptides With Four Zwitterionic Chiral Stationary Phases, <em>J. Sep. Sci.<\/em> <strong>2025<\/strong>, <em>48<\/em>, e70220.<br>\r\n<div class=\"epub-section separator\">\r\n<div class=\"epub-section separator\"><a href=\"https:\/\/doi.org\/10.1002\/jssc.70220\">https:\/\/doi.org\/10.1002\/jssc.70220<\/a>.<br><br><\/div>\r\n<span><\/span><\/div>\r\n<span><\/span><\/li>\r\n<li><span style=\"font-size: 16px;\">Ferenczei, J.; Blahout, V.; Dvo\u0159\u00e1kov\u00e1, H.; Brancale, A.; Cu\u0159\u00ednov\u00e1, P,; Lab\u00edkov\u00e1, M.; Kohout, M.; Setni\u010dka, V.; Perl\u00edkov\u00e1, P.:&nbsp;<\/span>Stereoanalysis of the antiparasitic natural product callunene and its synthetic intermediates. <em>J. Nat. Prod. <\/em><strong>2025<\/strong>, <em>88<\/em>, 723-731.<br><a href=\"https:\/\/doi.org\/10.1021\/acs.jnatprod.4c01424\">https:\/\/doi.org\/10.1021\/acs.jnatprod.4c01424<\/a>.<br><br><\/li>\r\n<li><span style=\"font-size: 16px;\">Lehrhofer, A. F.; Petroni, S.; Bacher, M.; Kohout, M.; Schachamayr, D.; Malyshenko, A.; Rosenau, T.; Cipolla, L.; Hettegger, H.:&nbsp;<\/span>Covalent anchoring of a cellulose per(phenyl carbamate) chiral selector onto silica gel through alkyne-azide click chemistry and its utilization in HPLC. <em>Cellulose<\/em> <strong>2025<\/strong>, <em>32<\/em>, 5247\u20135261.<br><span><a href=\"https:\/\/doi.org\/10.1007\/s10570-025-06497-9\">https:\/\/doi.org\/10.1007\/s10570-025-06497-9<\/a>.<br><br><\/span><\/li>\r\n<li><span style=\"font-size: 16px;\">Yalcinkaya, F.; Vipin, K. V.; Yalcinkaya, B.; Siekierka, A.; Kohout, M.; \u010c\u00ed\u017eek, J.; Iz\u00e1k, P.: <\/span>Parametric study of microporous nanofiber support and thin-film composite membranes for remediation of saline water. <em>J. Ind. Text.<\/em> <strong>2025<\/strong>, <em>55<\/em>, May 2025.<br><br><\/li>\r\n<li><span style=\"font-size: 16px;\">Pa\u0161kanov\u00e1, N.; V\u00e1gnerov\u00e1, M.; Jur\u00e1sek, B.; Mazochov\u00e1, K.; Olejn\u00edkov\u00e1-Ladislavov\u00e1, L.; P\u00e1len\u00ed\u010dek, T.; Kohout, M.; S\u00fdkora, D.; Kucha\u0159, M.:&nbsp;<\/span>Achiral LC-MS\/MS and chiral SFC-MS methods for quantification of methoxphenidine and O-desmethyl-methoxphenidine metabolite in rat serum and brain. <em>J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.<\/em> <strong>2025<\/strong>, <em>1259<\/em>, 124613.<br><a href=\"https:\/\/doi.org\/10.1016\/j.jchromb.2025.124613\">https:\/\/doi.org\/10.1016\/j.jchromb.2025.124613<\/a>.<\/li>\r\n<li><span style=\"font-size: 16px;\">Liang, F.; Jing, H.; Fu, J.; Xiang, Y.; Salamon, P.; \u00c9ber, N.; Buka, A.; Kohout, M.; Li, J.; Chen, J.:&nbsp;<\/span>Controlling diffracted beam-polarization by patterned optical-field in a photosensitive chiral nematic. <em>J. Mol. Liq.<\/em> <strong>2025<\/strong>, <em>420<\/em>, 126814.<br><a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2024.126814\">https:\/\/doi.org\/10.1016\/j.molliq.2024.126814<\/a>.<\/li>\r\n<li><span style=\"font-size: 16px;\">\u010c\u00ed\u017eek, J.; Jandov\u00e1, V.; Stanovsk\u00fd, P.; Hovorka, \u0160.; Yalcinkaya, F.; Kohout, M.; Iz\u00e1k, P.:&nbsp;<\/span>Chiral membranes prepared by ionic interactions between sulfobutylether-\uf062-cyclodextrin and anion-exchange membranes. <em>J. Membr. Sci.<\/em> <strong>2025<\/strong>, <em>717<\/em>, 123592.&nbsp;<br><span class=\"anchor-text-container\"><span class=\"anchor-text\"><a href=\"https:\/\/doi.org\/10.1016\/j.memsci.2024.123592\">https:\/\/doi.org\/10.1016\/j.memsci.2024.123592<\/a><\/span><\/span>.<\/li>\r\n<li><span style=\"font-size: 16px;\">Dob\u0161\u00edkov\u00e1, K.; Kohout, M.; Setni\u010dka, V.:&nbsp;<\/span>Chiral separation and spectroscopic characterization of mefloquine analogues.<em> Spectrochim. Acta A Mol. Biomol. Spectrosc. <\/em><strong>2025<\/strong>, <em>324<\/em>, 124940.<br><a href=\"https:\/\/doi.org\/10.1016\/j.saa.2024.124940\" target=\"_blank\" class=\"anchor doi anchor-primary\" title=\"Persistent link using digital object identifier\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\"><span class=\"anchor-text-container\"><span class=\"anchor-text\">https:\/\/doi.org\/10.1016\/j.saa.2024.124940<\/span><\/span><\/a>.<\/li>\r\n<\/ol>\r\n<\/div>\r\n<div><\/div>\r\n<h3><strong>&nbsp;<\/strong><\/h3>\r\n<h3><strong>Publications 2024<\/strong><\/h3>\r\n<ol>\r\n<li>Fuxov\u00e1, H.; Lab\u00edkov\u00e1, M.; Ivanovsk\u00e1, A.; Eli\u00e1\u0161ov\u00e1, P.; Kub\u016f, M.; Hovorka, \u0160.; P\u0159ibyl, M.; \u010c\u00ed\u017eek, J.; Bart\u016fn\u011bk, V.; Kohout, M.; Iz\u00e1k, P. Zeolite-based chiral ion-exchangers for chromatographic enantioseparations and potential applications in membrane separation processes. <em>Talanta<\/em> <strong>2024<\/strong>, <em>278<\/em>, 126419.<br><a href=\"https:\/\/doi.org\/10.1016\/j.talanta.2024.126419\">https:\/\/doi.org\/10.1016\/j.talanta.2024.126419<\/a>. <br><br><\/li>\r\n<li>Varfaj, I.; Lab\u00edkov\u00e1, M.; Sardella, R.; Hettegger, H.; Lindner, W.; Kohout, M.; Carotti, A. A journey in unraveling the enantiorecognition mechanism of 3,5-dinitrobenzoyl-amino acids with two Cinchona alkaloid-based chiral stationary phases: The power of molecular dynamic simulations. <em>Anal. Chim. Acta<\/em> <strong>2024<\/strong>, <em>1314<\/em>, 342791.<br><a href=\"https:\/\/doi.org\/10.1016\/j.aca.2024.342791\">https:\/\/doi.org\/10.1016\/j.aca.2024.342791<\/a><br><br><\/li>\r\n<li>Tichotov\u00e1, M.; Landovsk\u00fd, T.; Lang, J.; Jeziorowski, S.; Schmidts, V.; Kohout, M.; Babor, M.; Lhot\u00e1k, P.; Thiele, C.M.; Dvo\u0159\u00e1kov\u00e1, H. Enantiodiscrimination of Inherently Chiral Thiacalixarenes by Residual Dipolar Couplings. <em>J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>89<\/em>, 9711-9720.<br><a href=\"https:\/\/doi.org\/10.1021\/acs.joc.2c02594\">https:\/\/doi.org\/10.1021\/acs.joc.2c02594<\/a><br><br><\/li>\r\n<li>Asnin, L.D.; Ziganshina, D.I.; Klimova, Y.A.; Reshetova, E.N.; T\u016fma, J.; Kohout, M. Chiral zwitterionic stationary phases based on Cinchona alkaloids and dipeptides: Application in chiral separation of dipeptides under reversed phase conditions. <em>J. Chromatogr. A <\/em><strong>2024<\/strong>, <em>1726<\/em>, 464966.<br><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2024.464966\">https:\/\/doi.org\/10.1016\/j.chroma.2024.464966<\/a><br><br><\/li>\r\n<li>Pa\u0161kanov\u00e1, N.; Hlavat\u00e1, P.; Jur\u00e1sek, B.; Kucha\u0159, M.; Kohout, M. Tuning parameters of single quadrupole mass detector hyphenated to supercritical fluid chromatography for enantioseparation of synthetic cathinones. <em>J. Chromatogr. Open<\/em> <strong>2024<\/strong>, <em>5<\/em>, 100139.<br><a href=\"https:\/\/doi.org\/10.1016\/j.jcoa.2024.100139\">https:\/\/doi.org\/10.1016\/j.jcoa.2024.100139<\/a><br><br><\/li>\r\n<li>Miliutina, E.; Shilenko, V.; Burtsev, V.; Petkevich, A.; Elashnikov, R.; Buravets, V.; Kolsk\u00e1, Z.; Kohout, M.; \u0160vor\u010d\u00edk, V.; Lyutakov, O. Homochiral Optical Fibers Coated with Nanoscale Films of Metal-Organic Frameworks and Double-Plasmonic Ag and Au for In Situ Enantioselective Detection.<em> ACS Appl. Nano Mater. <\/em><strong>2024<\/strong>, <em>7<\/em>, 9210-9217.<br><a href=\"https:\/\/doi.org\/10.1021\/acsanm.4c00624\">https:\/\/doi.org\/10.1021\/acsanm.4c00624<\/a><br><br><\/li>\r\n<li>Luguo, H.A.O.; Liang, F.; Jing, H.; Xiang, Y.; Salamon, P.; \u00c9ber, N.; Buka, A.; Kohout, M.; Chen, J.; Pei, Y. Control of light polarization by optically-induced-chirality in photosensitive nematic fluids.<em> Opt. Express<\/em> <strong>2024<\/strong>, <em>32<\/em>, 13965-13977.<br><a href=\"https:\/\/doi.org\/10.1364\/OE.522820\">https:\/\/doi.org\/10.1364\/OE.522820<\/a><br><br><\/li>\r\n<li>Lab\u00edkov\u00e1, M.; Svoboda, J.; T\u016fma, J.; Lindner, W.; Kohout, M. Chiral recognition without \u03c0\u2212\u03c0-interactions: Highly efficient chiral strong cation exchangers lacking an aromatic unit in the molecular structure. <em>J. Chromatogr. A<\/em> <strong>2024<\/strong>, <em>1719<\/em>, 464729.<br><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2024.464729\">https:\/\/doi.org\/10.1016\/j.chroma.2024.464729<\/a><br><br><\/li>\r\n<li>Kuncov\u00e1, A.; Svoboda, J.; T\u016fma, J.; Asnin, L.; Schug, K.; Kohout, M. Chiral zwitterionic stationary phases based on Cinchona alkaloids and dipeptides \u2013 design, synthesis and application in chiral separation. <em>J. Chromatogr. A <\/em><strong>2024<\/strong>, <em>1717<\/em>, 464664.<br><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2024.464664\">https:\/\/doi.org\/10.1016\/j.chroma.2024.464664<\/a><br><br><\/li>\r\n<li>Pa\u0161kan, M.; Dob\u0161\u00edkov\u00e1, K.; Kucha\u0159, M.; Setni\u010dka, V.; Kohout, M. Synthesis and absolute configuration of cyclic synthetic cathinones derived from \u03b1-tetralone. <em>Chirality <\/em><strong>2024<\/strong>, <em>36<\/em>, e23646.<br><a href=\"https:\/\/doi.org\/10.1002\/chir.23646\">https:\/\/doi.org\/10.1002\/chir.23646<\/a><br><br><\/li>\r\n<li>Svoboda, J.; Kozm\u00edk, V.; Bajz\u00edkov\u00e1, K.; Kohout, M.; Novotn\u00e1, V.; Podoliak, N.; Pociecha, D.; Gorecka, E. Competing synclinic and anticlinic interactions in smectic phases of bent-core mesogens. <em>J. Mater.&nbsp; Chem. C <\/em><strong>2024<\/strong>, <em>12<\/em>, 10903-10909.<br><a href=\"https:\/\/doi.org\/10.1039\/D4TC01695E\">https:\/\/doi.org\/10.1039\/D4TC01695E<\/a><br><br><\/li>\r\n<li>Be\u010dv\u00e1\u0159, P.; Krystianiak, A.; Ganesh Moorthy, S.; Jansov\u00e1, B.; Kohout, M.; Meunier-Prest, R.; Bouvet, M. Electrosynthesized fluorinated polybithiophenes for ammonia sensing. <em>Mater. Chem. Front<\/em>. <strong>2024<\/strong>, <em>8<\/em>, 2666-2680.<br><a href=\"https:\/\/doi.org\/10.1039\/d4qm00323c\">https:\/\/doi.org\/10.1039\/d4qm00323c<\/a><br><br><\/li>\r\n<li>Chu, Y.; Xiang, Y.; Zhang, W.; Hao, L.; Jiang, B.; Kai, Ch.; Gao, Y.; Yongchuan, H.; Kohout, M. Patch antenna adjustable in frequency based on polymer dispersed liquid crystal. <em>Chin. J. Liq. Cryst. Dis. <\/em><strong>2024<\/strong>, <em>39<\/em>, 17-24.<\/li>\r\n<\/ol>\r\n<h3><strong>&nbsp;<\/strong><\/h3>\r\n<h3><strong>Publications 2023<\/strong><\/h3>\r\n<ol>\r\n<li>Jur\u00e1\u0161ek, M.; Kratochv\u00edl, B.; Kohout, M.; \u0160vec, F.; Dra\u0161ar, P. On the separation and strengthening of the image behind the mirror (Deracemization and chirality amplification). <em>Chem. listy <\/em><strong>2023<\/strong>, <em>117<\/em>, 671-676.&nbsp;<br><br><\/li>\r\n<li>Valderhaug, S.; Pa\u0161kanov\u00e1, N.; T\u016fma, J.; Hercikov\u00e1, J.; Eigner, V.; Liu, H.; Gorovoy, A.; Johansen, J. E.; Gautun, O. R. Synthesis, identification, chiral separation and crystal structure of (3R,4R,7S,8S)-3,4,7,8-tetrachlorodecane and its stereoisomers. <em>Heliyon<\/em> <strong>2023<\/strong>, <em>9<\/em>, e16987.<br><a href=\"https:\/\/doi.org\/10.1016\/j.heliyon.2023.e16987\">https:\/\/doi.org\/10.1016\/j.heliyon.2023.e16987<\/a><br><br><\/li>\r\n<li>Jur\u00e1sek, B.; Fagan, P.; Dolensk\u00fd, B.; Pa\u0161kanov\u00e1, N.; Dob\u0161\u00edkov\u00e1, K.; Raich, I.; Jurok, R.; Setni\u010dka, V.; Kohout, M.; \u010cejka, J.; Kucha\u0159, M. A structural spectroscopic study of dissociative anaesthetic methoxphenidine. <em>New J. Chem<\/em><strong>.<\/strong> <strong>2023<\/strong>, <em>47<\/em>, 4543.<br><a href=\"https:\/\/doi.org\/10.1039\/d2nj06126k\" target=\"_blank\" rel=\"noopener\">https:\/\/doi.org\/10.1039\/d2nj06126k<\/a><br><br><\/li>\r\n<li>Dob\u0161\u00edkov\u00e1, K.; Javorsk\u00e1, \u017d.; Pa\u0161kan, M.; Sp\u00e1lovsk\u00e1, D.; Trembul\u00e1kov\u00e1, P.; Hercikov\u00e1, J.; Kucha\u0159, M.; Kozm\u00edk, V.; Kohout, M.; Setni\u010dka, V. Enantioseparation and a comprehensive spectroscopic analysis of novel synthetic cathinones laterally substituted with a trifluoromethyl group. <em>Spectrochim. Acta, Part A,<\/em><strong> 2023<\/strong>, <em>291,<\/em> 122320.<br><a href=\"https:\/\/doi.org\/10.1016\/j.saa.2023.122320\" target=\"_blank\" class=\"anchor doi anchor-default anchor-external-link\" title=\"Persistent link using digital object identifier\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\"><span class=\"anchor-text\">https:\/\/doi.org\/10.1016\/j.saa.2023.122320<\/span><\/a><\/li>\r\n<\/ol>\r\n<h3><strong>&nbsp;<\/strong><\/h3>\r\n<h3><strong>Publications 2022<\/strong><\/h3>\r\n<ol>\r\n<li>Pa\u0161kan, M.; Rimpelov\u00e1, S.; Svobodov\u00e1 Pavl\u00ed\u010dkov\u00e1, V.; Sp\u00e1lovsk\u00e1, D.; Setni\u010dka, V.; Kucha\u0159, M.; Kohout, M.: 4-Isobutylmethcathinone\u2014A novel synthetic cathinone with high in vitro cytotoxicity and strong receptor binding preference of enantiomers. <em>Pharmaceuticals<\/em> <strong>2022<\/strong>, <em>15<\/em>, 1495.<br><a href=\"https:\/\/doi.org\/10.3390\/ph15121495\">https:\/\/doi.org\/10.3390\/ph15121495<\/a><br><br><\/li>\r\n<li><span _ngcontent-c23=\"\" class=\"authors-text\">Poryvai, A.; \u0160mahel, M.; \u0160vecov\u00e1, M.; Nemati, A.; Shadpour, S.; Ulbrich, P.; Ogolla, T.; Liu, J.; Novotn\u00e1, V.; Veverka, M.; Vejpravov\u00e1 J.; Hegmann, T.; Kohout, M.: Chiral, magnetic, and photosensitive liquid crystalline nanocomposites based on multifunctional nanoparticles and achiral liquid crystals. <em>ACS Nano<\/em>, <strong>2022<\/strong>, <em>16<\/em>, 11833.-11841.<br><\/span><span _ngcontent-c23=\"\" class=\"authors-text\"><a href=\"https:\/\/doi.org\/10.1021\/acsnano.1c10594\" title=\"DOI URL\">https:\/\/doi.org\/10.1021\/acsnano.1c10594<\/a><\/span><span _ngcontent-c23=\"\" class=\"authors-text\"><br><br><\/span><\/li>\r\n<li>Hao, L.; Jing, H.; Xiang, Y.; Iljin, A.; Wang, Y.; Li, H.; Li, Q.; Peng, J.; Kohout, M.: Transient optically induced grating and underlying transport process in bent-core nematics. <em>J. Appl. Phys.<\/em> <strong>2022<\/strong>, <em>132<\/em>, 065108.<br><a href=\"https:\/\/doi.org\/10.1063\/5.0096106\">https:\/\/doi.org\/10.1063\/5.0096106<\/a><br><br><\/li>\r\n<li>Barilone, J. L.; T\u016fma, J.; Brochard, S.; Babkov\u00e1, K.; Krupi\u010dka, M. Design of Bis(1,10-phenanthroline) Copper(I)-Based Mechanochromic Indicators.<em> ACS Omega<\/em> <strong>2022<\/strong>, <em>7<\/em>, 6510-6517.<br><a href=\"https:\/\/doi.org\/10.1021\/acsomega.1c05279\">https:\/\/doi.org\/10.1021\/acsomega.1c05279<\/a> &nbsp;<\/li>\r\n<li>Sysel, P.; Hovorka, \u0160.; Kohout, M.; Holakovsk\u00fd, R.; \u017d\u00e1dn\u00fd, J.; \u010c\u00ed\u017eek, J.; Iz\u00e1k, P. Optically active polyimides with different thermal histories of their preparation. <em>Chirality<\/em><strong> 2022<\/strong>, <em>34<\/em>, 1151-1161.<br><a href=\"https:\/\/doi.org\/10.1002\/chir.23476\" class=\"epub-doi\" aria-label=\"Digital Object Identifier\">https:\/\/doi.org\/10.1002\/chir.23476<\/a><br><br><\/li>\r\n<li>Asnin, L.; Hercikov\u00e1, J.; Lindner, W.; Klimova, Y.; Ziganshina, D.; Reshetova, E.; Kohout, M.: Chiral separation of dipeptides on Cinchona-based zwitterionic chiral stationary phases under buffer-free reversed-phase conditions. <em>Chirality<\/em> <strong>2022<\/strong>, <em>34<\/em>, 1065-1077.<br><a href=\"https:\/\/doi.org\/10.1002\/chir.23471\" class=\"epub-doi\" aria-label=\"Digital Object Identifier\">https:\/\/doi.org\/10.1002\/chir.23471<\/a><br><br><\/li>\r\n<li>Malin\u010d\u00edk, J.; Kohout, M.; Svoboda, J.; Stulov, S.; Pociecha, D.; B\u00f6hmov\u00e1, Z.; Novotn\u00e1, V. Photochromic spiropyran-based liquid crystals. <em>J. Mol. Liq.<\/em> <strong>2022<\/strong>, <em>346<\/em>, 117842.<br><a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2021.117842\" target=\"_blank\" class=\"anchor doi anchor-default anchor-external-link\" title=\"Persistent link using digital object identifier\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\"><span class=\"anchor-text\">https:\/\/doi.org\/10.1016\/j.molliq.2021.117842<\/span><\/a><br><br><\/li>\r\n<li><span _ngcontent-c23=\"\" class=\"authors-text\">Muraveva, V.; Kozm\u00edk, V.; Kohout, M.; Manko, A.; Piryazev, A.; Ivanov, D.; Abramchuk, S.; Cigl, M.; Bobrovsky, A. The smectogenicity as a crucial factor of broadening of the selective light reflection peak in cholesteric photopolymerizable mixtures. <em>Liq. Cryst.<\/em><strong> 2022<\/strong>, <em>49<\/em>, 1459-1465.<br><\/span><span _ngcontent-c23=\"\" class=\"authors-text\"><a href=\"https:\/\/doi.org\/10.1080\/02678292.2022.2041745\">https:\/\/doi.org\/10.1080\/02678292.2022.2041745<\/a><br><br><\/span><\/li>\r\n<li><span _ngcontent-c23=\"\" class=\"authors-text\"><span _ngcontent-c23=\"\" class=\"authors-text\"><span _ngcontent-c23=\"\" class=\"authors-text\">\u0160tefkov\u00e1-Mazochov\u00e1, K.; Danda, H.; Dehaen, W.; Jur\u00e1sek, B.; \u0160\u00edchov\u00e1, K.; Pinterov\u00e1-Leca, N.; Mazoch, V.; Krausov\u00e1, B.H.; Kysilov, B.; Smejkalov\u00e1, T.; Vyklick\u00fd, L.; Kohout, M.; H\u00e1jkov\u00e1, K.; Svozil, D.; Horsley, R.R.; Kucha\u0159, M.; P\u00e1len\u00ed\u010dek, T.: Pharmacokinetic, pharmacodynamic, and behavioural studies of deschloroketamine in Wistar rats. <em>Br. J. Pharmacol. <\/em><strong>2022<\/strong>, <em>179<\/em>, 65-83.<\/span><\/span><\/span>\r\n<div class=\"epub-section\">&nbsp; &nbsp; &nbsp;&nbsp; <a href=\"https:\/\/doi.org\/10.1111\/bph.15680\" class=\"epub-doi\" aria-label=\"Digital Object Identifier\">https:\/\/doi.org\/10.1111\/bph.15680<\/a><\/div>\r\n<span _ngcontent-c23=\"\" class=\"authors-text\"><span _ngcontent-c23=\"\" class=\"authors-text\"><br><\/span><\/span>\r\n<div class=\"epub-section\"><a href=\"https:\/\/doi.org\/10.1111\/bph.15680\" class=\"epub-doi\" aria-label=\"Digital Object Identifier\"><\/a>&nbsp;<\/div>\r\n<span _ngcontent-c23=\"\" class=\"authors-text\"><\/span><\/li>\r\n<\/ol>\r\n<h3><strong>Publications 2021<\/strong><\/h3>\r\n<ol>\r\n<li><span _ngcontent-c23=\"\" class=\"authors-text\">Shruthi, S.; Smahel, M.;<\/span> Kohout, M.;<span _ngcontent-c23=\"\" class=\"authors-text\"><span _ngcontent-c23=\"\" class=\"authors-text\"> Shanker, G.; Hegde, G.: <br>Influence of linking units on the photo responsive studies of azobenzene liquid Crystals: Application in optical storage devices&nbsp;<br><\/span><\/span><em>J. Mol. Liq.<\/em> <strong>2021<\/strong>, <em>339<\/em>, <span _ngcontent-c15=\"\">116744 DOI:<a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2021.116744\" target=\"_blank\" class=\"doi-link\" rel=\"noopener\">10.1016\/j.molliq.2021.116744<\/a><\/span><span _ngcontent-c23=\"\" class=\"authors-text\"><span _ngcontent-c23=\"\" class=\"authors-text\"><br><\/span><\/span><span _ngcontent-c23=\"\" class=\"authors-text\"><br><\/span><\/li>\r\n<li>Skopalov\u00e1 H., Kozm\u00edk V., \u0160mahel M., Svoboda J., Pacherov\u00e1 O., Kohout M. <span>Mesomorphic properties of non-symmetric bent-core liquid crystals with a lateral substituent in the apex position. <em>Liq. Cryst.<\/em> <strong>2021<\/strong>, <em>48<\/em>, 1010-1024<br><\/span><span><a href=\"https:\/\/doi.org\/10.1080\/02678292.2020.1836567\">https:\/\/doi.org\/10.1080\/02678292.2020.1836567<\/a><br><br><\/span><\/li>\r\n<li><span>Cigl M., Hampl F., Svoboda J., Podoliak N., Stulov S., Kohout M., Novotn\u00e1 V. Laterally substituted biphenyl benzoates \u2013 synthesis and mesomorphic properties. <em>Liq. Cryst.<\/em> <strong>2021<\/strong>, <em>48<\/em>, 526-536<br><a href=\"https:\/\/doi.org\/10.1080\/02678292.2020.1794069\">https:\/\/doi.org\/10.1080\/02678292.2020.1794069<\/a><br><br><\/span><\/li>\r\n<li>Sp\u00e1lovsk\u00e1 D., Pa\u0161kan M., Jur\u00e1sek B., Kucha\u0159 M., Kohout M., Setni\u010dka V. Structural spectroscopic study of enantiomerically pure synthetic cathinones and their major metabolites, <em>New J. Chem.<\/em> <strong>2021<\/strong>, <em>45<\/em>, 850.<br><span><a href=\"https:\/\/doi.org\/10.1039\/D0NJ05065B\"> https:\/\/doi.org\/10.1039\/D0NJ05065B<\/a><br><br><\/span><\/li>\r\n<li>Wolrab D., Fr\u00fchauf P., Kolderov\u00e1 N., Kohout M. <span>Strong cation- and zwitterion-exchange-type mixed-mode stationary phases for separation of pharmaceuticals and biogenic amines in different chromatographic modes<\/span>. <em>J. Chromatogr. A<\/em> <strong>2021<\/strong>, <em>1635<\/em>, 461751.<br><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2020.461751\">https:\/\/doi.org\/10.1016\/j.chroma.2020.461751<\/a><br><br><\/li>\r\n<li>&nbsp;J\u00e1gerov\u00e1, D.; \u0160mahel, M.; Poryvai, A.; Mach\u00e1\u010dek, J.; Novotn\u00e1, V.; Kohout, M.: Photosensitive bent-core liquid crystals with laterally substituted azobenzene unit. <em>Crystals<\/em>, <strong>2021<\/strong>, <em>11<\/em>, 1265.<br><a href=\"https:\/\/doi.org\/10.3390\/cryst11101265\">https:\/\/doi.org\/10.3390\/cryst11101265<\/a><br><br><\/li>\r\n<li>Karongo, R.; Ge, M.; Horak, J.; Gross, H.; Kohout, M.; Lindner, W.; L\u00e4mmerhofer, M.: Rapid enantioselective amino acid analysis by ultra-high performance liquid chromatography-mass spectrometry combining 6-aminoquinolyl-<em>N<\/em>-hydroxysuccinimidyl carbamate derivatization with core-shell quinine carbamate anion exchanger separation.<em> J. Chromatogr. Open<\/em>,<strong> 2021<\/strong>, <em>1<\/em>, 100004.<br><a href=\"https:\/\/doi.org\/10.1016\/j.jcoa.2021.100004\" target=\"_blank\" class=\"anchor doi anchor-default anchor-external-link\" title=\"Persistent link using digital object identifier\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\"><span class=\"anchor-text\">https:\/\/doi.org\/10.1016\/j.jcoa.2021.100004<\/span><\/a><br><br><\/li>\r\n<li>Hercikov\u00e1, J.; Sp\u00e1lovsk\u00e1, D.; Fr\u00fchauf, P.; Iz\u00e1k, P.; Lindner, W.; Kohout, M.: Design and synthesis of naphthalene-based chiral strong cations exchangers and their application for chiral separation of basic drugs. <em>J. Sep. Sci., <\/em><strong>2021<\/strong>, <em>44<\/em>, 3348-3356. <span class=\"identifier doi\"><\/span><span class=\"identifier doi\"><span class=\"id-label\"><\/span><span class=\"id-label\">DOI: <\/span> <a href=\"https:\/\/doi.org\/10.1002\/jssc.202100127\" target=\"_blank\" class=\"id-link\" rel=\"noopener\" data-ga-category=\"full_text\" data-ga-action=\"DOI\"> 10.1002\/jssc.202100127 <\/a> <\/span><\/li>\r\n<\/ol>\r\n<p>&nbsp;<\/p>\r\n<h3><strong>Publications 2020<\/strong><\/h3>\r\n<ol>\r\n<li>Poryvai A., Bubnov A., Kohout M. Chiral Photoresponsive Liquid Crystalline Materials Derived from Cyanoazobenzene Central Core: Effect of UV Light Illumination on Mesomorphic Behavior. <em>Crystals<\/em> <strong>2020<\/strong>, <em>10<\/em>, 1161.<br><span><a href=\"https:\/\/doi.org\/10.3390\/cryst10121161\">https:\/\/doi.org\/10.3390\/cryst10121161<\/a><br><br><\/span><\/li>\r\n<li>Tlust\u00fd M., Sp\u00e1lovsk\u00e1 D., Kohout M., Eigner V., Lhot\u00e1k P. Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes. <em>Chem. Commun.<\/em> 2020, <em>56<\/em>, 12773.<br><a href=\"https:\/\/doi.org\/10.1039\/D0CC05352J\">https:\/\/doi.org\/10.1039\/D0CC05352J<\/a><br><br><\/li>\r\n<li>Skopalov\u00e1 H., \u0160pa\u010dek P., Kozm\u00edk V., Svoboda J., Novotn\u00e1 V., Pociecha D., Kohout M. The Role of Substitution in the Apex Position of the Bent-Core on Mesomorphic Properties of New Series of Liquid Crystalline Materials. <em>Crystals<\/em>, <strong>2020<\/strong>, <em>10<\/em>, 735. <span><a href=\"https:\/\/doi.org\/10.3390\/cryst10090735\">https:\/\/doi.org\/10.3390\/cryst10090735<\/a><br><br><\/span><\/li>\r\n<li>Guselnikova O., Postnikov P., Kolsk\u00e1 Z., Z\u00e1ruba K., Kohout M., Elashnikov R., \u0160vor\u010d\u00edk V., Lyutakov O. <span>Homochiral metal-organic frameworks functionalized SERS substrate for atto-molar enantio-selective detection<\/span>. <em>Appl. Mater. Today<\/em> <strong>2020<\/strong>, <em>20<\/em>, 100666.<br><span><a href=\"https:\/\/doi.org\/10.1016\/j.apmt.2020.100666\">https:\/\/doi.org\/10.1016\/j.apmt.2020.100666<\/a><br><br><\/span><\/li>\r\n<li>Kolderov\u00e1 N., Jur\u00e1sek B., Kucha\u0159 M., Lindner W., Kohout M. <span>Gradient supercritical fluid chromatography coupled to mass spectrometry with a gradient flow of make-up solvent for enantioseparation of cathinones<\/span>. <em>J. Chromatogr. A<\/em> <strong>2020<\/strong>, <em>1625<\/em>, 461286. <span><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2020.461286\">https:\/\/doi.org\/10.1016\/j.chroma.2020.461286<\/a><br><br><\/span><\/li>\r\n<li>Tlust\u00fd M., Dvo\u0159\u00e1kov\u00e1 H., \u010cejka J., Kohout M., Lhot\u00e1k P. <span>Regioselective Formation of Quinazoline Moiety on the Upper Rim of Calix[4]arene as the Way to Inherently Chiral Systems<\/span>. <em>New J. Chem.<\/em> <strong>2020<\/strong>, <em>44<\/em>, 6490.<span> <br><a href=\"https:\/\/doi.org\/10.1039\/D0NJ01035A\">https:\/\/doi.org\/10.1039\/D0NJ01035A<\/a><br><br><\/span><\/li>\r\n<li>\u0160mahel M., Poryvai A., Xiang Y., Pociecha D., Troha T., Novotn\u00e1 V., Svoboda J., Kohout M. Photosensitive bent-core nematic liquid crystals with various linking units in the side arms: Structure-properties relationships. <em>J. Mol. Liq.<\/em> <strong>2020<\/strong>, <em>306<\/em>, 112743. <span><a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2020.112743\">https:\/\/doi.org\/10.1016\/j.molliq.2020.112743<\/a><br><br><\/span><\/li>\r\n<li>Cigl M., Jurok R., Hampl F., Svoboda J., Podoliak N., Novotn\u00e1 V.: Lateral substituted phenyl biphenylcarboxylates \u2012 non-chiral analogues of ferroelectric liquid crystals. <em>Liq.&nbsp; Cryst.<\/em> <strong>2020<\/strong>, <em>47<\/em>, 768-776.<br><span><a href=\"https:\/\/doi.org\/10.1080\/02678292.2019.1679903\">https:\/\/doi.org\/10.1080\/02678292.2019.1679903<\/a><br><br><\/span><\/li>\r\n<li>Ga\u00e1lov\u00e1 J., Yalcinkaya F., Cu\u0159\u00ednov\u00e1 P., Kohout M., Yalcinkaya B., Ko\u0161tejn M., Jirs\u00e1k J., Stibor I., Bara J. E., Van der Bruggen B., Iz\u00e1k P. <span>Separation of racemic compound by nanofibrous composite membranes with chiral selector. <em>J. Membr. Sci.<\/em> <strong>2020<\/strong>, <em>596<\/em>, 117728.<br><\/span><span><a href=\"https:\/\/doi.org\/10.1016\/j.memsci.2019.117728\">https:\/\/doi.org\/10.1016\/j.memsci.2019.117728<\/a><br><br><\/span><\/li>\r\n<li><span>Otmar M., Ga\u00e1lov\u00e1 J., \u017ditka J., Bro\u017eov\u00e1 L., Cu\u0159\u00ednov\u00e1 P., Kohout M., Hovorka \u0160., Bara J. E., Van der Bruggen B., Jirs\u00e1k J., Iz\u00e1k P. Preparation of PSEBS membranes bearing (<em>S<\/em>)-(-)-methylbenzylamine as chiral selector. <em>Eur. Polym. J.<\/em> <strong>2020<\/strong>, <em>122<\/em>, 109381. <a href=\"https:\/\/doi.org\/10.1016\/j.eurpolymj.2019.109381\">https:\/\/doi.org\/10.1016\/j.eurpolymj.2019.109381<\/a><\/span><\/li>\r\n<\/ol>\r\n<p>&nbsp;<\/p>\r\n<h3><strong>Publications <\/strong><strong> 2019<\/strong><\/h3>\r\n<ol start=\"9\">\r\n<li>Jing, H.; Xu, M.; Xiang, Y.; Wang, E.; Liu, D.; Poryvai, A.; Kohout, M.; \u00c9ber, N.; Buka, A.: Light tunable gratings based on flexoelectric effect in photoresponsive bent-core nematics. <em>Adv. Opt. Mater.<\/em> <strong>2019<\/strong>, 1801790. <br><a href=\"https:\/\/doi.org\/10.1002\/adom.201801790\">https:\/\/doi.org\/10.1002\/adom.201801790<\/a><br><br><\/li>\r\n<li>Pokluda, A.; Kohout, M.; Chudoba, J.; Krupi\u010dka, M.; Cibulka, R.: Nitrosobenzene: Reagent for the Mitsunobu esterification reaction. <em>ACS Omega<\/em> <strong>2019<\/strong>, <em>4<\/em>, 5012-5018.<br><a href=\"https:\/\/doi.org\/10.1021\/acsomega.8b03551\">https:\/\/doi.org\/10.1021\/acsomega.8b03551<\/a><br><br><\/li>\r\n<li>Sp\u00e1lovsk\u00e1, D.; Ma\u0159\u00edkov\u00e1, T.; Kohout, M.; Kr\u00e1l\u00edk, F.; Kucha\u0159, M.; Setni\u010dka, V.: Methylone and pentylone: Structural analysis of new psychoactive substances. <em>Forensic Toxicol.<\/em> <strong>2019<\/strong>, <em>37<\/em>, 366-377.<br><a href=\"https:\/\/doi.org\/10.1007\/s11419-019-00468-z\">https:\/\/doi.org\/10.1007\/s11419-019-00468-z<\/a><br><br><\/li>\r\n<li>Poryvai, A.; Bubnov, A.; Pociecha, D.; Svoboda, J.; Kohout, M.: The effect of the length of terminal n-alkyl carboxylate chain of self-assembling and photosensitive properties of chiral lactic acid derivatives. <em>J. Mol. Liq.<\/em> <strong>2019<\/strong>, <em>275<\/em>, 829-838.<br><a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2018.11.058\">https:\/\/doi.org\/10.1016\/j.molliq.2018.11.058<\/a><br><br><\/li>\r\n<li>Geibel, C.; Dittrich, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; L\u00e4mmerhofer, M.: Evaluation of superficially porous particle based zwitterionic chiral ion exchangers against fully porous particle benchmarks for enantioselective ultra-high performance liquid chromatography. <em>J. Chromatogr. A<\/em> <strong>2019<\/strong>, <em>1603<\/em>, 130-140.<br><a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2019.06.026\">https:\/\/doi.org\/10.1016\/j.chroma.2019.06.026<\/a><br><br><\/li>\r\n<li>Poryvai, A.; Vojtylov\u00e1-Jurkovi\u010dov\u00e1, T.; \u0160mahel, M.; Kolderov\u00e1, N.; Tom\u00e1\u0161kov\u00e1, P.; S\u00fdkora, D.; Kohout, M.: Determination of optical purity of lactic acid-based chiral liquid crystals and corresponding building blocks by chiral high-performance liquid chromatography and supercritical fluid chromatography. <em>Molecules<\/em> <strong>2019<\/strong>, <em>24<\/em>, 1099.<br><a href=\"https:\/\/dx.doi.org\/10.3390%2Fmolecules24061099\">10.3390\/molecules24061099<\/a><br><br><\/li>\r\n<li>Tlust\u00fd, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhot\u00e1k, P.: Synthesis of upper rim-double-bridged calix[4]arenes bearing seven membered rings and related compounds. <em>RSC Adv.<\/em> <strong>2019<\/strong>, <em>9<\/em>, 22017-22030.<br><a href=\"https:\/\/doi.org\/10.1039\/C9RA05075B\">https:\/\/doi.org\/10.1039\/C9RA05075B<\/a><br><br><\/li>\r\n<li>Hor\u010dic, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: W-shaped mesogens and variations of their molecular structure. <em>Liq. Cryst.<\/em> <strong>2019<\/strong>, <em>46<\/em>, 816-824.<br><a href=\"https:\/\/doi.org\/10.1080\/02678292.2019.1573328\">https:\/\/doi.org\/10.1080\/02678292.2019.1573328<\/a><br><br><\/li>\r\n<li>Cigl, M.; Jurok, R.; Hampl, F.; Svoboda, J.; Podoliak, N.; Novotn\u00e1, V.: Lateral substituted phenyl biphenylcarboxylates \u2013 non-chiral analogues of ferroelectric liquid crystals. Liq. Cryst. 2019. <br><a href=\"https:\/\/doi.org\/10.1080\/02678292.2019.1679903\">https:\/\/doi.org\/10.1080\/02678292.2019.1679903<\/a><br><br><\/li>\r\n<li>Kohout, M.; Hovorka, \u0160.; Hercikov\u00e1, J.; Wilk, M.; Sysel, P.; Iz\u00e1k, P.; Bart\u016fn\u011bk, V.; von Baeckmann, C.; P\u00edcha, J.; Fr\u00fchauf, P.: Evaluation of silica from different vendors as the solid support of anion-exchange chiral stationary phases by means of preferential sorption and liquid chromatography. <em>J. Sep. Sci.<\/em> <strong>2019<\/strong>, <em>42<\/em>, 3653-3661.<br><a href=\"https:\/\/doi.org\/10.1002\/jssc.201900731\">https:\/\/doi.org\/10.1002\/jssc.201900731<\/a><\/li>\r\n<\/ol>\r\n<p>&nbsp;<\/p>\r\n<h3><strong>Publications 2018<\/strong><\/h3>\r\n<ol>\r\n<li>Jur\u00e1sek, B.; Kr\u00e1l\u00edk, F.; Rimpelov\u00e1 S.; \u010cejka, J.; Setni\u010dka, V.; Ruml, T.; Kucha\u0159, M.;&nbsp;Kohout, M.:Synthesis, Absolute Configuration and&nbsp;<em>in vitro<\/em>Cytotoxicity of Deschloroketamine Enantiomers: Rediscovered and Abused Dissociative Anaesthetic<br><em> J. Chem.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>42<\/em>, 19360-19368 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/c8nj03107j\">10.1039\/c8nj03107j<\/a><br><br><\/li>\r\n<li>Landovsky, T.; Dvorakova, H.; Eigner, V.; Babor, M.; Krupicka, M.; Kohout, M.; Lhotak, P.:Chemoselective Oxidation of Phenoxathiin-based Thiacalix[4]arene and the Stereoselective Alkylation of Products<br><em>New J. Chem.<\/em><strong>2018<\/strong>,&nbsp;<em>42<\/em>, 20074-20086 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/C8NJ04690E\">1039\/C8NJ04690E<\/a><br><br><\/li>\r\n<li>Schmitt, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; L\u00e4mmerhofer, M.:<br>Comparison of small size fully porous particles and superficially porous particles of chiral anion-exchange type stationary phases in ultra-high performance liquid chromatography: effect of particle and pore size on chromatographic efficiency and kinetic performance<br><em> Chromatogr. A<\/em><strong>2018<\/strong>,&nbsp;<em>1569<\/em>, 149-159 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.chroma.2018.07.056\">10.1016\/j.chroma.2018.07.056<\/a><br><br><\/li>\r\n<li>&nbsp;Sp\u00e1lovsk\u00e1, D.; Kralik, F.; Kohout, M.; Jurasek, B.; Habartov\u00e1, L.; Kuchar, M.; Setnicka, V.:&nbsp;Structure determination of butylone as a new psychoactive substance using chiroptical and vibrational spectroscopies&nbsp;<br><em>Chirality<\/em><strong>2018<\/strong>,&nbsp;<em>30<\/em>, 548-559 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/chir.22825\">1002\/chir.22825<\/a><br><br><\/li>\r\n<li>Wolrab, D.; Kohout, M.: Multimod\u00e1ln\u00ed stacion\u00e1rn\u00ed f\u00e1ze pro kapalinovou chromatografii, zp\u016fsob jejich p\u0159\u00edpravy a jejich pou\u017eit\u00ed. N\u00e1rodn\u00ed patent \u010d. 307339, \u010d\u00edslo p\u0159ihl\u00e1\u0161ky 2017-193, datum ud\u011blen\u00ed 2.5.2018, datum zve\u0159ejn\u011bn\u00ed 13.6.2018.<br><br><\/li>\r\n<li>Kohout, M.; Wernisch, S.; Tuma, J.; Hettegger, H.; Picha, J.; Lindner W.:&nbsp;Effect of different immobilization strategies on chiral recognition properties of Cinchona-based anion exchangers&nbsp;<br><em> Sep. Sci.<\/em><strong>2018<\/strong>,&nbsp;<em>41<\/em>, 1355-1364 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701213\">10.1002\/jssc.201701213<\/a><br><br><\/li>\r\n<li>Bajtai, A.; Fekete, B.; Palk\u00f3, M.; F\u00fcl\u00f6p, F.; Lindner, W.; Kohout, M.; Ilisz, I.; P\u00e9ter, A.:&nbsp; Comparative study on the liquid chromatographic enantioseparation of cyclic \u03b2-amino acids and the related cyclic \u03b2-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases&nbsp;<br><em> Sep. Sci.<\/em><strong>2018<\/strong>,&nbsp;<em>41<\/em>, 1216-1223 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701190\">10.1002\/jssc.201701190<\/a><br><br><\/li>\r\n<li>Sardella, R.; Macchiarulo, A.; Urbinati, F.; Ianni, F.; Carotti, A.; Kohout, M.; Lindner, W.; P\u00e9ter, A.; Ilisz, I.: Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers&nbsp;<br><em> Sep. Sci.<\/em><strong>2018<\/strong>,&nbsp;<em>41<\/em>, 1199-1207 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701068\">10.1002\/jssc.201701068<\/a><br><br><\/li>\r\n<li>Tuma, J.; Kohout, M.:&nbsp;Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation&nbsp;<br><em>RSC Adv.<\/em><strong>2018<\/strong>,&nbsp;<em>8<\/em>, 1174-1181 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c7ra12658a\">1039\/c7ra12658a<\/a><br><br><\/li>\r\n<li>Kozmik, V.; Rodinov\u00e1, E.; Prausov\u00e1, T.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Mesogens with central naphthalene core substituted at various positions&nbsp;<br>Cryst.&nbsp;<strong>2018<\/strong>, 45, 744-756 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2017.1380238\">10.1080\/02678292.2017.1380238<\/a><br><br><\/li>\r\n<li>Bajz\u00edkov\u00e1, K.; Vesely, J.; Kozmik, V.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Thiophene&nbsp;central core for the design of bent-shaped liquid crystals&nbsp;<br><em> Mol. Liq.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>267<\/em>, 496-503&nbsp;DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.molliq.2018.02.009\">10.1016\/j.molliq.2018.02.009<\/a><br><br><\/li>\r\n<li>Horcic, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.; Gorecka, E.: Bent-core dimers with top-to-bottom linkage between central units&nbsp;<br>RSC Adv.&nbsp;<strong>2018<\/strong>,&nbsp;<em>8<\/em>, 22974-22985 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/c8ra04108c\">1039\/c8ra04108c<\/a><br><br><\/li>\r\n<li>Marz, M.; Kohout, M.; Nevesely, T.;&nbsp;Chudoba, J.; Prukala, D.; Nizinski, S.; Sikorski, M.; Burdzinski, G.;&nbsp;Cibulka, R.:Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control<br><em> Biomol. Chem.<\/em><strong>2018<\/strong>,&nbsp;<em>16<\/em>, 6809-6817 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C8OB01822G\">10.1039\/C8OB01822G<\/a><\/li>\r\n<\/ol>\r\n<p><strong>&nbsp;&nbsp;<\/strong><\/p>\r\n<h3><strong>Publications 2017<\/strong><\/h3>\r\n<ol start=\"4\">\r\n<li>Maixner, J.; Jur\u00e1sek, B.; Kohout, M.; Kuchar, M.; Kacer, P.: X-ray powder diffraction data for (S)-Deschloroketamine hydrochloride, C<sub>13<\/sub>H<sub>18<\/sub> <em>Powder Diffr.<\/em><strong>2017<\/strong>,&nbsp;<em>32<\/em>, 193-195. DOI:<a href=\"http:\/\/dx.doi.org\/10.1017\/S0885715617000586\">10.1017\/S0885715617000586<\/a><br><br><\/li>\r\n<li>Bajz\u00edkov\u00e1, K.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.; Gorecka E.: Bent-core mesogens with an aromatic unit at the terminal position. <em>New J. Chem.<\/em><strong>2017<\/strong>,&nbsp;<em>41<\/em>,&nbsp;4672-4679 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/C6NJ03908A\">1039\/C6NJ03908A<\/a><br><br><\/li>\r\n<li>\u017durek, J.; Svobodov\u00e1, E.; \u0160turala, J.; Dvo\u0159\u00e1kov\u00e1, H.;Svoboda, J.; Cibulka, R.: Chiral ethylene-bridged flavinium salts: The stereoselectivity of flavin-10a-hydroperoxide formation and the effect of substitution on the photochemical properties. <em>Tetrahedron Asymmetry<\/em>&nbsp;<strong>2017<\/strong>, 28, 1780-1791. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetasy.2017.10.029\">1016\/j.tetasy.2017.10.029<\/a><br><br><\/li>\r\n<li>Dobrovolny, K.; Ulbrich, P.; Svecova, M.; Rimpelova, S.;&nbsp;Malincik, J.;&nbsp;Kohout, M.; Svoboda, J.; Bartunek, V.:&nbsp;Copper nanoparticles in glycerol-\u200bpolyvinyl alcohol matrix: In situ preparation, stabilization and antimicrobial aktivity. <em> Alloy. Compd.<\/em><strong>2017<\/strong>,<em>&nbsp;697<\/em>, 147-155 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jallcom.2016.12.144\">10.1016\/j.jallcom.2016.12.144<\/a><br><br><\/li>\r\n<li>Kolderova, N.;&nbsp;Nevesely, T.; Sturala, J.; Kuchar, M.;&nbsp;Holakovsky, R.;&nbsp;Kohout, M.:<br>Enantioseparation of chiral sulfoxides on amylose-\u200bbased columns: comparison of normal phase liquid chromatography and supercritical fluid chromatography <em>Chromatographia<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>80<\/em>, 547-557 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1007\/s10337-016-3234-6\">10.1007\/s10337-016-3234-6<\/a><br><br><\/li>\r\n<li>Kohout, M.; Alaasar, M.;&nbsp;Poryvai, A.; Novotna, V.; Poppe, S.; Tschierske, C.;&nbsp;Svoboda, J.: Photosensitive bent-\u200bcore liquid crystals based on methyl substituted 3-\u200bhydroxybenzoic acid<br><em>RSC Adv.<\/em><strong>2017<\/strong>,&nbsp;<em>7<\/em>, 35805-35813 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7RA05632J\">10.1039\/C7RA05632J<\/a><br><br><\/li>\r\n<li>Wolrab, D.; Fruehauf, P.; Gerner, C.;&nbsp;Kohout, M.;Lindner, W.: Consequences of transition from liquid chromatography to supercritical fluid chromatography on the overal performance of a chiral zwitterionic ion-\u200bexchanger. <em>J. Chromatogr. A<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>1517<\/em>, 165-175 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.chroma.2017.08.022\">10.1016\/j.chroma.2017.08.022<\/a><br><br><\/li>\r\n<li>Pallova, L.;Kozmik, V.; Kohout, M.; Svoboda, J.;&nbsp;Novotna, V.; Pociecha, D.:&nbsp;Bent-\u200bcore liquid crystals with a 2-\u200bsubstituted 3-\u200bhydroxybenzoic acid central core. <em> Cryst.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>44<\/em>, 1306-1315 DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1276981\">10.1080\/02678292.2016.1276981<\/a><br><br><\/li>\r\n<li>Tlusty, M.; Slavik, P.; Kohout, M.; Eigner, V.; Lhotak, P.: Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring<br><em>Org. Lett.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>19<\/em>, 2933-2936 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b01170\">10.1021\/acs.orglett.7b01170<\/a><br><br><\/li>\r\n<li>Miksatko, J.; Eigner, V.;&nbsp;Kohout, M.; Lhotak, P.: Regio-\/stereoselective Formation of Monosulfoxides from Thiacalix[4]arenes in All Possible Conformations<br><em>Tetrahedron Letters<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>58<\/em>, 1687\u20131691 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2017.03.043\">10.1016\/j.tetlet.2017.03.043<\/a><br><br><\/li>\r\n<li>Hor\u010dic, M.; Kohout, M.;&nbsp;Svoboda, J.;&nbsp;Novotna, V.; Pociecha, D.; Gorecka, E.: Core-to-core Dimers Forming Switchable Mesophase<br><em>Chem. &nbsp;Commun.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>53<\/em>, 2721-2724 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6CC09983A\">10.1039\/C6CC09983A<\/a><br><br><\/li>\r\n<li>M\u00e4rz, M.;&nbsp;Chudoba, J.;&nbsp;Kohout, M.;&nbsp;Cibulka, R.: Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light<br><em>Org. Biomol. Chem.&nbsp;<\/em><strong>2017<\/strong><em>, 15,&nbsp;<\/em>1970-1975&nbsp;DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6OB02770A\">10.1039\/C6OB02770A<\/a><\/li>\r\n<\/ol>\r\n<h3><strong>&nbsp;<\/strong><\/h3>\r\n<h3><strong>Publications 2016<\/strong><\/h3>\r\n<ol>\r\n<li>Bajzikova, K.; Kohout, M.; Tarabek, J.; Svoboda, J.; Novotna, V.; Vejpravova, J.; Pociecha, D.; Gorecka, E.: All-organic liquid crystalline radicals with a spin unit in the outer position of a bent-core syst\u00e9m. <em>J. Mater. Chem. C<\/em><strong>2016<\/strong>,&nbsp;<em>4<\/em>, 11540-11547.&nbsp; DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6TC04346A\">10.1039\/C6TC04346A<\/a><br><br><\/li>\r\n<li>T\u016fma, J.; Kohout, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Bent-core liquid crystals based on 6-substituted 3-hydroxybenzoic acid: the role of substitution and linkage group orientation on mesomorphic properties. <em>Liq. Cryst.<\/em><strong>2016<\/strong>,&nbsp;<em>43<\/em>, 1889-1900.&nbsp; DOI:<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1230789\">10.1080\/02678292.2016.1230789<\/a><br><br><\/li>\r\n<li>Kohout, M.; Vandenbussche, J.; Roller, A.; T\u016fma, J.; Boqaerts, J.; Bultinck, P.; Herrebout, W.; Lindner, W.: Absolute configuration of the antimalarial&nbsp;<em>erythro<\/em>-mefloquine - vibrational dichroism and X-ray diffraction studies of mefloquine and its thiourea derivative. <em>RSC Advances<\/em><strong>2016<\/strong>,&nbsp;<em>6<\/em>, 81461-81465. DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6RA19367F\">1039\/C6RA19367F<\/a>&nbsp;<br><br><\/li>\r\n<li>Kohout, M.; Bubnov, A.; \u0160\u0165urala, J.; Novotn\u00e1, V.; Svoboda, J.: Effect on alkyl chain length in the terminal ester group on mesomorphic properties of new chiral lactic acid derivatives. <em> Cryst.<\/em><strong>2016<\/strong>,&nbsp;<em>43<\/em>,&nbsp;1472-1485. DOI:<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1185170\">10.1080\/02678292.2016.1185170<\/a><br><br><\/li>\r\n<li>Grecs\u00f3, N.; Kohout, M.; Carotti, A.; Sardella, R.; Natalini, B.; F\u00fcl\u00f6p, F.; Lindner, W.; P\u00e9ter, A.; Ilisz, I.:&nbsp;Mechanistic considerations of enantiorecognition on novel <em>Cinchona<\/em> alkaloid-based zwitterionic chiral stationary phases from the aspect of the separation of trans-paroxetine enantiomers as model compounds. <em> Pharm. Biomed. Anal.<\/em><strong>2016<\/strong>,&nbsp;<em>124<\/em>,&nbsp;164-173. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jpba.2016.02.043\">10.1016\/j.jpba.2016.02.043<\/a><br><br><\/li>\r\n<li>Wolrab, D.; Fr\u00fchauf, P.; Moulisova, A.; Kuchar, M.; Gerner, C.; Lindner, W.; Kohout, M.: Chiral separation of new designer drugs (Cathinones) on chiral ion-exchange type stationary phases. <em> Pharm. Biomed. Anal.<\/em><strong>2016<\/strong>,&nbsp;<em>120<\/em>, 306-315. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jpba.2015.12.023\">10.1016\/j.jpba.2015.12.023<\/a><br><br><\/li>\r\n<li>T\u016fma, J.; Kohout, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core - Part II.&nbsp;<em> Cryst.<\/em> <strong>2016<\/strong>,&nbsp;<em>43<\/em>, 547-563&nbsp;DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2015.1125535\">10.1080\/02678292.2015.1125535<\/a><br><br><\/li>\r\n<li>Slavik, P.; Kohout, M.; B\u00f6hm, S.; Eigner, V.; Lhotak, P.: Synthesis of&nbsp;Inherently Chiral Calixarenes via Direct Mercuration of the Partial Cone Conformation.&nbsp;<em>Chem. Comm.<\/em>&nbsp; <strong>2016<\/strong>,&nbsp;<em>52<\/em>, 2366-2360&nbsp;DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5CC09388K\">10.1039\/C5CC09388K<\/a><\/li>\r\n<\/ol>\r\n<p>&nbsp;<\/p>\r\n<h3><strong>Publications 2015<\/strong><\/h3>\r\n<ol start=\"5\">\r\n<li>Tri\u0161ovi\u0107, N.; Antanasijevi\u0107, J.; T\u00f3th-Katona, T.; Kohout, M.; Salamonczyk, M.; Sprunt, S.; J\u00e1kli, A.; Fodor-Csorba, K.: Azo-containing asymmetric bent-core liquid crystals with modulated smectic phase <em>RSC Adv.<\/em> <strong>2015<\/strong>, <em>5<\/em>, 64886-64891. DOI: 10.1039\/c5ra09764a<br><br><\/li>\r\n<li>Kohout, M.; Bielec, B.; Steindl, P.; Trettenhahn, G.; Lindner, W.: Mechanistic aspects of the direct C-acylation of cyclic 1,3-diones with various unactivated carboxylic acids <em>Tetrahedron<\/em> <strong>2015<\/strong>, <em>71<\/em>, 2698-2707. DOI: tet.2015.03.037<br><br><\/li>\r\n<li>von Koschitzky, I.; Gerhardt, H.; L\u00e4mmerhofer, M.; Kohout, M.; Gehringer, M.; Laufer, S.; Pink, M.; Schmitz-Spanke, S.; Strube, C.; Kaiser, A.: New insights into novel inhibitors against deoxyhypusine hydrolase from plasmodium falciparum: compounds with an iron chelating potential <em>Amino Acids<\/em> <strong>2015<\/strong>, <em>47<\/em>, 1155-1166. DOI: 1007\/s00726-015-1943-z<br><br><\/li>\r\n<li>Kohout, M.; Kozm\u00edk, V.; Slabochov\u00e1, M.; T\u016fma, J.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core <em> Cryst.<\/em> <strong>2015<\/strong>, <em>42<\/em>, 87-103. DOI: 10.1080\/02678292.2014.965232<br><br><\/li>\r\n<li>Kozm\u00edk, V.; Poznik, M.; Svoboda, J.; Frere, P.:<br>Dithieno[3,2-b:2',3'-d]furan as a new building block for fused conjugated systems<br><em>Tetrahedron Lett.<\/em><strong>2015<\/strong>,&nbsp;<em>56<\/em>, 6251-6253.&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.09.107\">DOI:10.1016\/j.tetlet.2015.09.107<\/a><\/li>\r\n<\/ol>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["142466"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"142466":{"idvazba":"175468","nad_uzel":"136562","pod_uzel":"142466","url":"","sablona":"4","nazev":"infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"14.07.2026 12:18:00","platne_do":null,"iduzel":"142466","obsah":"a:8:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:5:\"false\";s:12:\"poddokumenty\";s:5:\"false\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:299:\"<ul>\r\n<li><a href=\"\/research\/kohout\" rel=\"follow\">Home<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/people\" rel=\"follow\">People<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/research\" rel=\"follow\">Research<\/a><\/li>\r\n<li><a href=\"\/research\/kohout\/publications\" rel=\"follow\">Publications<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136566":{"idvazba":"167929","nad_uzel":"116995","pod_uzel":"136566","url":"\/research\/krupicka","sablona":"58","nazev":"Group of mechanochemistry and computational chemistry","_url_prefix":"{\/\/uoch.vscht.cz\/research\/krupicka}","poradi":"6","skupina_www":"everyone","platne_od":"08.06.2026 21:02:00","platne_do":null,"iduzel":"136566","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:53:\"Group of mechanochemistry and computational chemistry\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:1510:\"<h1>Group of&nbsp;<span style=\"font-style: normal;\">mechanochemistry <\/span><span style=\"font-style: normal;\">and <\/span>quantum chemistry&nbsp;<\/h1>\r\n<p><strong>Research topic:<br><\/strong>- Application of quantum mechanical methods for prediction of properties of designed molecules<br>- Calculation of spectroscopic properties<br>- Design and optimization of molecular structures for mechanochemical applications<br>- Synthesis of mechanically sensitive compounds<br>- Solid state reactivity using ball mills<\/p>\r\n<p>&nbsp;<img src=\"\/files\/uzel\/0136566\/0002~~S61IBgA.jpg\" class=\"\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"exc (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"330\"><\/p>\r\n<p><strong>We are looking for:<br><\/strong>- Bachelor and master students of organic chemistry<br>- Fans of computational chemistry, programmers or AI afficioinados<br>&nbsp;\u2026 with good grades and interests in lab work (starting at first year)<\/p>\r\n<p>&nbsp;<\/p>\r\n<p><strong>We offer:<br><\/strong>- Working atmosphere and support for writing bachelor and master theses<br>- Interesting projects<br>- In-depth experience of quantum chemical methods and practical skills through research participation<br>- International collaboration including stays abroad<br>- Presentation of results on international meetings<\/p>\r\n<p><img src=\"\/files\/uzel\/0136566\/0001~~KynKSMzLBAA.jpg\" class=\"\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"trhani (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"330\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["139170","136567","136568","136569"],"poduzly_count":4,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":0,"139170":{"idvazba":"171138","nad_uzel":"136567","pod_uzel":"139170","url":"","sablona":"4","nazev":"Infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"07.06.2026 22:07:00","platne_do":null,"iduzel":"139170","obsah":"a:7:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:4:\"true\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:0:\"\";}","class":"infobox","autonomni":"0","pod_uzly":["139171","139171"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"139171":{"idvazba":"171136","nad_uzel":"139170","pod_uzel":"139171","url":"","sablona":null,"nazev":"Home","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"07.06.2026 21:42:00","platne_do":null,"iduzel":"139171","obsah":"a:4:{s:4:\"akce\";s:4:\"Home\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:18:\"\/research\/krupicka\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0}}},"136567":{"idvazba":"171139","nad_uzel":"136566","pod_uzel":"136567","url":"\/research\/krupicka\/people","sablona":"58","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/krupicka\/people}","poradi":"1","skupina_www":"everyone","platne_od":"08.06.2026 21:03:00","platne_do":null,"iduzel":"136567","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:751:\"<h2>Staff<\/h2>\r\n<ul>\r\n<li>Ing. Martin Krupi\u010dka, PhD. (Group leader)<\/li>\r\n<li>Kv\u011bta B\u00e1rtov\u00e1 (Lab Technician)<\/li>\r\n<\/ul>\r\n<h2>Students<\/h2>\r\n<ul>\r\n<li>Bc. Magdalena Pre\u010dov\u00e1<\/li>\r\n<li>Filip Frkal<\/li>\r\n<li>Sofia Mal\u00edkov\u00e1<\/li>\r\n<\/ul>\r\n<h2>Alumni and Guests<\/h2>\r\n<ul>\r\n<li>Ing. Lucie Hlav\u00e1\u010dkov\u00e1 (2026)<\/li>\r\n<li>Ing. Tereza \u0160indel\u00e1\u0159ov\u00e1 (2025)<\/li>\r\n<li>Bc. Patrik F\u00e1brik (2025)<\/li>\r\n<li>Bc. Marek Opelka (2025)<\/li>\r\n<li>Bc. Jakub \u0160ir\u016f\u010dek (2021)<\/li>\r\n<li>Bc. Bohumil Kubi\u0161 (2021)<\/li>\r\n<li>Bc. Lucie Tu\u010dkov\u00e1 (2021)<\/li>\r\n<li>Ing. Kate\u0159ina Babkov\u00e1 (2021)<\/li>\r\n<li>Bc. Veronika \u0160ofrov\u00e1 (2020)<\/li>\r\n<li>Ing. Tatiana Nemirovich (2020)<\/li>\r\n<li>Ing. Lucie R\u00e1zkov\u00e1 (2020)<\/li>\r\n<li>Ing. Marco Vitek (2019)<\/li>\r\n<\/ul>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["139170"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"139170":{"idvazba":"171138","nad_uzel":"136567","pod_uzel":"139170","url":"","sablona":"4","nazev":"Infobox","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"07.06.2026 22:07:00","platne_do":null,"iduzel":"139170","obsah":"a:7:{s:5:\"nazev\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";s:8:\"uslideru\";s:4:\"true\";s:10:\"podstranky\";s:4:\"true\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:0:\"\";}","class":"infobox","autonomni":"0","pod_uzly":["139171","139171"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"139171":{"idvazba":"171136","nad_uzel":"139170","pod_uzel":"139171","url":"","sablona":null,"nazev":"Home","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"07.06.2026 21:42:00","platne_do":null,"iduzel":"139171","obsah":"a:4:{s:4:\"akce\";s:4:\"Home\";s:6:\"objekt\";s:0:\"\";s:5:\"odkaz\";s:18:\"\/research\/krupicka\";s:10:\"idattribut\";s:0:\"\";}","class":null,"autonomni":null,"poduzly_count":0,"poduzly_count_aut":0}}}}},"136568":{"idvazba":"167922","nad_uzel":"136566","pod_uzel":"136568","url":"\/research\/krupicka\/publications_clone_16941","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/krupicka\/publications_clone_16941}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 10:37:28.14929","platne_do":null,"iduzel":"136568","obsah":"a:6:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136569":{"idvazba":"167923","nad_uzel":"136566","pod_uzel":"136569","url":"\/research\/krupicka\/research","sablona":"58","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/krupicka\/research}","poradi":"3","skupina_www":"everyone","platne_od":"08.06.2026 21:03:00","platne_do":null,"iduzel":"136569","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"136600":{"idvazba":"168057","nad_uzel":"116995","pod_uzel":"136600","url":"\/research\/kvicala","sablona":"49","nazev":"Kv\u00ed\u010dala","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala}","poradi":"7","skupina_www":"everyone","platne_od":"03.06.2026 14:18:00","platne_do":null,"iduzel":"136600","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:9:\"Kv\u00ed\u010dala\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:30:\"0006~~S0rMy0stinf1i89LLQcA.png\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:2213:\"<h2 style=\"text-align: center;\"><img src=\"\/images\/0!215\/uzel\/0136600\/0006~~S0rMy0stinf1i89LLQcA.png\" class=\"img_fancy_no\" alt=\" \u25f3 banner_EN_new (png) \u2192 (v\u00fd\u0161ka 215px)\" width=\"946\" height=\"215\">WELCOME TO THE GROUP OF ORGANOFLUORINE CHEMISTRY<\/h2>\r\n<p><strong><span><\/span><\/strong><\/p>\r\n<p><strong><span><img src=\"\/files\/uzel\/0136600\/0003~~c8svyY_PyM9NBQA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Foto_home (jpg) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"292\"><br>WE ARE LOOKING FOR Bc., M.Sc. and Ph.D. STUDENTS<\/span><\/strong><\/p>\r\n<p><strong><span>We offer:<\/span><\/strong><\/p>\r\n<ul>\r\n<li>interesting projects focused mainly on fluorinated organic compounds<\/li>\r\n<li>practical knowledge of organic synthesis<\/li>\r\n<li>international collaboration with the possibility of an internship abroad<\/li>\r\n<li>presentation of results at national and international conferences<\/li>\r\n<li>introduction to computational and visualization methods for theoretical studies<\/li>\r\n<li>friendly atmosphere<\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<br><span>Our latest achievements<\/span><span>:<\/span><\/strong><\/p>\r\n<p><span>Three of our students were successfull at Student<\/span>\u2019s<span> Scientific Conference 20230 organized by UCT Prague. V\u00edt Jen\u00ed\u010dek placed first, Adam Hroch placed second&nbsp; and Kry\u0161tof Malyh placed second in their sessions.<\/span><\/p>\r\n<p><span>Two of our students were successfull at Student\u2019s Scientific Conference 2022 organized by UCT Prague. Michal Trojan placed first and Adam Hroch placed third in their sessions.<\/span><\/p>\r\n<p><strong><span><br>Our latest publications:<\/span><\/strong><\/p>\r\n<p><strong><span>&nbsp;<\/span><\/strong><\/p>\r\n<p><strong><span><img src=\"\/files\/uzel\/0136600\/0004~~8y9Kd8rMz83Pcc5IzY03MjAyAQA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 OrgBiomolChem_2024 (png) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"281\"><br><\/span><\/strong><\/p>\r\n<hr>\r\n<p><\/p>\r\n<p><strong><span><img src=\"\/files\/uzel\/0136600\/0005~~c85IzXUtLfKKNzIwMgYA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 ChemEurJ_2023 (png) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"281\">&nbsp;<\/span><\/strong><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["136601","38652","136604","136608","136609"],"poduzly_count":5,"poduzly_count_aut":4,"poduzly":{"poduzly_count_aut_sum":3,"136601":{"idvazba":"167972","nad_uzel":"136600","pod_uzel":"136601","url":"\/research\/kvicala\/funds_clone_62766","sablona":"1","nazev":"Funds","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/funds_clone_62766}","poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.194348","platne_do":null,"iduzel":"136601","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:5:\"Funds\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:534:\"<h2><strong>Financial support<\/strong><\/h2>\r\n<h3><strong><br \/>Current grant projects:<\/strong><\/h3>\r\n<p>\u201eAdvanced reagents for (asymmetric) nucleophilic fluorination.\u201c (GA CR, 2021-2023)<\/p>\r\n<h3>Cooperation:<\/h3>\r\n<p>Grant project EXPRO: \u201eNanocrystallography of molecular crystals\u201c (GA CR, 2021-2025)<\/p>\r\n<p style=\"text-align: justify;\">European Regional development Fund-Project \"Organic redox couple based batteries for energetics of traditional and renewable resources (ORGBAT)\" No.CZ.02.1.01\/0.0\/0.0\/16_025\/0007445.<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38652"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38652":{"idvazba":"167974","nad_uzel":"136600","pod_uzel":"38652","url":"","sablona":"4","nazev":"Kvicala's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.03.2021 10:26:00","platne_do":null,"iduzel":"38652","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"38652":{"idvazba":"167974","nad_uzel":"136600","pod_uzel":"38652","url":"","sablona":"4","nazev":"Kvicala's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.03.2021 10:26:00","platne_do":null,"iduzel":"38652","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136604":{"idvazba":"167977","nad_uzel":"136600","pod_uzel":"136604","url":"\/research\/kvicala\/people_clone_68561","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/people_clone_68561}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.222963","platne_do":null,"iduzel":"136604","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1870:\"<h3 style=\"text-align: center;\"><strong>Group members:<\/strong><\/h3>\r\n<p><img src=\"\/images\/450!0\/uzel\/0038640\/0004~~c8svyY_PyUw5vBIA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Foto_lid\u00e9 (jpg) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"265\"><\/p>\r\n<p><\/p>\r\n<div id=\"zamestnanci\" style=\"padding-left: 60px;\">&nbsp;&nbsp;&nbsp;\r\n<table style=\"height: 337px; margin-left: auto; margin-right: auto;\" width=\"593\">\r\n<tbody>\r\n<tr>\r\n<td style=\"text-align: left; vertical-align: top;\">\r\n<h3><strong>Employees<br><br><\/strong><\/h3>\r\n<p><a href=\"https:\/\/uoch.vscht.cz\/research-groups\/kvicala-en\/people\/kvicala\" rel=\"follow\">Prof. Ing. Jaroslav Kv\u00ed\u010dala, CSc.<\/a><\/p>\r\n<p>&nbsp;<\/p>\r\n<p><a href=\"https:\/\/uoch.vscht.cz\/research-groups\/kvicala-en\/people\/rybackova\" rel=\"follow\">Ing. Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1, Ph.D.<\/a><\/p>\r\n<p>&nbsp;<\/p>\r\n<p><a href=\"https:\/\/uoch.vscht.cz\/research-groups\/kvicala-en\/people\/stenglova\" rel=\"follow\">Helena \u0160tenglov\u00e1<\/a><\/p>\r\n<br>\r\n<h3><strong><br>Ph.D. students<br><br><\/strong><\/h3>\r\n<p>&nbsp;<\/p>\r\n<p><a href=\"\/vedecke-skupiny\/kvicala\/lide\/lipovska\">Ing. Pavl\u00edna Dund\u00e1lkov\u00e1<\/a><br><br><a href=\"\/vedecke-skupiny\/kvicala\/lide\/kucnirova\" rel=\"follow\">Ing. Kate\u0159ina Ku\u010dnirov\u00e1<\/a><br><br>Bc. \u0160\u00e1rka Bouzkov\u00e1<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<td style=\"text-align: left; vertical-align: top;\">\r\n<h3><strong>Students<br><br><\/strong><\/h3>\r\n<p><\/p>\r\n<p>Bc. V\u00edt Jen\u00ed\u010dek&nbsp;<br><br><\/p>\r\n<p>Bc. Adam Hroch<br><br><\/p>\r\n<p>Bc. \u0160\u00e1rka Pol\u00edvkov\u00e1<br><br><\/p>\r\n<p>Bc. S\u00e1mer Melhem<\/p>\r\n<p><br><span>Bc. Ond\u0159ej Je\u017eowicz<\/span><br><br><\/p>\r\n<p><span>Bc. Kry\u0161tof Mal\u00fd<\/span><br><br><\/p>\r\n<p><span>Jan Mikul\u00e1\u0161t\u00edk<\/span><br><br><\/p>\r\n<p><span>Nadiia Silina<\/span><br><br><\/p>\r\n<p><span>Jakub Krebs<\/span><\/p>\r\n<p><span><\/span><\/p>\r\n<p><span><br>Martina W\u00e1gnerov\u00e1<br><br><\/span><\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38652","136605","136606","136607"],"poduzly_count":4,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":0,"38652":{"idvazba":"167974","nad_uzel":"136600","pod_uzel":"38652","url":"","sablona":"4","nazev":"Kvicala's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.03.2021 10:26:00","platne_do":null,"iduzel":"38652","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136605":{"idvazba":"167979","nad_uzel":"136604","pod_uzel":"136605","url":"\/research\/kvicala\/people_clone_68561\/stenglova_clone_42733","sablona":"1","nazev":"Helena \u0160tenglov\u00e1","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/people_clone_68561\/stenglova_clone_42733}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.30195","platne_do":null,"iduzel":"136605","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:18:\"Helena \u0160tenglov\u00e1\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:502:\"<p><strong><img src=\"\/images\/215!0\/uzel\/0058103\/0001~~80jNSc1LBAA.jpg\" class=\"img_float_left img_fancy_no\" alt=\" \u25f3 Helena\" width=\"215\" height=\"277\" \/>Helena \u0160tenglov\u00e1<\/strong><\/p>\r\n<p><span>&nbsp;<\/span><span>Technician<\/span><\/p>\r\n<p><span>&nbsp;<\/span><span>Department of Organic Chemistry<br \/>University of Chemistry and Technology, Prague<br \/>Technick\u00e1 5<br \/>166 28 Prague 6<br \/>tel: +420 220 444 242<br \/>e-mail: Helena.Stenglova<\/span>@vscht.cz<span><br \/>building A, room 259<\/span><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136606":{"idvazba":"167980","nad_uzel":"136604","pod_uzel":"136606","url":"\/research\/kvicala\/people_clone_68561\/rybackova_clone_85152","sablona":"1","nazev":"Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/people_clone_68561\/rybackova_clone_85152}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.322045","platne_do":null,"iduzel":"136606","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:21:\"Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1484:\"<p><strong><img src=\"\/images\/215!0\/uzel\/0058102\/0001~~800syk4tSQQA.jpg\" class=\"img_float_left img_fancy_no\" alt=\" \u25f3 Marketa\" width=\"215\" height=\"277\" \/>Ing. Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1, Ph.D.<\/strong><\/p>\r\n<p><span>&nbsp;<\/span><span>Assistant Professor<\/span><\/p>\r\n<p><span>&nbsp;<\/span><span>Department of Organic Chemistry<br \/>University of Chemistry and Technology, Prague<br \/>Technick\u00e1 5<br \/>166 28 Prague 6<br \/>tel: +420 220 444 242<br \/>e-mail: Marketa.Rybackova<\/span>@vscht.cz<span><br \/>building A, room 259<\/span><\/p>\r\n<p><span>&nbsp;<br \/><br \/><br \/><br \/><br \/><br \/><br \/><\/span><\/p>\r\n<h3>Education<\/h3>\r\n<ul>\r\n<li><strong>1998-2003 <\/strong>master degree at UCT Prague<\/li>\r\n<li><strong>2003-2007 <\/strong>doctoral degree at UCT Prague\/IOCB Prague<\/li>\r\n<\/ul>\r\n<h3><strong>&nbsp;<\/strong>Experience<\/h3>\r\n<ul>\r\n<li><strong>01-07\/2006 <\/strong>Erasmus internship at University of Copenhagen (prof. Nielsen group)<\/li>\r\n<li>since&nbsp;<strong>2007 <\/strong>member of Organofluorine chemistry group<\/li>\r\n<li>since&nbsp;<strong>2008 <\/strong>assistant professor at Department of Organic Chemistry, UCT Prague<\/li>\r\n<\/ul>\r\n<p><span>&nbsp;<\/span><\/p>\r\n<h3>Courses overview<\/h3>\r\n<ul>\r\n<li>Organic Chemistry I, II, A &amp;B (seminars)<\/li>\r\n<li>Organic Chemistry: Laboratory I &amp; II<\/li>\r\n<li>Specialized Laboratory \u2013 Organic Chemistry<\/li>\r\n<li>Laboratory of Specialization Synthesis of Drugs<\/li>\r\n<\/ul>\r\n<p><span>&nbsp;<\/span><\/p>\r\n<p><u><span>&nbsp;<\/span><\/u><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136607":{"idvazba":"167981","nad_uzel":"136604","pod_uzel":"136607","url":"\/research\/kvicala\/people_clone_68561\/kvicala_clone_72073","sablona":"1","nazev":"Jaroslav Kv\u00ed\u010dala","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/people_clone_68561\/kvicala_clone_72073}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.331287","platne_do":null,"iduzel":"136607","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:18:\"Jaroslav Kv\u00ed\u010dala\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1808:\"<p><strong><img src=\"\/images\/215!0\/uzel\/0058101\/0001~~8woEAA.jpg\" class=\"img_float_left img_fancy_no\" alt=\" \u25f3 JQ (jpg)\" width=\"215\" height=\"262\" \/>Prof. Ing. Jaroslav Kv\u00ed\u010dala, CSc.<\/strong><\/p>\r\n<p><span>&nbsp;<\/span><span>Head of the research group<\/span><\/p>\r\n<p><span>&nbsp;<\/span><span>Department of Organic Chemistry<br \/>University of Chemistry and Technology, Prague<br \/>Technick\u00e1 5<br \/>166 28 Prague 6<br \/>tel: +420 220 444 240<br \/>e-mail: Jaroslav.Kvicala<\/span>@vscht.cz<span><br \/>building A, room 278d<br \/><br \/><br \/><br \/><br \/><br \/><br \/><\/span><\/p>\r\n<h3>Education<\/h3>\r\n<ul>\r\n<li><strong>1975-1980<\/strong>master degree at UCT Prague<\/li>\r\n<li><strong>1980-1987<\/strong>doctoral degree at UCT Prague<\/li>\r\n<\/ul>\r\n<p>&nbsp;<\/p>\r\n<h3>&nbsp;Experience<\/h3>\r\n<p>&nbsp;<\/p>\r\n<ul>\r\n<li><strong>1984-1986 <\/strong>Scientist at V\u00daAnCh \u00dast\u00ed n. L.<\/li>\r\n<li><strong>1986-1988 <\/strong>Scientist at the Department of Organic Chemistry, UCT Prague<\/li>\r\n<li><strong>1988-2006 <\/strong>Assistant Professor at the Department of Organic Chemistry, UCT Prague<\/li>\r\n<li><strong>1992 <\/strong>ENSCM Montpellier<\/li>\r\n<li><strong>1993-1994, 1995<\/strong> Swansea University of Wales<\/li>\r\n<li><strong>2003-2004 <\/strong>University of Colorado at Boulder (prof. Michl group)<\/li>\r\n<li>since&nbsp;<strong>2006 <\/strong>Associate Professor at the Department of Organic Chemistry, UCT Prague<\/li>\r\n<li>since&nbsp;<strong>2015 <\/strong>Full Professor at the Department of Organic Chemistry, UCT Prague<\/li>\r\n<\/ul>\r\n<p>&nbsp;<\/p>\r\n<h3>Courses overview<\/h3>\r\n<ul>\r\n<li>Organic Chemistry I, II, A &amp; B<\/li>\r\n<li>Organic Chemistry: Laboratory I &amp; II<\/li>\r\n<li>Computations and Visualization of Molecules<\/li>\r\n<li>Organic Chemistry of Selected Elements<\/li>\r\n<\/ul>\r\n<p><span><br \/><br \/><\/span><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"136608":{"idvazba":"167982","nad_uzel":"136600","pod_uzel":"136608","url":"\/research\/kvicala\/research_clone_16760","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/research_clone_16760}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.340755","platne_do":null,"iduzel":"136608","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1553:\"<h2><strong>Current topics studied in our group:<br \/><br \/><\/strong><\/h2>\r\n<ul>\r\n<li><strong><span>Chiral NHC ligands and fluorination reagents<\/span><\/strong><\/li>\r\n<li><strong>Ring opening metathesis of strained fluorocycloalkenes<\/strong><\/li>\r\n<li><strong><span>Computational studies of reaction mechanisms<\/span><\/strong><\/li>\r\n<li><strong><span>Chiral fluorous recyclable ruthenium and palladium catalysts<\/span><\/strong><\/li>\r\n<\/ul>\r\n<p>We have developed polyfluoroalkylated Hoveyda-Grubbs second-generation precatalyst analogues and PEPPSI catalyst analogues, that can be recycled using medium fluorous separation methods. This approach utilizes hydrofluoroethers such as HFE 7100 or HFE 7500, which are environmentally acceptable in comparison to perfluorinated solvents.<br \/><img src=\"\/images\/450!0\/uzel\/0038642\/0002~~K0otTk0sSs4wBAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"237\" \/><br \/><br \/><\/p>\r\n<ul>\r\n<li><strong><span>Ring-closing metathesis of prochiral oxa<\/span><\/strong><strong>en<span>di<\/span><\/strong><strong>ynes<\/strong><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\">Prochiral oxaendiynes undergo chemoselective ring-closing metathesis affording 2<em>H<\/em>-pyran derivatives, which can be further transformed into tricyclic compounds via chemo- and stereoselective Diels-Alder reaction.<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0038642\/0001~~K0otTk0sSs4wAgA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"131\" \/><br \/><br \/><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38652"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38652":{"idvazba":"167974","nad_uzel":"136600","pod_uzel":"38652","url":"","sablona":"4","nazev":"Kvicala's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.03.2021 10:26:00","platne_do":null,"iduzel":"38652","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136609":{"idvazba":"167984","nad_uzel":"136600","pod_uzel":"136609","url":"\/research\/kvicala\/publications_clone_77589","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/kvicala\/publications_clone_77589}","poradi":"4","skupina_www":"everyone","platne_od":"12.05.2026 21:34:37.386001","platne_do":null,"iduzel":"136609","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:11886:\"<div id=\"hlavicka\">\r\n<h3 class=\"popis\">Selected publications<\/h3>\r\n<p><\/p>\r\n<p><strong>2020<\/strong><\/p>\r\n<p>Kolarikova, V.; Rybackova, M.; Svoboda, M.; Kvicala, J.:<br \/><span style=\"color: #333333; font-size: 15px;\">Ring-closing metathesis of prochiral oxaenediynes to racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2<\/span><em><span style=\"color: #333333; font-size: 15px;\">H<\/span><\/em><span style=\"color: #333333; font-size: 15px;\">-pyrans<br \/><em>Beilstein J. Org. Chem.&nbsp; <\/em><strong>2020<\/strong><em>, <i>16, <\/i><\/em>2757\u20132768 DOI:<a href=\"https:\/\/doi.org\/10.3762\/bjoc.16.226\" rel=\"follow\">10.3762\/bjoc.16.226<\/a><br \/><\/span><span style=\"color: #333333; font-size: 15px;\"><\/span><\/p>\r\n<p><\/p>\r\n<p>Simunek, O.; Rybackova, M.; Svoboda, M.; Kvicala, J.:<br \/>Synthesis, catalytic activity and medium fluorous recycle of fluorous analogues of PEPPSI catalysts<br \/><em>J. Fluorine Chem. <\/em><strong>2020<\/strong>, <em>236<\/em>, 109588 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2020.109588\" rel=\"follow\">10.1016\/j.jfluchem.2020.109588<\/a><\/p>\r\n<p><strong>2018<\/strong><\/p>\r\n<p>Mundil, R.; Sokolohorskyj, A.; Hosek, J.; Cvacka, J.; Cisarova, I.; Kvicala, J.; Merna, J.:<br \/>Nickel and palladium complexes with fluorinated alkyl substituted \u03b1-diimine ligands for living\/controlled olefin polymerization<br \/><span class=\"list__item-data\" aria-label=\"&lt;i&gt;&lt;strong&gt;Polym. Chem.&lt;\/strong&gt;&lt;\/i&gt;, 2018,&lt;span style='padding-right:2px'&gt;&lt;\/span&gt;&lt;strong&gt;9&lt;\/strong&gt;, 1234-1248\"> <em>Polym. Chem.<\/em> <strong>2018<\/strong>, <em>9<\/em>, 1234-1248 DOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C8PY00201K\" rel=\"follow\"><span class=\"list__item-data\">10.1039\/C8PY00201K<\/span><\/a><\/span><\/p>\r\n<p>Hosek, J.; Simunek, O.; Lipovska, P.; Kolarikova, V.; Kucnirova, K.; Edr, A.; Stepankova, N.; Rybackova, M.; Cvacka, J.; Kvicala, J.:<br \/><span class=\"hlFld-Title\">Medium Fluorous Separation Using Hydrofluoroether and Weakly Polar Solvents for Environmentally Friendly Recycling of Catalysts<br \/><span class=\"cit-info\"><em><span class=\"cit-journal-abbreviation\">ACS Sustainable Chem. Eng.<\/span><\/em><span class=\"cit-sperator\">&nbsp; <strong>2018<\/strong>, <\/span><em><span class=\"cit-volume\">6<\/span><\/em><span class=\"cit-sperator\">,<\/span> <span class=\"cit-pages\">7026-7034<\/span><\/span> DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acssuschemeng.8b00865\" rel=\"follow\">10.1021\/acssuschemeng.8b00865<\/a><br \/><\/span><\/p>\r\n<p><span class=\"hlFld-Title\">Kucnirova, K.; Simunek, O.; Rybackova, M.; Kvicala, J.:<br \/><\/span>Structural Assignment of Fluorocyclobutenes by <sup>19<\/sup>F NMR Spectroscopy \u2013 Comparison of Calculated <sup>19<\/sup>F NMR Shielding Constants with Experimental <sup>19<\/sup>F NMR Shifts<br \/><em>Eur. J. Org. Chem.<\/em> <strong>2018<\/strong>, 3867-3874 DOI:<a href=\"https:\/\/doi.org\/10.1002\/ejoc.201800482\" class=\"epub-doi\" rel=\"follow\">10.1002\/ejoc.201800482<\/a><\/p>\r\n<p><strong>2016<\/strong><\/p>\r\n<p>Lipovska, P.; Rathouska, L.; Simunek, O.; Hosek, J.; Kolarikova, V.; Rybackova, M.; Cvacka, J.; Svoboda, M.; Kvicala, J.:<br \/>Synthesis and catalytic activity of ruthenium complexes modified with chiral racemic per- and polyfluorooxaalkanoates<br \/><em>J. Fluorine Chem.<\/em> <strong>2016<\/strong>, <em>191<\/em>, 14-22 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2016.09.005\">10.1016\/j.jfluchem.2016.09.005<\/a><\/p>\r\n<p>Dolensk\u00fd, B.; Kv\u00ed\u010dala, J.; Paleta, O. &nbsp;Methyl fluoroalkanoate as methyl-\u200btransferring reagent. Unexpected participation of BAl2 (SN2) mechanism in the reaction of methyl 2,\u200b3,\u200b3,\u200b3-\u200btetrafluoro-\u200b2-\u200bmethoxypropanoate with amines. <em>J. Fluorine Chem.<\/em> <strong>2016<\/strong>, <em>185<\/em>, 31-35. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2016.02.012\">10.1016\/j.jfluchem.2016.02.012<\/a><\/p>\r\n<p><br \/><br \/><\/p>\r\n<h4><strong>2015<\/strong><\/h4>\r\n<p><\/p>\r\nKola\u0159\u00edkov\u00e1, V.; \u0160im\u016fnek, O.; Ryb\u00e1\u010dkov\u00e1, M.; Cva\u010dka, J.; B\u0159ezinov\u00e1, A.; Kv\u00ed\u010dala, J. Transition Metal Complexes Bearing NHC Ligands with Secondary Polyfluoroalkyl Groups. <em>J. Chem. Soc., Dalton Trans.<\/em>, <strong>2015<\/strong>,&nbsp;<em>44<\/em>, 19663-19673.&nbsp;DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5DT02258D%20\">10.1039\/C5DT02258D<span style=\"font-size: 12px; line-height: 20px; background-color: #ffffff;\">&nbsp;<\/span><\/a><\/div>\r\n<div>\r\n<p>&nbsp;<\/p>\r\n<p>Ryb\u00e1\u010dkov\u00e1, M.; Ho\u0161ek, J.; \u0160im\u016fnek, O.; Kola\u0159\u00edkov\u00e1, V.; Kv\u00ed\u010dala, J.&nbsp;Computational study of productive and non-productive cycles in fluoroalkene metathesis.&nbsp;<em>Beilstein J. Org. Chem.&nbsp;<\/em><strong>2015<\/strong>,&nbsp;<em>11<\/em>,&nbsp;2150\u20132157. DOI:<a href=\"http:\/\/dx.doi.org\/10.3762\/bjoc.11.232\">10.3762\/bjoc.11.232<\/a><\/p>\r\n<p>&nbsp;<\/p>\r\n<p><span style=\"background-color: #ffffff; font-size: small;\"><span style=\"text-align: right;\">&nbsp;<\/span><\/span>Ho\u0161ek, J.; Ryb\u00e1\u010dkov\u00e1, M.; \u010cejka, J.; Cva\u010dka, J.; Kv\u00ed\u010dala, J.: &nbsp;Synthesis of heavy Fluorous Ruthenium Metathesis catalysts using the stereoselective addition of polyfluoroalkyllithium to sterically hindered diimines. <em>Organometallics<\/em> <strong>2015<\/strong>, <em>34(13)<\/em>, 3327-3334. <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.organomet.5b00325\">DOI:10.1021\/acs.organomet.5b00325<\/a><\/p>\r\n<h3>&nbsp;<\/h3>\r\n<p><strong>2014<\/strong><\/p>\r\n<p><\/p>\r\n<p>Babun\u011bk, M.; \u0160im\u016fnek, O.; Ho\u0161ek, J.; Ryb\u00e1\u010dkov\u00e1, M.; Cva\u010dka, J.; B\u0159ezinov\u00e1, A.; Kv\u00ed\u010dala, J. Heavy fluorous phosphine-free ruthenium catalysts for alkene metathesis. <em>J. Fluorine Chem.<\/em>, <strong>2014<\/strong>, <em>161<\/em>, 66-75. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2014.03.003\" target=\"_blank\" id=\"ddDoi\" rel=\"noopener\">10.1016\/j.jfluchem.2014.03.003<\/a><\/p>\r\n<p><\/p>\r\n<p>&nbsp;<\/p>\r\n<\/div>\r\n<div id=\"hlavni\">\r\n<div id=\"publikace\">\r\n<h4><strong>2013<\/strong><\/h4>\r\n<p>&nbsp;<\/p>\r\n<p>Kv\u00ed\u010dala, J.; Schindler, M.; Kelbichov\u00e1, V.; Babun\u011bk, M; Ryb\u00e1\u010dkov\u00e1, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; B\u0159ezinov\u00e1, A.: Experimental and theoretical study of Hoveyda-Grubbs catalysts modified by perfluorohexyl ponytail in the alkoxybenzylidene ligand. <em>J. Fluorine Chem.<\/em>, <strong>2013<\/strong>, <em>153<\/em>, 12-25. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2013.06.001\">DOI:10.1016\/j.jfluchem.2013.06.001<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2012<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Skalick\u00fd, M.; Skalick\u00e1, V.; Paterov\u00e1, J.; Ryb\u00e1\u010dkov\u00e1, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; B\u0159ezinov\u00e1, A.; Kv\u00ed\u010dala, J.: Ag Complexes of NHC ligands Bering Polyfluoroalkyl and\/or Polyfluoropolyalkoxy Ponytails. Why Are Polyethers More Fluorous Than Alkyls. <em>Organometallics<\/em>, <strong>2012<\/strong>, <em>31<\/em>, 1524-1532. <a href=\"http:\/\/dx.doi.org\/10.1021\/om201062c\">DOI:10.1021\/om201062c<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2011<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Skalick\u00e1, V.; Ryb\u00e1\u010dkov\u00e1, M.; Skalick\u00fd, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; B\u0159ezinov\u00e1, A.; \u010cejka, J.; Kv\u00ed\u010dala, J.: Polyfluoroalkylated Tripyrazolylmethane Ligands: Synthesis and Complexes. <em>J. Fluorine Chem<\/em>. <strong>2011<\/strong>, <em>132<\/em>, 434-440. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2011.04.010\">DOI:10.1016\/j.jfluchem.2011.04.010<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2010<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Paterov\u00e1, J.; Skalick\u00fd, M.; Ryb\u00e1\u010dkov\u00e1, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; Kv\u00ed\u010dala, J.: Synthesis of 2-(perfluoroalkyl)ethyl potassium sulfates based on perfluorinated Grignard reagents. <em>J. Fluorine Chem<\/em>. <strong>2010<\/strong>, <em>131<\/em>, 1338-1343. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2010.09.004\">DOI:10.1016\/j.jfluchem.2010.09.003<\/a><\/p>\r\n<p>Kv\u00ed\u010dala, J.; Bene\u0161, M.; Paleta, O.; Kr\u00e1l, V.: Regiospecific nucleophilic substitution in 2,3,4,5,6-pentafluorobiphenyl as model compound for supramolecular systems. Theoretical study of transition states and energy profiles, evidence for tetrahedral S<sub><small>N<\/small><\/sub>2 mechanism. <em>J. Fluorine Chem<\/em>. <strong>2010<\/strong>, <em>131<\/em>, 1327-1337. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2010.09.003\">DOI:10.1016\/j.jfluchem.2010.09.003<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2009<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Skalick\u00fd, M.; Ryb\u00e1\u010dkov\u00e1, M.; Kysilka, O.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; \u010cejka, J.; Kv\u00ed\u010dala, J.: Synthesis of bis(polyfluoroalkylated)imidazolium salts as key intermediates for fluorous NHC ligands. <em>J. Fluorine Chem.<\/em> <strong>2009<\/strong>, <em>130<\/em>, 966-973. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2009.07.015\">DOI:10.1016\/j.jfluchem.2009.07.015<\/a><\/p>\r\n<p>Kysilka, O.; Ryb\u00e1\u010dkov\u00e1, M.; Skalick\u00fd, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; Kv\u00ed\u010dala, J.: Fluorous imidazolium room-temperature ionic liquids based on HFPO trimer. <em>J. Fluorine Chem<\/em>. <strong>2009<\/strong>, <em>130<\/em>, 629-639. <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jfluchem.2009.04.006\">DOI:10.1016\/j.jfluchem.2009.04.006<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2008<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Kysilka, O.; Ryb\u00e1\u010dkov\u00e1, M.; Skalick\u00fd, M.; Kv\u00ed\u010dalov\u00e1, M.; Cva\u010dka, J.; Kv\u00ed\u010dala, J.: HFPO trimer-based alkyl triflate, a novel building block for fluorous chemistry. Preparation, reactions and 19F gCOSY analysis. <em>Collect. Czech. Chem. Commun<\/em>. <strong>2008<\/strong>, <em>73(12)<\/em>, 1799-1813. <a href=\"http:\/\/dx.doi.org\/10.1135\/cccc20081799\">DOI:10.1135\/cccc20081799<\/a><\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2007<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Pomeisl, K.; \u010cejka, J.; Kv\u00ed\u010dala, J.; Paleta, O.: Synthesis of 3-fluorofuran-2(5H)-ones based on Z\/E photoisomerisation and cyclisation of 2-fluoro-4-hydroxybut-2-enoates. <em>Eur. J. Org. Chem.<\/em> <strong>2007<\/strong>, 5917-5925.<\/p>\r\n<p>Hajduch, J.; Paleta, O.; Kv\u00ed\u010dala, J.; Haufe, G.: Fluorinated furan-2(5H)-ones: reactivity and stereoselectivity in Diels-Alder reactions. <em>Eur. J. Org. Chem<\/em>. <strong>2007<\/strong>, 5101-5111.<\/p>\r\n<p>Pomeisl, K.; Kv\u00ed\u010dala, J.; Paleta, O.; Kl\u00e1sek, A; Kafka, S.; Kubelka, V.; Havl\u00ed\u010dek, J.; \u010cejka, J.: Limitations of the Wittig-Horner-type annulation of fluorobutenolide moiety to 3-hydroxyquinoline-2,4(2H,3H)-diones. Novel modifications of the Perkow reaction including fluorinated acyloxy leaving groups. <em>Tetrahedron<\/em> <strong>2007<\/strong>, <em>63<\/em>, 10549-10561.<\/p>\r\n<p>\u010cervenkov\u00e1 \u0160\u0165astn\u00e1 L.; Auerov\u00e1, K.; Kv\u00ed\u010dala, J.; \u010cerm\u00e1k, J.: Fluorophilic properties of (perfluorooctyl)ethyldimethylsilyl substituted and tetramethyl(perfluoroalkyl) substituted cyclopentadienes and their Ti(IV), Rh(III), and Rh(I) complexes. <em>J. Organomet. Chem.<\/em> <strong>2007<\/strong>, <em>692<\/em>, 1974-1982.<\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2006<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Pomeisl, K.; Kv\u00ed\u010dala, J.; Paleta, O.: Convenient Synthesis of 3-Fluoro-4,5-diphenylfuran-2(5H)-one from Benzoin Ethers. Novel and Efficient Z-E Isomerisation and Cyclisation of 2-Fluoroalkenoate Precursors, Substitution of Vinylic Fluorine. <em>J. Fluorine Chem<\/em>. <strong>2006<\/strong>, <em>127<\/em>, 1390-1397.<\/p>\r\n<p>Kv\u00ed\u010dala, J.; Baszczy\u0148ski, O.; Krupkov\u00e1, A.; Str\u00e1nsk\u00e1, D.: Hydroboration of 1,1\u2019-Bi(cyclopent-1-ene) and 3,3\u2019-Biindene: Experimental and Theoretical Study. <em>Collect. Czech Chem. Commun.<\/em> <strong>2006<\/strong>, <em>71<\/em>, 1611-1626.<\/p>\r\n<h4>&nbsp;<\/h4>\r\n<h4><strong>2005<\/strong><\/h4>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p>Kv\u00ed\u010dala, J.; \u0160tambask\u00fd, J.; Skalick\u00fd, M.; Paleta, O.: Preparation of Fluorohalomethyl-magnesium Halides Using Highly Active Magnesium Metal and Their Reactions. <em>J. Fluorine Chem<\/em>. <strong>2005<\/strong>, <em>126<\/em>, 1390-1395.<\/p>\r\n<p>Dolensk\u00fd, B.; Kv\u00ed\u010dala, J.; Paleta, O.: Methyl 3,3,3-Trifluoropyruvate Hemiaminals: Stability and Transaminations. <em>J. Fluorine Chem<\/em>. <strong>2005<\/strong>, <em>126<\/em>, 745-751.<\/p>\r\n<\/div>\r\n<\/div>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38652"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38652":{"idvazba":"167974","nad_uzel":"136600","pod_uzel":"38652","url":"","sablona":"4","nazev":"Kvicala's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"02.03.2021 10:26:00","platne_do":null,"iduzel":"38652","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136610":{"idvazba":"168064","nad_uzel":"116995","pod_uzel":"136610","url":"\/research\/lhotak-budka","sablona":"58","nazev":"Lhot\u00e1k Research Group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/lhotak-budka}","poradi":"8","skupina_www":"everyone","platne_od":"03.06.2026 14:03:00","platne_do":null,"iduzel":"136610","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:22:\"Lhot\u00e1k Research Group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:4:\"atom\";s:7:\"obrazek\";s:34:\"0004~~y0hNTIl39Yuvyk3NK07NqwQA.png\";s:5:\"vyska\";s:2:\"sm\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:931:\"<h2 style=\"text-align: center;\"><span class=\"weburl\">Supramolecular Chemistry Group<\/span><\/h2>\r\n<h2 style=\"text-align: center;\"><span class=\"weburl\"> at DOC UCT Prague<\/span><\/h2>\r\n<p><\/p>\r\n<p>Anyone who&nbsp;might be interested in calixarene and\/or supramolecular chemistry, please contact Prof. Pavel Lhot\u00e1k via e-mail: <a href=\"mailto:lhotakp@vscht.cz\">lhotakp@vscht.cz<\/a>&nbsp;or tel.: +420 220 445 055.<\/p>\r\n<p><\/p>\r\n<p><img src=\"\/files\/uzel\/0136610\/y8nIL0nMjnfOSM11zs_NjU_OL0stii_ITC4pLUo1MAQA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"Chem. 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Chem. 2016, 40, 1104-1110, http:\/\/dx.doi.org\/10.1039\/C5NJ02427G\" width=\"215\" height=\"215\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_obrazek","autonomni":"1","pod_uzly":["22327","22325","136611","136624","136625"],"poduzly_count":5,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":1,"22327":{"idvazba":"168008","nad_uzel":"136625","pod_uzel":"22327","url":"","sablona":"4","nazev":"Lhotak's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:58:00","platne_do":null,"iduzel":"22327","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"22325":{"idvazba":"168003","nad_uzel":"136611","pod_uzel":"22325","url":"","sablona":"20","nazev":"Slider","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"18.09.2015 16:26:41.264744","platne_do":null,"iduzel":"22325","obsah":"N;","class":"slider","autonomni":"0","pod_uzly":["22326","22326"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22326":{"idvazba":"27913","nad_uzel":"22325","pod_uzel":"22326","url":"","sablona":"20","nazev":"Slide main","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:44:00","platne_do":null,"iduzel":"22326","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:11:\"head_EN.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136611":{"idvazba":"170770","nad_uzel":"136610","pod_uzel":"136611","url":"\/research\/lhotak-budka\/people","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/lhotak-budka\/people}","poradi":"2","skupina_www":"everyone","platne_od":"30.06.2026 12:25:00","platne_do":null,"iduzel":"136611","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:8047:\"<p><\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0136611\/0007~~8_R11zUyMDIyNDIy1g13NDAwMAIA.jpg\" alt=\" \u25f3 IMG-20221223-WA0002 (jpg) \u2192 (origin\u00e1l)\" width=\"800\" height=\"600\"><\/p>\r\n<table id=\"AutoNumber1\" class=\"table_bezramecku\" style=\"border-color: rgb(255, 255, 255); width: 78.5143%; height: 446.805px;\" width=\"100%\" cellspacing=\"0\" cellpadding=\"0\" border=\"0\">\r\n<tbody>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"16%\">\r\n<h4><span class=\"modra0\">Group Leader:<\/span><\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"47%\">\r\n<h3><a href=\"\/files\/uzel\/0136611\/0011~~88nILzm8MBsA.pdf\">Prof. Pavel Lhot\u00e1k<\/a><\/h3>\r\n<\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4>&nbsp;<\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4><span class=\"modra0\">Associate Professor:&nbsp;<\/span><\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">\r\n<h3>&nbsp;<a href=\"\/files\/uzel\/0136611\/0010~~cypNyU4EAA.pdf\">Assoc. Prof. Jan Budka<\/a><\/h3>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4>&nbsp;<\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4><span class=\"modra0\">Assistent Professor:<\/span><\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">\r\n<h3>&nbsp;Dr. Ond\u0159ej Kundr\u00e1t<\/h3>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"width: 21.545%; height: 19.1944px;\">\r\n<h4><\/h4>\r\n<\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\">\r\n<h3>&nbsp;<a href=\"\/files\/uzel\/0136611\/0008~~C8kpLS45vDfe1Q8A.pdf\">Dr. Martin Tlust\u00fd<\/a><\/h3>\r\n<\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4>&nbsp;<\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"width: 21.545%; height: 19.1944px;\">\r\n<h4><span class=\"modra0\">PostDoc:<\/span><\/h4>\r\n<\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\">\r\n<h3>&nbsp;Dr. Daniel Kortus<\/h3>\r\n<\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"width: 21.545%; height: 19.1944px;\">\r\n<h4><\/h4>\r\n<\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\"><\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4><span class=\"modra0\">PhD Students:&nbsp;<\/span><\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">&nbsp;<\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\">&nbsp;MSc. Anastasia Surina (06)<\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"width: 21.545%; height: 19.1944px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\">&nbsp;MSc. &nbsp;Michal Chur\u00fd (D2)<\/td>\r\n<td style=\"width: 19.5684%; height: 19.1944px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 0px;\">\r\n<td style=\"width: 21.545%; height: 0px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 0px;\"><\/td>\r\n<td style=\"width: 19.5684%; height: 0px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4><span class=\"modra0\">Students:&nbsp;&nbsp;<\/span><\/h4>\r\n<\/td>\r\n<td style=\"width: 58.903%; height: 19.1944px;\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Jaroslav Nedbal\u00fd (M1)<\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\">&nbsp;<\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Monika Ne\u0161n\u011brov\u00e1 (M1)<\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Tade\u00e1\u0161 Petr\u016f (B3)<\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Luk\u00e1\u0161 Smejkal (B3)<br><\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Libor Kucha\u0159 (B3)<br><\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 20.0833px;\">\r\n<td style=\"width: 21.545%; height: 20.0833px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 20.0833px;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Karla Hovorkov\u00e1 (B3)<br><\/span><\/td>\r\n<td style=\"width: 19.5684%; height: 20.0833px;\"><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 21.545%;\"><\/td>\r\n<td style=\"width: 58.903%;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Jan Kalou\u0161 (B2)<\/span><\/td>\r\n<td style=\"width: 19.5684%;\"><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 21.545%;\"><\/td>\r\n<td style=\"width: 58.903%;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Timotej Hloch (B2)<\/span><\/td>\r\n<td style=\"width: 19.5684%;\"><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 21.545%;\"><\/td>\r\n<td style=\"width: 58.903%;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;Karol\u00edna Ku\u0159\u00edkov\u00e1 (B2)<\/span><\/td>\r\n<td style=\"width: 19.5684%;\"><\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 21.545%;\"><\/td>\r\n<td style=\"width: 58.903%;\"><span style=\"font-family: 'Calibri', sans-serif, serif, 'EmojiFont';\" lang=\"CS\">&nbsp;David \u0160ebesta (B2)<\/span><\/td>\r\n<td style=\"width: 19.5684%;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 0px;\">\r\n<td style=\"width: 21.545%; height: 0px;\"><\/td>\r\n<td style=\"width: 58.903%; height: 0px;\"><\/td>\r\n<td style=\"width: 19.5684%; height: 0px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">\r\n<h4><span class=\"modra0\">Technician:<\/span><\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">\r\n<h4>&nbsp;Nataliia Markovska<\/h4>\r\n<\/td>\r\n<td style=\"height: 19.1944px; width: 19.5684%;\" width=\"13%\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19.1944px;\">\r\n<td style=\"height: 19.1944px; width: 21.545%;\" width=\"24%\">&nbsp;<\/td>\r\n<td style=\"height: 19.1944px; width: 58.903%;\" width=\"16%\">&nbsp;<\/td>\r\n<td style=\"width: 19.5684%; height: 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Students\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136623":{"idvazba":"168002","nad_uzel":"136616","pod_uzel":"136623","url":"","sablona":"11","nazev":"technician","_url_prefix":null,"poradi":"6","skupina_www":"everyone","platne_od":"12.05.2026 21:34:58.639315","platne_do":null,"iduzel":"136623","obsah":"a:4:{s:6:\"nadpis\";s:10:\"Technician\";s:8:\"velikost\";s:2:\"sm\";s:6:\"slider\";s:1:\"0\";s:7:\"bg_gray\";s:1:\"0\";}","class":"galerie","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"22325":{"idvazba":"168003","nad_uzel":"136611","pod_uzel":"22325","url":"","sablona":"20","nazev":"Slider","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"18.09.2015 16:26:41.264744","platne_do":null,"iduzel":"22325","obsah":"N;","class":"slider","autonomni":"0","pod_uzly":["22326","22326"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22326":{"idvazba":"27913","nad_uzel":"22325","pod_uzel":"22326","url":"","sablona":"20","nazev":"Slide main","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:44:00","platne_do":null,"iduzel":"22326","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:11:\"head_EN.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136624":{"idvazba":"168004","nad_uzel":"136610","pod_uzel":"136624","url":"\/research\/lhotak-budka\/research_clone_84217","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/lhotak-budka\/research_clone_84217}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:34:58.687335","platne_do":null,"iduzel":"136624","obsah":"a:6:{s:5:\"nazev\";s:19:\"Our recent research\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:6689:\"<table class=\"table_bezramecku\" style=\"height: 128px;\" width=\"619\">\r\n<tbody>\r\n<tr>\r\n<td style=\"text-align: justify;\"><span style=\"color: #808080; font-family: Verdana; font-size: small;\"><span class=\"cerna0\">In the last years, we have been focusing on inherently chiral derivatives which can be obtained via relatively simple reactions in the meta-position of a (thia)caliarene skeleton (see <a href=\"research-groups\/lhotak-en\/publications\">publications<\/a>); some examples of last results:<\/span><\/span><\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\u00a0<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\r\n<h4 class=\"articleTitle\" style=\"margin-top: 0px; margin-bottom: 0px; text-align: center;\" align=\"center\"><strong><span class=\"cervena0\"><span class=\"cerna0\">I<\/span><span class=\"cerna0\">ntramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds<\/span><\/span><\/strong><\/h4>\r\n<h4 class=\"articleTitle\" style=\"margin-top: 0px; margin-bottom: 0px; text-align: center;\" align=\"center\">Slavik, P.; Eigner, V.; Lhotak, P.<br \/><em>Org. Lett.<\/em> <strong>2015<\/strong>, <em>17<\/em>,\u00a02788-2791<br \/>\u00a0<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.5b01200\">DOI:10.1021\/acs.orglett.5b01200<\/a>\u00a0<\/h4>\r\n<br class=\"cerna0\" \/>\r\n<h4 class=\"articleTitle\" style=\"margin-top: 0px; margin-bottom: 0px; text-align: center;\"><img src=\"http:\/\/pubs.acs.org\/appl\/literatum\/publisher\/achs\/journals\/content\/orlef7\/2015\/orlef7.2015.17.issue-11\/acs.orglett.5b01200\/20150601\/images\/medium\/ol-2015-01200p_0010.gif\" alt=\"Abstract Image\" \/>\u00a0<\/h4>\r\n<p style=\"text-align: justify;\"><span style=\"color: #808080; font-family: Verdana; font-size: small;\"><span class=\"cerna0\"><span style=\"text-decoration: underline;\">Abstract<\/span>: Regioselective derivatization via an organomercury intermediate allowed for the introduction of carboxylic acid functionality into the <em>meta<\/em> position of the calix[4]arene skeleton. Intramolecular Friedel\u2013Crafts cyclization led to a novel type of calixarene containing a ketone bridging moiety. Subsequent attack of the ketone by organometallic compounds occurred selectively from outside providing tertiary alcohols with the OH group oriented inside the cavity. These compounds can complex neutral molecules both in the solid state (X-ray) and in solution (NMR) using the cooperative effect of hydrogen bonding (OH) and CH\u2212\u03c0 interactions from within the cavity.<br \/><\/span><\/span><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\u00a0<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\r\n<p style=\"text-align: center;\"><strong><span class=\"zelena0\"><span class=\"cerna0\"><span class=\"cervena0\"><span class=\"cerna0\">Shaping of Calix[4]arenes via Double Bridging of the Upper Rim<\/span><\/span><\/span><\/span><\/strong><\/p>\r\n<p style=\"text-align: center;\"><span class=\"zelena0\"><span class=\"cerna0\">Slavik, P.; Eigner, V.; Lhotak, P.<br \/><em>Cryst. Eng. Comm.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 4964-4970 <br \/>DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6CE00314A\">10.1039\/C6CE00314A<\/a><\/span><\/span><\/p>\r\n<h4 style=\"text-align: center;\">\u00a0<\/h4>\r\n<p style=\"margin-top: 0; margin-bottom: 0;\"><img src=\"http:\/\/pubs.rsc.org\/services\/images\/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc\/ImageService\/image\/GA?id=C6CE00314A\" id=\"imgGALoader\" title=\"Graphical abstract\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"Graphical abstract: Shaping of calix[4]arenes via double bridging of the upper rim\" \/>\u00a0<\/p>\r\n<p style=\"margin-top: 0; margin-bottom: 0;\">\u00a0<\/p>\r\n<p style=\"margin-top: 0px; margin-bottom: 0px; text-align: justify;\"><span style=\"color: #808080; font-family: Verdana; font-size: small;\"><span class=\"cerna0\"><span style=\"text-decoration: underline;\">Abstract<\/span>: Direct double <em>meta<\/em>-mercuration can be used for subsequent bridging of a calix[4]arene skeleton <em>via<\/em> the installation of ketone moieties. This unprecedented substitution pattern in calixarene chemistry possesses a heavily distorted and rigid cavity capable of interactions with selected molecular guests as documented by binding of a CH<small><sub>2<\/sub><\/small>Cl<small><sub>2<\/sub><\/small> molecule held in place by an intricate net of 10 specific (halogen bonding and hydrogen bonding) interactions from two neighbouring calixarene molecules<br \/><\/span><\/span><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\u00a0<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\r\n<h4 style=\"text-align: center;\"><strong><span class=\"cerna0\"><span class=\"\"><br \/>Calix[4]arene Containing a Ureido Functionality on the Lower Rim as Highly Efficient Receptors for Anion Recognition<br \/><\/span><\/span><\/strong><\/h4>\r\n<h4 style=\"text-align: center;\"><span class=\"cerna0\"><span class=\"\">Klejch, T.; Slavicek, J.; Hudecek, O.; Eigner, V.; Gutierrez, N. A.; Curinova, P.; Lhotak, P.<\/span><\/span><\/h4>\r\n<h4 style=\"text-align: center;\"><span class=\"cerna0\"><span class=\"\"><em>New J. Chem.<\/em><\/span><\/span> <strong><span class=\"cerna0\"><span class=\"\">2016, <\/span><\/span><\/strong><span class=\"cerna0\"><span class=\"\"><em>40<\/em><\/span><\/span><span class=\"cerna0\"><span class=\"\">, 7935-7942<br \/>\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c6nj01271j\">10.1039\/c6nj01271j<\/a><\/span><\/span><span class=\"cerna0\"><br \/><\/span><strong><span class=\"cerna0\"><br class=\"cerna0\" \/><\/span><\/strong><\/h4>\r\n<p><strong><span class=\"cerna0\"><img src=\"http:\/\/pubs.rsc.org\/services\/images\/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc\/ImageService\/image\/GA?id=C6NJ01271J\" id=\"imgGALoader\" title=\"Graphical abstract\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"Graphical abstract: Calix[4]arenes containing a ureido functionality on the lower rim as highly efficient receptors for anion recognition\" \/><\/span><\/strong><\/p>\r\n<p>\u00a0<\/p>\r\n<p style=\"text-align: justify;\"><span style=\"color: #808080; font-family: Verdana; font-size: small;\"><span class=\"cerna0\"><span style=\"text-decoration: underline;\">Abstract<\/span>: The introduction of nosyl moieties onto the lower rim of the calix[4]arene skeleton led to the formation of compounds immobilised in <em>cone<\/em> conformations. Subsequent reduction of the nitro group and reaction with aryl isocyanates enabled the construction of new calixarene-based ligands for anion recognition. As proven by NMR and UV\/vis titration experiments, diaryl urea moieties with electron-withdrawing substituents on both sides represent very efficient tools for the complexation of selected anions (AcO<small><sup>\u2212<\/sup><\/small>, BzO<small><sup>\u2212<\/sup><\/small>, H<small><sub>2<\/sub><\/small>PO<small><sub>4<\/sub><\/small><small><sup>\u2212<\/sup><\/small>) even in highly competitive solvents such as DMSO-d<small><sub>6<\/sub><\/small>.<br \/><\/span><\/span><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td>\u00a0<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><\/p>\";}","class":"stranka","autonomni":"1","pod_uzly":["22327","22325"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22327":{"idvazba":"168008","nad_uzel":"136625","pod_uzel":"22327","url":"","sablona":"4","nazev":"Lhotak's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:58:00","platne_do":null,"iduzel":"22327","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"22325":{"idvazba":"168003","nad_uzel":"136611","pod_uzel":"22325","url":"","sablona":"20","nazev":"Slider","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"18.09.2015 16:26:41.264744","platne_do":null,"iduzel":"22325","obsah":"N;","class":"slider","autonomni":"0","pod_uzly":["22326","22326"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22326":{"idvazba":"27913","nad_uzel":"22325","pod_uzel":"22326","url":"","sablona":"20","nazev":"Slide main","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:44:00","platne_do":null,"iduzel":"22326","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:11:\"head_EN.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136625":{"idvazba":"174971","nad_uzel":"136610","pod_uzel":"136625","url":"\/research\/lhotak-budka\/publications","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/lhotak-budka\/publications}","poradi":"4","skupina_www":"everyone","platne_od":"02.07.2026 13:51:00","platne_do":null,"iduzel":"136625","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:54550:\"<h2><strong>2022:<\/strong><\/h2>\r\n<p>Li\u0161ka, A.; \u0158ezankov\u00e1, M.; Kl\u00edma, J.; Urban, J.; Budka, J.; Ludv\u00edk, J.: <br><span class=\"cervena0\">Electrochemical, EPR, and quantum chemical study of reductive cleavage of cone-Calix[4]arene nosylates \u2013 New electrosynthetic approach<\/span><br>Electrochem. Sci. Adv. <strong>2022<\/strong>, e2100221, DOI: org\/10.1002\/elsa.202100221<\/p>\r\n<h2><strong>2021:<\/strong><\/h2>\r\n<p>Kortus, D.; Krizova, K.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Synthesis of 2,8-dithiacalix[4]arene based on fragment condensation<\/span><br><em>Tetrahedron Lett<\/em>. <strong>2021<\/strong>, <em>69<\/em>, 152924 DOI:<a href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2021.152924\">10.1016\/j.tetlet.2021.152924<\/a><\/p>\r\n<p>Kortus, D.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Regio- and stereoselectivity of spirodienone formation in 2,14-dithiacalix[4]arene<\/span><br><em>New J. Chem.<\/em> <strong>2021<\/strong>, <em>45<\/em>, 8563-8571 DOI:<a href=\"https:\/\/doi.org\/10.1039\/d1nj01257f\">10.1039\/d1nj01257f<\/a><\/p>\r\n<p>Kortus, D.; Kundrat, O.; Cejka, J.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Chemistry of 2,14-Dithiacalix[4]arene: Searching for the Missing Fifth Conformer<\/span><br><em>J. Org. Chem.<\/em> <strong>2021<\/strong> DOI:<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.1c01173\">10.1021\/acs.joc.1c01173<\/a><\/p>\r\n<p>Curinova, P.; Winkler, M.; Krupkova, A.; Cisarova, I.; Budka, J.; Wun, C.N.; Blechta, V.; Maly, M.; Stastna-Cervenkova, L.; Sykora, J.; Strasak, T.:<br><span class=\"cervena0\">Transport of Anions across the Dialytic Membrane Induced by Complexation toward Dendritic Receptors<\/span><br><em>ACS Omega<\/em> <strong>2021<\/strong>, <em>23<\/em>, 15514-15522 DOI:10.1021\/acsomega.1c02142<\/p>\r\n<h2><strong>2020:<\/strong><\/h2>\r\n<p>Horackova, T.; Budka, J.; Eigner, V.; Chung, W.-S.; Curinova, P.; Lhotak, P.: <br><span class=\"cervena0\">Chiral anion recognition using calix[4]arene-based ureido receptors in a 1,3-alternate conformation<\/span> <br><em>Beilstein J. Org. Chem. <\/em><strong>2020<\/strong>, <em>16<\/em>, 2999-3007 DOI:<a href=\"https:\/\/doi.org\/10.3762\/bjoc.16.249\">10.3762\/bjoc.16.249<\/a><\/p>\r\n<p>Landovsky, T.; Eigner, V.; Babor, M.; Tichotova, M.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective S<sub>N<\/sub>Ar reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton<\/span><br><em>Chem. Commun.<\/em> <strong>2020<\/strong>, <em>56<\/em>, 78-81 DOI:<a href=\"https:\/\/doi.org\/10.1039\/c9cc08335a\">10.1039\/c9cc08335a<\/a><\/p>\r\n<p>Tlusty, M.; Dvorakova, H.; Cejka, J.; Kohout, M.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective formation of the quinazoline moiety on the upper rim of calix[4]arene as a route to inherently chiral systems<\/span><br><em>New J. Chem.<\/em> <strong>2020<\/strong>, <em>44<\/em>, 6490-6500 DOI:<a href=\"https:\/\/doi.org\/10.1039\/d0nj01035a\">10.1039\/d0nj01035a<\/a><\/p>\r\n<p>Kortus, D.; Kundrat, O.; Tlusty, M.; Cejka, J.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Inherent chirality through a simple dialkylation of 2,14-dithiacalix[4]arene<\/span><br><em>New J. Chem.<\/em> <strong>2020<\/strong>, <em>44<\/em>, 14496-14504 DOI:<a href=\"https:\/\/doi.org\/10.1039\/d0nj03468a\">10.1039\/d0nj03468a<\/a><\/p>\r\n<p>Tlusty, M.; Spalovska, D.; Kohout, M.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes<\/span><br><em>Chem. Commun.<\/em> <strong>2020<\/strong>, <em>56<\/em>, 12773-12776 DOI:<a href=\"https:\/\/doi.org\/10.1039\/d0cc05352j\">10.1039\/d0cc05352j<\/a><\/p>\r\n<p>Shishkanova, T.V.; Vatrskova, L.; Spalovska, D.; Kralik, F.; Curinova, P.; Winkler, M.; Budka, J.; Jurasek, B.; Kuchar, M.; Setnicka, V.:<br><span class=\"cervena0\">Complexation of cathinones by 4-<em>tert<\/em>-butylcalix[4]arene tetra-acetate as a possible technique for forensic analysis<\/span><br><em>Forensic Toxicol.<\/em> <strong>2020<\/strong>, <em>38<\/em>, 70-78 DOI:10.1007\/s11419-019-00489-8<\/p>\r\n<h2><strong>2019:<\/strong><\/h2>\r\n<p>Tlusty, M.; Spalovska, D.; Babor, M.; Lhotak, P.:<br><span class=\"cervena0\">Synthesis of enantiomerically pure inherently chiral calix[4]arenes using the meta-substitution strategy<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2019<\/strong>, <em>60<\/em>, 260-263 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2018.12.026\">10.1016\/j.tetlet.2018.12.026<\/a><\/p>\r\n<p>Slavik, P.; Krupicka, M.; Eigner, V.; Vrzal, L.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Rearrangement of <em>meta-<\/em>Bridged Calix[4]arenes Promoted by Internal Strain<\/span><br><em>J. Org. Chem.<\/em> <strong>2019<\/strong>, <em>84<\/em>, 4229-4235, DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.joc.9b00107\">10.1021\/acs.joc.9b00107<\/a><\/p>\r\n<p>Kortus, D.; Miksatko, J.; Kundrat, O.; Babor, M.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Chemistry of 2,14-Dithiacalix[4]arene: Alkylation and Conformational Behavior of Peralkylated Products<\/span><br><em>J. Org. Chem.<\/em> <strong>2019<\/strong>, <em>84<\/em>, 11572-11580, DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.joc.9b01493\">10.1021\/acs.joc.9b01493<\/a><\/p>\r\n<p>Tlusty, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhotak, P.:<br><span class=\"cervena0\">Synthesis of Upper Rim-double-bridged Calix[4]arenes bearing Seven Membered Rings and Related Compounds<\/span><br><em>RSC Advances<\/em> <strong>2019<\/strong>, <em>9<\/em>, 22017-22030 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c9ra05075b\">10.1039\/c9ra05075b<\/a><\/p>\r\n<h2><strong>2018:<\/strong><\/h2>\r\n<p>Landovsky, T.; Dvorakova, H.; Eigner, V.; Babor, M.; Krupicka, M.; Kohout, M.; Lhotak, P.:<br><span class=\"cervena0\">Chemoselective Oxidation of Phenoxathiin-based Thiacalix[4]arene and the Stereoselective Alkylation of Products<\/span><br><em>New J. Chem.<\/em> <strong>2018<\/strong>, <em>42<\/em>, 20074-20086 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C8NJ04690E\">10.1039\/C8NJ04690E<\/a><\/p>\r\n<p>Slavik, P.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">meta-Bridged calix[4]arenes with the methylene moiety possessing in\/out stereochemistry of substituents<\/span><br><em>New J. Chem.<\/em> <strong>2018<\/strong>, <em>42<\/em>, 16646-16652 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c8nj02577k\">10.1039\/c8nj02577k<\/a><\/p>\r\n<p>Landovsky, T.; Tichotova, M.; Vrzal, L.; Budka, J.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Structure elucidation of phenoxathiin-based thiacalix[4]arene conformations using NOE and RDC data<\/span><br><em>Tetrahedron<\/em> <strong>2018<\/strong>, <em>74<\/em>, 902-907 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2018.01.020\">10.1016\/j.tet.2018.01.020<\/a><\/p>\r\n<p>Slavik, P.; Dvorakova, H.; Krupicka, M.; Lhotak, P.:<br><span class=\"cervena0\">Unexpected cleavage of upper rim-bridged calix[4]arenes leading to linear oligophenolic derivatives<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2018<\/strong>, <em>59<\/em>, 838-843 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7OB03101G\">10.1039\/C7OB03101G<\/a><\/p>\r\n<p>Slavik, P.; Lhotak, P.:<br><span class=\"cervena0\">Unusual reactivity of upper-rim bridged calix[4]arenes - Friedel-Crafts alkylation via cleavage of the macrocyclic skeleton<\/span><br><em>Tetrahedron<\/em> <strong>2018<\/strong>, <em>59<\/em>, 1757-1759 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2018.03.072\">10.1016\/j.tetlet.2018.03.072<\/a><\/p>\r\n<h2><strong>2017:<\/strong><\/h2>\r\n<p>Bregier, F.; Hudecek, O.; Chaux, F.; Penouilh, M.; Chambron, J.; Lhotak, P.; Aubert, E.; Espinosa, E.:<br><span class=\"cervena0\">Generation of Cryptophanes in Water by Disulfide Bridge Formation<\/span><br><em>Eur. J. Org. Chem.<\/em> <strong>2017<\/strong>, 3795-3811 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201700537\">10.1002\/ejoc.201700537<\/a><\/p>\r\n<p>Tlusty, M.; Slavik, P.; Kohout, M.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring<\/span><br><em>Org. Lett.<\/em> <strong>2017<\/strong>, <em>19<\/em>, 2933-2936 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b01170\">10.1021\/acs.orglett.7b01170<\/a><\/p>\r\n<p>Slavik, P.; Eigner, V.; Bohm, S.; Lhotak, P.:<br><span class=\"cervena0\">Mercuration of Calix[4]arene Immobilized in the 1,2- and 1,3-Alternate Conformations<\/span><br><em>Tetrahedron Letters<\/em> <strong>2017<\/strong>, <em>58<\/em>, 1846-1850 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2017.03.085\">10.1016\/j.tetlet.2017.03.085<\/a><\/p>\r\n<p>Miksatko, J.; Eigner, V.; Kohout, M.; Lhotak, P.:<br><span class=\"cervena0\">Regio-\/stereoselective Formation of Monosulfoxides from Thiacalix[4]arenes in All Possible Conformations<\/span><br><em>Tetrahedron Letters<\/em> <strong>2017<\/strong>, <em>58<\/em>, 1687-1691 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2017.03.043\">10.1016\/j.tetlet.2017.03.043<\/a><\/p>\r\n<p>Tlusty, M.; Slavik, P.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Synthesis and Study of Calix[4]arenes bearing Azo Moieties at the <em>meta<\/em> Position<\/span><br><em>Tetrahedron<\/em> <strong>2017<\/strong>, <em>73<\/em>, 1230-1237 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2017.01.025\">10.1016\/j.tet.2017.01.025<\/a><\/p>\r\n<p>Rezankova, M.; Budka, J.; Miksatko, J.; Eigner, V.; Cisarova, I.; Curinova, P.; Lhotak, P.:<br><span class=\"cervena0\">Anion Receptors based on Intramolecularly Bridged Calix[4]arenes bearing Ureido Functions<\/span><br><em>Tetrahedron<\/em> <strong>2017<\/strong>, <em>73<\/em>, 742-749 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2016.12.054\">10.1016\/j.tet.2016.12.054<\/a><\/p>\r\n<h2><strong>2016:<\/strong><\/h2>\r\n<p>Liska, A.; Lhotak, P.; Ludvik, J.:<br><span class=\"cervena0\">Electrochemical Reduction and Intramolecular Electron Communication of Nitro Substituted Thiacalix[4]arene<\/span><br><em>Electroanalysis<\/em> <strong>2016<\/strong>, <em>28<\/em>, 2861-2865 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/elan.201600342\">10.1002\/elan.201600342<\/a><\/p>\r\n<p>Slavik, P.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">A General Method for Obtaining Calixarene Derivatives in the 1,2-Alternate Conformation<\/span><br><em>Tetrahedron<\/em> <strong>2016<\/strong>, <em>72<\/em>, 6348-6355 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2016.08.028\">10.1016\/j.tet.2016.08.028<\/a><\/p>\r\n<p>Klejch, T.; Slavicek, J.; Hudecek, O.; Eigner, V.; Gutierrez, N. A.; Curinova, P.; Lhotak, P.:<br><span class=\"cervena0\">Calix[4]arene Containing a Ureido Functionality on the Lower Rim as Highly Efficient Receptors for Anion Recognition<\/span><br><em>New J. Chem.<\/em> <strong>2016<\/strong>, <em>40<\/em>, 7935-7942 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c6nj01271j\">10.1039\/c6nj01271j<\/a><\/p>\r\n<p>Miksatko, J.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Selective Oxidation of Thiacalix[4]arene (<em>cone<\/em>) to all Corresponding Sulfoxides<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2016<\/strong>, <em>57<\/em>, 3781-3784 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2016.07.022\">10.1016\/j.tetlet.2016.07.022<\/a><\/p>\r\n<p>Slavik, P.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Shaping of Calix[4]arenes via Double Bridging of the Upper Rim<\/span><br><em>Cryst. Eng. Comm.<\/em> <strong>2016<\/strong>, <em>18<\/em>, 4964-4970 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6CE00314A\">10.1039\/C6CE00314A<\/a><\/p>\r\n<p>Botha, F.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Arylation of Thiacalix[4]arenes using Organomercurial Intermediates<\/span><br><em>New J. Chem.<\/em> <strong>2016<\/strong>, <em>40<\/em>, 1104-1110 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5NJ02427G\">10.1039\/C5NJ02427G<\/a><\/p>\r\n<p>Slavik, P.; Kohout, M.; Bohm, S.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Synthesis of Inherently Chiral Calixarenes via Direct Mercuration of the Partial Cone Conformation<\/span><br><em>Chem. Comm.<\/em> <strong>2016<\/strong>, <em>52<\/em>, 2366-2369 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5CC09388K\">10.1039\/C5CC09388K<\/a><\/p>\r\n<p>Stejskal, F.; Curinova, P.; Lhotak, P.:<br><span class=\"cervena0\">Unexpected Formation of Disulfide-based Biscalix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2016<\/strong>, <em>72<\/em>, 760-766 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2015.12.037\">10.1016\/j.tet.2015.12.037<\/a><\/p>\r\n<p>Kundrat, O.; Slavik, P.; Miksatko, J.:<br><span class=\"cervena0\">Introducing an Amine Group to Calix[5]arene: Comparison of Several Methods<\/span><br><em>Supramol. Chem.<\/em> <strong>2016<\/strong>, <em>28<\/em>, 450-454 DOI:<a href=\"http:\/\/dx.doi.org\/10.1080\/10610278.2015.1119275\">10.1080\/10610278.2015.1119275<\/a><\/p>\r\n<h2><strong>2015:<\/strong><\/h2>\r\n<p>Zajicova, M.; Eigner, V.; Budka, J.; Lhotak, P.:<br><span class=\"cervena0\">Intramolecular Bridging of Calix[4]arene Dialdoximes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2015<\/strong>, <em>56<\/em>, 5529-5532 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.08.032\">10.1016\/j.tetlet.2015.08.032<\/a><\/p>\r\n<p>Vrzal, L.; Kratochvilova-Simanova, M.; Landovsky, T.; Polivkova, K.; Budka, J.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Application of RDC Enhanced NMR Spectroscopy in Structural Analysis of Thiacalix[4]arene Derivatives<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2015<\/strong>, <em>13<\/em>, 9610-9618 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5OB01424G\">10.1039\/C5OB01424G<\/a><\/p>\r\n<p>Stejskal, F.; Eigner, V.; Dvorakova, H.; Curinova, P.; Lhotak, P.:<br><span class=\"cervena0\">Direct C-H Azidation of Calix[4]arene as a Novel Method to Access meta Substituted Derivatives<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2015<\/strong>, <em>56<\/em>, 5357-5361 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.08.002\">10.1016\/j.tetlet.2015.08.002<\/a><\/p>\r\n<p>Slavik, P.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds<\/span><br><em>Org. Lett.<\/em> <strong>2015<\/strong>, <em>17<\/em>, 2788-2791 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.5b01200\">10.1021\/acs.orglett.5b01200<\/a><\/p>\r\n<p>Liska, A.; Flidrova, K.; Lhotak, P.; Ludvik, J.:<br><span class=\"cervena0\">Influence of Structure on Electrochemical Reduction of Isomeric Mono- and Di-, Nitro- or Nitrosocalix[4]arenes<\/span><br><em>Monatshefte fuer Chemie<\/em> <strong>2015<\/strong>, <em>146<\/em>, 857-862 DOI:<a href=\"http:\/\/dx.doi.org\/10.1007\/s00706-015-1441-8\">10.1007\/s00706-015-1441-8<\/a><\/p>\r\n<p>Hucko, M.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">2,14-Dithiacalix[4]arene and its Homooxa Analogues: Synthesis and Dynamic NMR Study of Conformational Behaviour<\/span><br><em>Chem. Comm.<\/em> <strong>2015<\/strong>, <em>51<\/em>, 7051-7053 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5CC00819K\">10.1039\/C5CC00819K<\/a><\/p>\r\n<p>Spendlikova, I.; John, J.; Cuba, V.; Jirasek, J.; Lhotak, P.:<br><span class=\"cervena0\">Thiacalixarenes: Radiation Stability and Eu\/Am Extraction in Synergistic Systems with COSANs<\/span><br><em>J. Radioanalyt. Nucl. Chem.<\/em> <strong>2015<\/strong>, <em>304<\/em>, 257-262 DOI:<a href=\"http:\/\/dx.doi.org\/10.1007\/s10967-014-3694-9\">10.1007\/s10967-014-3694-9<\/a><\/p>\r\n<p>Mackova, M.; Miksatko, J.; Budka, J.; Eigner, V.; Curinova, P.; Lhotak, P.:<br><span class=\"cervena0\">Chiral Anion Recognition by a Ureido-Thiacalix[4]arene Ligand Immobilized in the <em>1,3-Alternate<\/em> Conformation<\/span><br><em>New J. Chem.<\/em> <strong>2015<\/strong>, <em>39<\/em>, 1382-1389 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C4NJ01956C\">10.1039\/C4NJ01956C<\/a><\/p>\r\n<p>Flidrova, K.; Liska, A.; Ludvik, J.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Fullerene Recognition by 5-Nitro-11,17,23,29-tetramethylcalix[5]arene<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2015<\/strong>, <em>56<\/em>, 1535-1538 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.02.016\">10.1016\/j.tetlet.2015.02.016<\/a><\/p>\r\n<p>Skacel, J.; Budka, J.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective Friedel-Crafts Acylation of Calix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2015<\/strong>, <em>71<\/em>, 1959-1965 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2015.02.021\">10.1016\/j.tet.2015.02.021<\/a><\/p>\r\n<h2><strong>2014:<\/strong><\/h2>\r\n<p>Lukasek, J.; B\u00f6hm, S.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective Halogenation of Thiacalix[4]arenes in the <em>Cone<\/em> and <em>1,3-Alternate<\/em> Conformations<\/span><br><em>Org. Lett.<\/em> <strong>2014<\/strong>, <em>16<\/em>, 5100-5103 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/ol5024536\">10.1021\/ol5024536<\/a><\/p>\r\n<p>Slavik, P.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective Alkylation of a Methylene Group via <em>meta<\/em>-bridging Calix[4]arenes<\/span><br><em>Chem. Commun.<\/em> <strong>2014<\/strong>, <em>50<\/em>, 10112-10114 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C4CC04356A\">10.1039\/C4CC04356A<\/a><\/p>\r\n<p>Liska, A.; Rosenkranz, M.; Klima, J.; Dunsch, L.; Lhotak, P., Ludvik, J.:<br><span class=\"cervena0\">Formation and Proof of Stable bi-, tri- and tetraradical Polyanions during the Electrochemical Reduction of <em>cone<\/em>-polynitrocalix[4]arenes<\/span><br><em>Electrochimica Acta<\/em> <strong>2014<\/strong>, <em>140<\/em>, 572-578 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.electacta.2014.06.042\">10.1016\/j.electacta.2014.06.042<\/a><\/p>\r\n<p>Botha, F.; B\u00f6hm, S.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Mercuration of Thiacalix[4]arenes in the <em>Cone<\/em> and <em>1,3-Alternate<\/em> Conformations<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2014<\/strong>, <em>12<\/em>, 5136-5143 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C4OB00799A\">10.1039\/C4OB00799A<\/a><\/p>\r\n<p>Vrzal, L.; Flidrova, K.; Tobrman, T.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Use of Residual Dipolar Couplings in Conformational Analysis of <em>meta<\/em>-disubstituted Calix[4]arenes<\/span><br><em>Chem. Commun.<\/em> <strong>2014<\/strong>, <em>50<\/em>, 6749-6751 DOI:<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2014\/CC\/c4cc02274b\">10.1039\/C4CC02274B<\/a><\/p>\r\n<p>Botha, F.; Budka, J.; Eigner, V.; Hudecek, O.; Vrzal, L.; Cisarova, I.; Lhotak, P.:<br><span class=\"cervena0\">Recognition of Chiral Anions using Calix[4]arene-based Ureido Receptor in the <em>1,3-Alternate<\/em> Conformation<\/span><br><em>Tetrahedron<\/em> <strong>2014<\/strong>, <em>70<\/em>, 477-483 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2013.11.030\">10.1016\/j.tet.2013.11.030<\/a><\/p>\r\n<p>Flidrova, K.; Bohm, S.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Dimercuration of Calix[4]arenes: Novel Substitution Pattern in Calixarene Chemistry<\/span><br><em>Org. Lett.<\/em> <strong>2014<\/strong>, <em>16<\/em>, 138-141 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/ol403133b\">10.1021\/ol403133b<\/a><\/p>\r\n<h2><strong>2013:<\/strong><\/h2>\r\n<p>Slavik, P.; Flidrova, K.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\"><em>Meta<\/em>-Arylation of Calixarenes using Organomercurial Chemistry<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2013<\/strong>, <em>11<\/em>, 5528-5532 DOI:<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2013\/OB\/c3ob41085d\">10.1039\/c3ob41085d<\/a><\/p>\r\n<p>Flidrova, K.; Slavik, P.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\"><em>meta<\/em>-Bridged Calix[4]arenes: A Straightforward Synthesis via Organomercurial Chemistry<\/span><br><em>Chem. Commun.<\/em> <strong>2013<\/strong>, <em>49<\/em>, 6749-6751 DOI:<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2013\/CC\/c3cc43284j\">10.1039\/c3cc43284j<\/a><\/p>\r\n<p>Holub, J.; Eigner, V.; Vrzal, L.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Calix[4]arenes with Intramolecularly Bridged <em>meta<\/em> Positions Prepared via Pd-catalysed Double C\u2013H Activation<\/span><br><em>Chem. Commun.<\/em> <strong>2013<\/strong>, <em>49<\/em>, 2798-2800 DOI:<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2013\/CC\/c3cc40655e\">10.1039\/C3CC40655E<\/a><\/p>\r\n<p>Mackova, M.; Himl, M.; Budka, J.; Pojarova, M.; Cisarova, I.; Eigner, V.; Curinova, P.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">Self-assembly of 5,11,17,23-Tetranitro-25,26,27,28-tetramethoxythiacalix[4]arene with Neutral Molecules and its Use for Anion Recognition<\/span><br><em>Tetrahedron<\/em> <strong>2013<\/strong>, <em>69<\/em>, 1397-1402 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2012.10.101\">10.1016\/j.tet.2012.10.101<\/a><\/p>\r\n<p>Hudecek, O.; Budka, J.; Dvorakova, H.; Curinova, P.; Cisarova, I.; Lhotak, P.:<br><span class=\"cervena0\">Anion Receptors based on Ureidocalix[4]arenes Immobilised in the <em>Partial cone<\/em> Conformation<\/span><br><em>New J. Chem.<\/em> <strong>2013<\/strong>, <em>37<\/em>, 220-227 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c2nj40724h\">10.1039\/c2nj40724h<\/a><\/p>\r\n<h2><strong>2012:<\/strong><\/h2>\r\n<p>Slavik, P.; Dudic, M.; Flidrova, K.; Sykora, J.; Cisarova, I.; B\u00f6hm, S.; Lhotak, P.:<br><span class=\"cervena0\">Unprecedented <em>meta<\/em>-Substitution of Calixarenes: Direct Way to Inherently Chiral Derivatives<\/span><br><em>Org. Lett.<\/em> <strong>2012<\/strong>, <em>14<\/em>, 3628-3631 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/ol301420t\">10.1021\/ol301420t<\/a><\/p>\r\n<p>Kundrat, O.; Dvorakova, H.; Bohm, S.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\"><em>S<\/em>-Alkylation of Thiacalix[4]arenes: How the Regio- and Stereoselectivities Depend on the Starting Conformation<\/span><br><em>Org. Chem.<\/em> <strong>2012<\/strong>, <em>77<\/em>, 2272-2278 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/jo202571h\">10.1021\/jo202571h<\/a><\/p>\r\n<p>Hudecek, O.; Budka, J.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective <em>ipso<\/em>-Nitration of Calix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2012<\/strong>, <em>68<\/em>, 4187-4193 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2012.03.102\">10.1016\/j.tet.2012.03.102<\/a><\/p>\r\n<p>Flidrova, K.; Tkadlecova, M.; Lang, K.; Lhotak, P.:<br><span class=\"cervena0\">Anion Recognition by Calix[4]arene\u2013based <em>p<\/em>-Nitrophenyl Amides<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2012<\/strong>, <em>53<\/em>, 678-680 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2011.11.127\">10.1016\/j.tetlet.2011.11.127<\/a><\/p>\r\n<p>Flidrova, K.; Tkadlecova, M.; Lang, K.; Lhotak, P.:<br><span class=\"cervena0\">Anion Complexation by Calix[4]arene\u2013TTF Conjugates<\/span><br><em>Dyes and Pigments<\/em> <strong>2012<\/strong>, <em>92<\/em>, 668-673 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.dyepig.2011.06.001\">10.1016\/j.dyepig.2011.06.001<\/a><\/p>\r\n<h2><strong>2011:<\/strong><\/h2>\r\n<p>Kundrat, O.; Eigner, V.; Curinova, P.; Kroupa, J.; Lhotak, P.:<br><span class=\"cervena0\">Anion-Binding by <em>meta<\/em> Ureido-Substituted Thiacalix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2011<\/strong>, <em>67<\/em>, 8367-8372 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2011.08.062\">10.1016\/j.tet.2011.08.062<\/a><\/p>\r\n<p>Kundrat, O.; Eigner, V.; Dvorakova, H.; Lhotak, P.:<br><span class=\"cervena0\">S-Alkylation of Thiacalixarenes: A Long-Neglected Possibility in the Calixarene Family<\/span><br><em>Org. Lett.<\/em> <strong>2011<\/strong>, <em>13<\/em>, 4032-4035 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/ol201546y\">10.1021\/ol201546y<\/a><\/p>\r\n<p>Hudecek, O.; Curinova, P.; Budka, J.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective Upper Rim Substitution of Calix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2011<\/strong>, <em>67<\/em>, 5213-5218 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2011.05.049\">10.1016\/j.tet.2011.05.049<\/a><\/p>\r\n<p>Mackova, M.; Himl, M.; Minarova, L.; Lang, J.; Lhotak, P.:<br><span class=\"cervena0\">Regioselective Deuteration of 25,27-Dialkoxycalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2011<\/strong>, <em>52<\/em>, 2543-2546 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2011.03.030\">10.1016\/j.tetlet.2011.03.030<\/a><\/p>\r\n<p>Lhotak P., Kundrat O.: <strong><em>Fullerene Receptors Based on Calixarene Derivatives<\/em><\/strong> in <em>Artificial Receptors for Chemical Sensors<\/em>, Mirsky V., Yatsimirsky A. (Eds.), <strong>2011<\/strong>, 249-272, Wiley-VCH Verlag, Weinheim, Germany, ISBN: 978-3-527-32357-9.<\/p>\r\n<h2><strong>2010:<\/strong><\/h2>\r\n<p>Kundrat, O.; Kroupa, J.; Bohm, S.; Budka, J.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Meta Nitration of Thiacalixarenes<\/span><br><em>J. Org. Chem.<\/em> <strong>2010<\/strong>, <em>75<\/em>, 8372-8375 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/jo1013492\">10.1021\/jo1013492<\/a><\/p>\r\n<p>Snejdarkova, M.; Poturnayova, A.; Rybar, P.; Lhotak, P.; Himl, M.; Flidrova, K.; Hianik, T.:<br><span class=\"cervena0\">High Sensitive Calixarene-Based Sensor for Detection of Dopamine by Electrochemical and Acoustic Methods<\/span><br><em>Bioelectrochemistry<\/em> <strong>2010<\/strong>, <em>80<\/em>, 55-61 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.bioelechem.2010.03.006\">10.1016\/j.bioelechem.2010.03.006<\/a><\/p>\r\n<p>Curinova, P.; Pojarova, M.; Budka, J.; Lang, K.; Stibor, I.; Lhotak, P.:<br><span class=\"cervena0\">Binding of Neutral Molecules by p-Nitrophenylureido Substituted Calix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2010<\/strong>, <em>66<\/em>, 8047-8050 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2010.08.006\">10.1016\/j.tet.2010.08.006<\/a><\/p>\r\n<p>Kriz, J.; Toman, P.; Makrlik, E.; Budka, J.; Shukla, R.; Rathore, R.:<br><span class=\"cervena0\">Cooperative Interaction of Hydronium Ion with an Ethereally Fenced Hexaarylbenzene-Based Receptor<\/span><br><em>J. Phys. Chem. A<\/em> <strong>2010<\/strong>, <em>114<\/em>, 5327-5334 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/jp101080h\">10.1021\/jp101080h<\/a><\/p>\r\n<p>Budka, J.; Eigner, V.; Holakovsky, R.; Kovaricek, P.; Louzilova, T.:<br><span class=\"cervena0\">25,26,27,28-Tetrapropoxycalix[4]arene-5,17-dicarbonitrile<\/span><br><em>Acta Crystallogr. E<\/em> <strong>2010<\/strong>, <em>66<\/em>, O419 DOI:<a href=\"http:\/\/dx.doi.org\/10.1107\/S1600536810002242\">10.1107\/S1600536810002242<\/a><\/p>\r\n<p>Van Rossom, W.; Kundrat, O.; Ngo, T. H.; Lhotak, P.; Dehaen, W.; Maes, W.:<br><span class=\"cervena0\">An oxacalix[2]arene[2]pyrimidine-bis(Zn-porphyrin) tweezer as a selective receptor towards fullerene C70<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2010<\/strong>, <em>51<\/em>, 2423-2426 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2010.02.137\">10.1016\/j.tetlet.2010.02.137<\/a><\/p>\r\n<p>Kundrat, O.; Dvorakova, H.; Eigner, V.; Lhotak, P.:<br><span class=\"cervena0\">Uncommon Regioselectivity in the Thiacalix[4]arene Series: Gross Formylation of the Cone Conformer<\/span><br><em>J. Org. Chem.<\/em> <strong>2010<\/strong>, <em>75<\/em>, 407-411 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/jo902240h\">10.1021\/jo902240h<\/a><\/p>\r\n<p>Bezouska, K. et al.:<br><span class=\"cervena0\">Carboxylated calixarenes bind strongly to CD69 and protect CD69+ killer cells from suicidal cell death induced by tumor cell surface ligands<\/span><br><em>Bioorg. Med. Chem.<\/em> <strong>2010<\/strong>, <em>18<\/em>, 1434-1440 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.bmc.2010.01.015\">10.1016\/j.bmc.2010.01.015<\/a><br><span class=\"cervena0\">This article has been retracted at the request of the authors due to data fabrication and manipulation of exptl. material by the first author.<\/span><\/p>\r\n<h2><strong>2009:<\/strong><\/h2>\r\n<p>Kundrat, O.; Dvorakova, H.; Cisarova, I.; Pojarova, M.; Lhotak, P.:<br><span class=\"cervena0\">Unusual Intramolecular Bridging Reaction in Thiacalix[4]arene Series<\/span><br><em>Org. Lett.<\/em> <strong>2009<\/strong>, <em>11<\/em>, 4188-4191 DOI: 10.1021\/ol901812m<\/p>\r\n<p>Polivkova, K.; Simanova, M.; Budka, J.; Curinova, P.; Cisarova, I.; Lhotak, P.:<br><span class=\"cervena0\">Unexpected behaviour of monospirothiacalix[4]arene under acidic conditions<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2009<\/strong> DOI: 10.1016\/j.tetlet.2009.08.105<\/p>\r\n<p>Kundrat, O.; Cisarova, I.; Bohm, S.; Pojarova, M.; Lhotak, P.:<br><span class=\"cervena0\">Uncommon Regioselectivity in Thiacalix[4]arene Formylation<\/span><br><em>J. Org. Chem.<\/em> <strong>2009<\/strong>, <em>74<\/em>, 4592-4596.<\/p>\r\n<p>Kriz, J.; Dybal, J.; Makrlik, E.; Budka, J.; Vanura, P.:<br><span class=\"cervena0\">Interaction of hydrated protons with trioctylphosphine oxide: NMR and theoretical study<\/span><br><em>J. Phys. Chem. A<\/em> <strong>2009<\/strong>, <em>113<\/em>, 5896-5905.<\/p>\r\n<p>Makrlik, E.; Vanura, P.; Budka, J.:<br><span class=\"cervena0\">On the protonation of dibenzo-18-crown-6<\/span><br><em>Monatsh. Chem.<\/em> <strong>2009<\/strong>, <em>140<\/em>, 583-585.<\/p>\r\n<p>Curinova, P.; Stibor, I.; Budka, J.; Sykora, J.; Lang, K.; Lhotak, P.:<br><span class=\"cervena0\">Anion Recognition by diureido-calix[4]arenes in the <em>1,3-alternate<\/em> conformation<\/span><br><em>New J. Chem.<\/em> <strong>2009<\/strong>, <em>33<\/em>, 612-619.<\/p>\r\n<p>Makrlik, E.; Budka, J.; Vanura, P.; Selucky, P.:<br><span class=\"cervena0\">Stability constants of some metal cation complexes of tetraphenyl <em>p-tert<\/em>-butylcalix[4]arene tetraketone in nitrobenzene saturated with water<\/span><br><em>Monatsh. Chem.<\/em> <strong>2009<\/strong>, <em>140<\/em>, 157-160.<\/p>\r\n<h2><strong>2008:<\/strong><\/h2>\r\n<p>Kriz, J.; Dybal, J.; Makrlik, E.; Budka, J.:<br><span class=\"cervena0\">Interaction of hydronium ion with dibenzo-18-crown-6: NMR, IR and theoretical study<\/span><br><em>J. Phys. Chem. A<\/em> <strong>2008<\/strong>, <em>112<\/em>, 10236-10243<\/p>\r\n<p>Kriz, J.; Dybal, J.; Budka, J.; Makrlik, E.:<br><span class=\"cervena0\">NMR and theoretical study of the kooperative interaction of hydrated proton with dibenzo-24-crown-8<\/span><br><em>Magn. Reson. Chem.<\/em> <strong>2008<\/strong>, <em>46<\/em>, 1015-1024<\/p>\r\n<p>Makrlik, E.; Budka, J.; Vanura, P.; Dybal, J.:<br><span class=\"cervena0\">Solvent extraction of univalent cations into nitrobenzene using sodium dicarbollylcobaltate and tetraphenyl p-tert-butylcalix[4]arene tetraketone<\/span><br><em>Monatsh. Chem.<\/em> <strong>2008<\/strong>, <em>139<\/em>, 1349-1351.<\/p>\r\n<p>Dybal, J.; Makrlik, E.; Vanura, P.; Budka, J.:<br><span class=\"cervena0\">DFT-calculated structure of protonated tetraphenyl p-tert-butylcalix[4]arene tetraketone<\/span><br><em>Monatsh. Chem.<\/em> <strong>2008<\/strong>, <em>139<\/em>, 1353-1355.<\/p>\r\n<p>Kriz, J.; Dybal, J.; Makrlik, E.; Budka, J.; Vanura, P.:<br><span class=\"cervena0\">Protonation of tetrapropoxy-4-tert-butylcalix[4]arene: NMR study<\/span><br><em>Supramol. Chem.<\/em> <strong>2008<\/strong>, <em>20<\/em>, 487-494.<\/p>\r\n<p>Dybal, J.; Makrlik, E.; Vanura, P.; Budka, J.:<br><span class=\"cervena0\">Protonation of 25,27-bis(1-octyloxy)-calix[4]arene-crown-6 in the 1,3-alternate conformation<\/span><br><em>Monatsh. Chem.<\/em> <strong>2008<\/strong>, <em>139<\/em>, 1175-1178.<\/p>\r\n<p>Kriz, J.; Dybal, J.; Makrlik, E.; Budka, J.:<br><span class=\"cervena0\">Cooperative interaction of butylammonium ion with <em>1,3-alternate<\/em> tetrapropoxycalix[4]arene: NMR and theoretical study<\/span><br><em>Magn. Reson. Chem.<\/em> <strong>2008<\/strong>, <em>46<\/em>, 399-407.<\/p>\r\n<p>Kriz, J.; Dybal, J.; Makrlik, E.; Budka, J.:<br><span class=\"cervena0\">Cooperative interaction of H<sub>3<\/sub>O<sup>+<\/sup> with 1,3-alternate tetrapropoxycalix[4]arene: NMR and theoretical study<\/span><br><em>Magn. Reson. Chem.<\/em> <strong>2008<\/strong>, <em>46<\/em>, 235-243.<\/p>\r\n<p>Kroupa J.; Stibor I.; Pojarova M.; Tkadlecova M.; Lhotak P.:<br><span class=\"cervena0\">Anion receptors based on ureido-substituted thiacalix[4]arenes and calix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2008<\/strong>, <em>64<\/em>, 10075-10079.<\/p>\r\n<p>Kubat P.; Lang K.; Lhotak P.; Janda P.; Sykora J.; Matejicek P.; Prochazka K.; Zelinger Z.:<br><span class=\"cervena0\">Porphyrin\/calixarene self-assemblies in aqueous solution<\/span><br><em>Photochem. Photobiol. A: Chemistry<\/em> <strong>2008<\/strong>, <em>198<\/em>, 18-25.<\/p>\r\n<p>Stibor I.; Budka J.; Michlova V.; Tkadlecova M.; Pojarova M.; Curinova P.; Lhotak P.:<br><span class=\"cervena0\">The Systematic Approach to the New Ligands for Anion Recognition Based on Ureido-calix[4]arenes<\/span><br><em>New. J. Chem.<\/em> <strong>2008<\/strong>, 32, 1597-1607.<\/p>\r\n<p>Lhotak P.; Bila A.; Budka J.; Pojarova M.; Stibor I.:<br><span class=\"cervena0\">Simple synthesis of calix[4]arenes in a <em>1,2-alternate<\/em> conformation<\/span><br><em>Chem. Commun.<\/em> <strong>2008<\/strong>, 1662-1664.<\/p>\r\n<p>Simanova M.; Dvorakova H.; Stibor I.; Pojarova M.; Lhotak P.:<br><span class=\"cervena0\">Synthesis and conformational behaviour of lower-rim tetraacetylated thiacalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2008<\/strong>, <em>49<\/em>, 1026-1029.<\/p>\r\n<p>Lang K.; Proskova P.; Kroupa J.; Moravek J.; Stibor I.; Pojarova M.; Lhotak P.:<br><span class=\"cervena0\">The synthesis and complexation of novel azosubstituted calix[4]arenes and thiacalix[4]arenes<\/span><br><em>Dyes and Pigments<\/em> <strong>2008<\/strong>, <em>77<\/em>, 646-652.<\/p>\r\n<h2><strong>2007:<\/strong><\/h2>\r\n<p>Krajewska A.; Lhotak P.; Radecka H.:<br><span class=\"cervena0\">Potentiometric Responses of Ion-Selective Electrodes Doped with Diureidocalix[4]arene towards Un-dissociated Benzoic Acid<\/span><br><em>Sensors<\/em> <strong>2007<\/strong>, <em>7<\/em>, 1655-1666.<\/p>\r\n<p>Dvorakova H.; Lang J.; Vlach J.; Sykora J.; Cajan M.; Himl M.; Pojarova M.; Stibor I.; Lhotak P.:<br><span class=\"cervena0\">Partially O-Alkylated Thiacalix[4]arenes: Synthesis, Molecular and Crystal Structures, Conformational Behaviour<\/span><br><em>J. Org. Chem.<\/em> <strong>2007<\/strong>, <em>72<\/em>, 7157-7166.<\/p>\r\n<p>Kundrat O.; Kas M.; Tkadlecova M.; Lang K.; Cvacka J.; Stibor I.; Lhotak P.:<br><span class=\"cervena0\">Thiacalix[4]arene-porphyrin conjugates with high selectivity towards fullerene C<sub>70<\/sub><\/span><br><em>Tetrahedron Lett.<\/em> <strong>2007<\/strong>, <em>48<\/em>, 6620-6623.<\/p>\r\n<p>Krenek K.; Kuldova M.; Hulikova K.; Stibor I.; Lhotak P.; Dudic M.; Budka J.; Pelantova H.; Bezouska K.; Fiserova A.; Kren V.:<br><span class=\"cervena0\"><em>N<\/em>-Acetyl-D-glucosamine substituted calix[4]arenes as stimulators of NK cell-mediated antitumor immune response<\/span><br><em>Carbohydr. Res.<\/em> <strong>2007<\/strong>, <em>342<\/em>, 1781-1792.<\/p>\r\n<p>Kas M.; Lang K.; Stibor I.; Lhotak P.:<br><span class=\"cervena0\">Novel fullerene receptors based on calixarene\u2013porphyrin conjugates<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2007<\/strong>, <em>48<\/em>, 477-481.<\/p>\r\n<p>Sykora J.; Himl M.; Stibor I.; Cisarova I.; Lhotak P.:<br><span class=\"cervena0\">Unique Self-Assembly Patterns Based on Thiacalix[4]arene-Silver Interactions<\/span><br><em>Tetrahedron<\/em> <strong>2007<\/strong>, <em>63<\/em>, 2244-2248.<\/p>\r\n<p>Budka J.; Curinova P.; Gu R.; Lhotak P.; Stibor I.; Schraml J.; Dehaen W.:<br><span class=\"cervena0\">A Novel Calix[4]arene \u2013 Dipyrrole Conjugate Designed For Complexation Of Ion Pairs<\/span><br><em>Naturforsch. B<\/em> <strong>2007<\/strong>, <em>62B<\/em>, 439-446.<\/p>\r\n<h2><strong>2006:<\/strong><\/h2>\r\n<p>Stastny V.; Stibor I.; Cisarova I.; Sykora J.; Pojarova M.; Lhotak P.:<br><span class=\"cervena0\">Synthesis of unique cage-like derivatives in a <em>1,3-alternate<\/em> conformation<\/span><br><em>J. Org. Chem.<\/em> <strong>2006<\/strong>, <em>71<\/em>, 5404-5406.<\/p>\r\n<p>Lang J.; Vagnerova K.; Czernek J.; Lhotak P.:<br><span class=\"cervena0\">Flip-flop motion of circular hydrogen bond array in thiacalix[4]arene<\/span><br><em>Supramol. Chem.<\/em> <strong>2006<\/strong>, <em>18<\/em>, 371-381.<\/p>\r\n<p>Stastny V.; Stibor I.; K\u00f6nig B.; Lhotak P.:<br><span class=\"cervena0\">Synthesis of calix[4]arene-cyclen conjugates<\/span><br><em>Tetrahedron<\/em> <strong>2006<\/strong>, <em>62<\/em>, 5748-5755.<\/p>\r\n<p>Lhotak P.; Svoboda J.; Stibor I.:<br><span class=\"cervena0\">Anion receptors based on ureido-thiacalix[4]arene<\/span><br><em>Tetrahedron<\/em> <strong>2006<\/strong>, <em>62<\/em>, 1253-1257.<\/p>\r\n<h2><strong>2005:<\/strong><\/h2>\r\n<p>Marecek V.; Janchelova H.; Stibor I.; Budka J.:<br><span class=\"cervena0\">Compact Poly-pyrrole Layers Formed at a Liquid|Liquid Interface<\/span><br><em>J. Electroanal. Chem.<\/em> <strong>2005<\/strong>, <em>575<\/em>, 293-299<\/p>\r\n<p>Gu R.; Depraetere S.; Kotek J.; Budka J.; Wagner-Wysiecka E.; Biernat J.F.; Dehaen W.:<br><span class=\"cervena0\">Anion Recognition by a-arylazo-N-confused Calix[4]pyrroles<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2005<\/strong>, <em>3<\/em>, 2921-2923<\/p>\r\n<p>Appelhans D.; Smet M.; Khimich G.; Komber H.; Voigt D.; Lhotak P.; Kuckling D.; Voit B.:<br><span class=\"cervena0\">Lysine dendrimers based on thiacalix[4]arene core moieties as molecular scaffolds for supramolecular host systems<\/span><br><em>New. J. Chem.<\/em> <strong>2005<\/strong>, <em>29<\/em>, 1386-1389.<\/p>\r\n<p>Sykora J.; Budka J.; Lhotak P.; Stibor I.; Cisarova I.:<br><span class=\"cervena0\">Two structural types of <em>1,3-alternate<\/em> tetrapropoxycalix[4]arene derivatives in the solid state<\/span><br><em>Org. Biomol. Chem.<\/em> <strong>2005<\/strong>, <em>3<\/em>, 2572-2578.<\/p>\r\n<p>Lang K.; Curinova P.; Dudic M.; Proskova P.; Stibor I.; Stastny V.; Lhotak P.:<br><span class=\"cervena0\">Unusual stoichiometry of urea-derivatized calix[4]arenes induced by anion complexation<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2005<\/strong>, <em>46<\/em>, 4469-4472.<\/p>\r\n<p>Lang J.; Deckerova V.; Czernek J.; Lhotak P.:<br><span class=\"cervena0\">Dynamics of Circular Hydrogen Bond Array in Calix[4]arene in a Non-Polar Solvent<\/span><br><em>J. Chem. Phys.<\/em> <strong>2005<\/strong>, <em>122<\/em>, 044506.<\/p>\r\n<p>Himl M.; Pojarova M.; Stibor I.; Sykora J.; Lhotak P.:<br><span class=\"cervena0\">Stereoselective alkylation of thiacalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2005<\/strong>, <em>46<\/em>, 461-464.<\/p>\r\n<h2><strong>2004:<\/strong><\/h2>\r\n<p>Zlatuskova P.; Stibor I.; Tkadlecova M.; Lhotak P.:<br><span class=\"cervena0\">Novel anion receptors based on thiacalix[4]arene derivatives<\/span><br><em>Tetrahedron<\/em> <strong>2004<\/strong>, <em>60<\/em>, 11383-11390.<\/p>\r\n<p>Appelhans D.; Stastny V.; Komber H.; Voigt D.; Voit B.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">Novel dendritic cores based on thiacalix[4]arene derivatives<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2004<\/strong>, <em>45<\/em>, 7145-7149.<\/p>\r\n<p>Lhotak P.; Stibor I.:<br><em><strong>Calixarenes and Their Analogues: Molecular Complexation<\/strong><\/em><br>in <em>Encyclopedia of Supramolecular Chemistry<\/em>, Atwood J. L., Steed J. W. (Eds.), 2004, pp. 145-152, Marcel Dekker Inc., ISBN: 0-8247-4720-8.<\/p>\r\n<p>Lhotak P.:<br><span class=\"cervena0\">Chemistry of thiacalixarenes<\/span><br><em>Eur. J. Org. Chem.<\/em> <strong>2004<\/strong>, 1675-1692.<\/p>\r\n<p>Stibor I.; Holakovsky R.; Mustafina A. R.; Lhotak P.:<br><span class=\"cervena0\">New ligands for enantioselective recognition of chiral carboxylates based on 1,1'-binaphthalene-2,2'-diamine<\/span><br><em>Collection Czech. Chem. Commun.<\/em> <strong>2004<\/strong>, <em>69<\/em>, 365-383.<\/p>\r\n<p>Stastny V.; Stibor I.; Dvorakova H.; Lhotak P.:<br><span class=\"cervena0\">Synthesis of (thia)calix[4]arene oligomers: Towards calixarene based dendrimers<\/span><br><em>Tetrahedron<\/em> <strong>2004<\/strong>, <em>60<\/em>, 3383-3391.<\/p>\r\n<p>Dudic M.; Lhotak P.; Stibor I.; Petrickova H.; Lang K.:<br><span class=\"cervena0\">(Thia)calix[4]arene-porphyrin conjugates: Novel receptors for fullerene complexation with C<sub>70<\/sub> over C<sub>60<\/sub> selectivity<\/span><br><em>New. J. Chem.<\/em> <strong>2004<\/strong>, <em>28<\/em>, 85-90.<\/p>\r\n<h2><strong>2003:<\/strong><\/h2>\r\n<p>Lhotak P.; Smejkal T.; Stibor I.; Havlicek J.; Tkadlecova M.; Petrickova H.:<br><span class=\"cervena0\">Synthesis of a deep-cavity thiacalix[4]arene<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2003<\/strong>, <em>44<\/em>, 8093-8097.<\/p>\r\n<p>Lang J.; Tosner Z.; Lhotak P.; Kowalewski J.:<br><span class=\"cervena0\">Reorientational dynamics of two isomers of thiacalix[4]arene<\/span><br><em>Magn. Reson. Chem.<\/em> <strong>2003<\/strong>, <em>41<\/em>, 819-827.<\/p>\r\n<p>Lhotak P.; Moravek J.; Smejkal T.; Stibor I.; Sykora J.:<br><span class=\"cervena0\">Stereoselective oxidation of thiacalix[4]arenes with the NaNO<sub>3<\/sub>\/CF<sub>3<\/sub>COOH system<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2003<\/strong>, <em>44<\/em>, 7333-7336.<\/p>\r\n<p>Kyrs M.; Svoboda K.; Lhotak P.; Alexova J.:<br><span class=\"cervena0\">Synergic solvent extraction of Eu, Sr and Cs into chlorobenzene solutions of the three conformers of tetrathiocalixarene and dicarbollide<\/span><br><em>Radioanal. Nucl. Chem.<\/em> <strong>2003<\/strong>, <em>258<\/em>, 497-509.<\/p>\r\n<p>Lhotak P.; Himl M.; Stibor I.; Sykora J.; Dvorakova H.; Lang J.; Petrickova H.:<br><span class=\"cervena0\">Conformational behaviour of tetramethoxy-thiacalix[4]arenes: Solution <em>versus<\/em> solid-state study<\/span><br><em>Tetrahedron<\/em> <strong>2003<\/strong>, <em>59<\/em>, 7581-7585.<\/p>\r\n<p>Lhotak P.; Zieba R.; Hromadko V.; Stibor I.; Sykora J.:<br><span class=\"cervena0\">Neutral guest complexation with calix[4]arenes preorganised by intramolecular McMurry reaction<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2003<\/strong>, <em>44<\/em>, 4519-4522.<\/p>\r\n<p>Dudic M.; Lhotak P.; Petrickova H.; Stibor I.; Lang K.; Sykora J.:<br><span class=\"cervena0\">Calixarene-based metalloporphyrins: Molecular tweezers for complexation of DABCO<\/span><br><em>Tetrahedron<\/em> <strong>2003<\/strong>, <em>59<\/em>, 2409-2415.<\/p>\r\n<p>Miyaji H.; Dudic M.; Tucker J. H. R.; Prokes I.; Light M. E.; Gelbrich T.; Hursthouse M. B.; Stibor I.; Lhotak P.; Brammer L.:<br><span class=\"cervena0\">Binding Studies on the Control of the Conformation and Self-Assembly of a Calix[4]arenedicarboxylic Acid through Hydrogen Bonding Interactions<\/span><br><em>Supramol. Chem.<\/em> <strong>2003<\/strong>, <em>15<\/em>, 385-390.<\/p>\r\n<p>Budka J.; Lhotak P.; Stibor I.; Sykora J.; Cisarova I.:<br><span class=\"cervena0\">Solid State Calix[4]arene Tubular Assemblies Based on Cation-p Interactions<\/span><br><em>Supramol. Chem.<\/em> <strong>2003<\/strong>, <em>15<\/em>, 353-357.<\/p>\r\n<p>Dudic M.; Lhotak P.; Stibor I.; Lang K.; Proskova P.:<br><span class=\"cervena0\">Calix[4]arene-porphyrin conjugates as versatile molecular receptors for anions<\/span><br><em>Org. Lett.<\/em> <strong>2003<\/strong>, <em>5<\/em>, 149-152.<\/p>\r\n<h2><strong>2002:<\/strong><\/h2>\r\n<p>Lhotak P.; Himl M.; Stibor I.; Petrickova H.:<br><span class=\"cervena0\">Alkylation of thiacalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 9621-9624.<\/p>\r\n<p>Kyrs M.; Svoboda K.; Lhotak P.; Alexova J.:<br><span class=\"cervena0\">Solvent extraction of europium from nitric acid solutions into chlorobenzene in the presence of calixarenes and dicarbollides<\/span><br><em>Radioanal. Nucl. Chem.<\/em> <strong>2002<\/strong>, <em>254<\/em>, 455-464.<\/p>\r\n<p>Cajan M.; Lhotak P.; Lang J.; Dvorakova H.; Stibor I.; Koca J.:<br><span class=\"cervena0\">The Conformational Behaviour of Thiacalix[4]arenes: The Pinched Cone \u2013 Pinched Cone Transition<\/span><br><em>J. Chem. Soc., Perkin Trans. 2<\/em> <strong>2002<\/strong>, 1922-1929.<\/p>\r\n<p>Lhotak P.; Svoboda J.; Stibor I.; Sykora J.:<br><span class=\"cervena0\">Nitration of thiacalix[4]arene derivatives<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 7413-7417.<\/p>\r\n<p>Dudic M.; Lhotak P.; Stibor I.; Dvorakova H.; Lang K.:<br><span class=\"cervena0\">Synthesis and spectroscopic properties of porphyrin-(thia)calix[4]arene conjugates<\/span><br><em>Tetrahedron<\/em> <strong>2002<\/strong>, <em>58<\/em>, 7207-7211.<\/p>\r\n<p>Stastny V.; Lhotak P.; Michlova V.; Stibor I.; Sykora J.:<br><span class=\"cervena0\">Novel biscalix[4]arene-based anion receptors<\/span><br><em>Tetrahedron<\/em> <strong>2002<\/strong>, <em>58<\/em>, 5475-5482.<\/p>\r\n<p>Gorbatchuk V. V.; Tsifarkin A. G.; Antipin I. S.; Solomonov B. N.; Konovalov A. I.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">Nonlinear Structure-Affinity Relationships for Vapor Guest Inclusion by Solid Calixarenes<\/span><br><em>Phys. Chem. B<\/em> <strong>2002<\/strong>, <em>106<\/em>, 5845-5851.<\/p>\r\n<p>Lhotak P.; Moravek J.; Stibor I.:<br><span class=\"cervena0\">Diazo coupling: An alternative method for the upper rim amination of thiacalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 3665-3668.<\/p>\r\n<p>Kren V.; Fiserova A.; Weignerova L.; Stibor I.; Halada P.; Prikrylova V.; Sedmera P.; Pospisil M.:<br><span class=\"cervena0\">Clustered ergot alkaloids modulate celol-mediated cytotoxicity<\/span><br><em>Bioorganic &amp; Medicinal Chem.<\/em> <strong>2002<\/strong>, <em>10<\/em>, 415-424.<\/p>\r\n<p>Miyaji H.; Dudic M.; Tucker J. H. R.; Prokes I.; Light M. E.; Hursthouse M. B.; Stibor I.; Lhotak P.:<br><span class=\"cervena0\">Bis(amidopyridine)-linked calix[4]arenes: a novel type of receptor for dicarboxylic acids<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 873-878.<\/p>\r\n<p>Budka J.; Lhotak P.; Stibor I.; Michlova V.; Sykora J.; Cisarova J.:<br><span class=\"cervena0\">A biscalix[4]arene-based ditopic hard\/soft receptor for K<sup>+<\/sup>\/Ag<sup>+<\/sup> complexation<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 2857-2861.<\/p>\r\n<h2><strong>2001:<\/strong><\/h2>\r\n<p>Budka J.; Lhotak P.; Michlova V.; Stibor I.:<br><span class=\"cervena0\">Urea derivatives of calix[4]arene <em>1,3-alternate<\/em>: An anion receptor with profound negative allosteric effect<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2001<\/strong>, <em>42<\/em>, 1583-1586.<\/p>\r\n<p>Lang J.; Vlach J.; Dvorakova H.; Lhotak P.; Himl M.; Hrabal R.; Stibor I.:<br><span class=\"cervena0\">Thermal isomerisation of 25,26,27,28-tetrapropoxy-2,8,14,20-tetrathiacalix[4]arene: The first isolation of all four conformers<\/span><br><em>J. Chem. Soc., Perkin Trans. 2<\/em> <strong>2001<\/strong>, <em>4<\/em>, 576-580.<\/p>\r\n<p>Lhotak P.; Dudic M.; Stibor I.; Petrickova H.; Sykora J.; Hodacova J.:<br><span class=\"cervena0\">Unprecedented formation of lactone derivatives in thiacalix[4]arene series<\/span><br><em>J. Chem. Soc., Chem. Commun.<\/em> <strong>2001<\/strong>, 8, 731-732.<\/p>\r\n<p>Lhotak P.:<br><span class=\"cervena0\">Regioselective and stereoselective oxidation of thiacalix[4]arene tetraacetate: Synthesis of all possible sulfinylcalix[4]arenes<\/span><br><em>Tetrahedron<\/em> <strong>2001<\/strong>, <em>57<\/em>, 4775-4779.<\/p>\r\n<p>Havlicek J.; Kratky R.; Ruzickova M.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">NMR study of the new chiral calix[4]arenes<\/span><br><em>J. Mol. Struct.<\/em> <strong>2001<\/strong>, <em>563<\/em>, 301-307.<\/p>\r\n<p>Stibor I.; Ruzickova M.; Kratky R.; Vindys M.; Havlicek J.; Pinkhassik E.; Lhotak P.; Mustafina A. R.; Morozova Y. E.; Kazakova E. K.; Gubskaya V. P.:<br><span class=\"cervena0\">New Calix[4]arene-based amides \u2013 their synthesis, conformation, complexation<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>2001<\/strong>, <em>66<\/em>, 641-662.<\/p>\r\n<p>Lhotak P.; Himl M.; Stibor I.; Sykora J.; Cisarova I.:<br><span class=\"cervena0\">Upper rim substitution of thiacalix[4]arene<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2001<\/strong>, <em>42<\/em>, 7107-7110.<\/p>\r\n<p>Shtarev A. B.; Pinkhassik E.; Levin M. D.; Stibor I.; Michl J.:<br><span class=\"cervena0\">Partially bridge-fluorinated dimethyl bicyclo[1.1.1]pentane-1,3-dicarboxylates: Preparation and NMR spectra<\/span><br><em>J. Am. Chem. Soc.<\/em> <strong>2001<\/strong>, <em>123<\/em>, 3484.<\/p>\r\n<p>Maeda K.; Janchelova H.; Lhotsky A.; Stibor I.; Budka J.; Marecek V.:<br><span class=\"cervena0\">Formation of a polymer layer from monomers absorbed at liquid\/liquid interface<\/span><br><em>Electroanal. Chem.<\/em> <strong>2001<\/strong>, <em>516<\/em>, 103-109.<\/p>\r\n<p>Lang K.; Kubat P.; Lhotak P.; Mosinger J.; Wagnerova D. M.:<br><span class=\"cervena0\">Photophysical Properties and Photoinduced Electron Transfer Within Host-Guest Complexes of 5,10,15,20-Tetrakis(4-N-methylpyridyl)porphyrin with Water-soluble Calixarenes and Cyclodextrins<\/span><br><em>Photochem. Photobiol.<\/em> <strong>2001<\/strong>, <em>74<\/em>, 558-565.<\/p>\r\n<h2><strong>2000:<\/strong><\/h2>\r\n<p>Budka J.; Tkadlecova M.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">Synthesis of novel calixsugars: Calix[4]arene-monosaccharide conjugates based on amide bonds<\/span><br><em>Tetrahedron<\/em> <strong>2000<\/strong>, <em>56<\/em>, 1883-1887.<\/p>\r\n<p>Lhotak P.; Kaplanek L.; Stibor I.; Lang J.; Dvorakova H.; Hrabal R.; Sykora J.:<br><span class=\"cervena0\">NMR and X-ray analysis of 25,27-dimethoxythiacalix[4]arene: Unique infinite channels in the solid state<\/span><br><em>Tetrahedron Lett.<\/em> <strong>2000<\/strong>, <em>41<\/em>, 9339-9344.<\/p>\r\n<p>Lhotak P.; Stastny V.; Zlatuskova P.; Stibor I.; Michlova V.; Tkadlecova M.; Havlicek J.; Sykora J.:<br><span class=\"cervena0\">Synthesis and 1H NMR complexation study of thiacalix[4]arene tetraacetates<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 757-771.<\/p>\r\n<p>Hodacova J.; Stibor I.:<br><span class=\"cervena0\">Synthesis of 2,2\u00b4-bipyridines with axially chiral 1,1\u00b4-binaphthalene units<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 83.<\/p>\r\n<p>Stibor I.; Holakovsky R.; Hovorka M.:<br><span class=\"cervena0\">Synthesis of new binaphthol-based tridentate ligands for enantioselective synthesis<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 805.<\/p>\r\n<p>Lellek V.; Saman D.; Holakovsky R.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">Straightforward synthesis of axially chiral 1,4-naphthodiazepine derivatives<\/span><br><em>Synlett<\/em> <strong>2000<\/strong>, <em>11<\/em>, 1616-1618.<\/p>\r\n<p>Lellek V.; Stibor I.:<br><span class=\"cervena0\">Dendrimers with inherently axially chiral units<\/span><br><em>Materials Chem.<\/em> <strong>2000<\/strong>, <em>10<\/em>, 1061.<\/p>\r\n<p>Cernovsky K.; Svoboda J.; Stibor I.; Glogarova M.; Vanek P.; Novotna V.:<br><span class=\"cervena0\">Ferroelectric liquid crystals with a fused heterocyclic core<\/span><br><em>Ferroelectrics<\/em> <strong>2000<\/strong>, <em>241<\/em>, 231.<\/p>\r\n<p>Cajan M.; Damborsky J.; Stibor I.; Koca J.:<br><span class=\"cervena0\">Stability of complexes of aromatic amides with bromide anion: Quantitative structure-property relationship<\/span><br><em>Chem. Inf., Comput. Sci.<\/em> <strong>2000<\/strong>, <em>40<\/em>, 1151.<\/p>\r\n<h2><strong>1999:<\/strong><\/h2>\r\n<p>Lang J.; Dvorakova H.; Bartosova I.; Lhotak P.; Stibor I.; Hrabal R.:<br><span class=\"cervena0\">Conformational flexibility of a novel tetraethylether of thiacalix[4]arene. A comparison with the \"classical\" methylene-bridged compounds<\/span><br><em>Tetrahedron Lett.<\/em> <strong>1999<\/strong>, <em>40<\/em>, 373-376.<\/p>\r\n<p>Dudic M.; Lhotak P.; Kral V.; Lang K.; Stibor I.:<br><span class=\"cervena0\">Synthesis of novel porphyrin-based biscalix[4]arenes<\/span><br><em>Tetrahedron Lett.<\/em> <strong>1999<\/strong>, 40, 5949-5952.<\/p>\r\n<p>Budka J.; Dudic M.; Lhotak P.; Stibor I.:<br><span class=\"cervena0\">Simple preparation of 5-hydroxy-25,26,27,28-tetraalkyloxycalix[4]arenes: Synthesis of multiple calixarenes<\/span><br><em>Tetrahedron<\/em> <strong>1999<\/strong>, <em>55<\/em>, 12647-12654.<\/p>\r\n<p>Amr A. E.; Osama I. A. E.; Attia A. E.; Stibor I.:<br><span class=\"cervena0\">Synthesis of new potential intercalators based on chiral pyridine-2,6-dicarboxamides<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 288.<\/p>\r\n<p>Matusina Z.; Olbrimkova R.; Votavova H.; Neumann J.; Hradilek M.; Soucek M.; Malon P.; Kodicek M.; Stibor I.:<br><span class=\"cervena0\">Linear heptapeptides containing DNA-intercalators. Synthesis and interaction with DNA<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 1419.<\/p>\r\n<p>Cajan M.; Stibor I.; Koca J.:<br><span class=\"cervena0\">Computational Studies on the stability of Amide - Br<sup>-<\/sup> Complexes<\/span><br><em>Phys. Chem.<\/em> <strong>1999<\/strong>, <em>103<\/em>, 3778.<\/p>\r\n<p>Vachal P.; Svoboda J.; Stibor I.; Glogarova M.:<br><span class=\"cervena0\">New heterocyclic core structure for chiral liquid crystals<\/span><br><em>Mol. Cryst. Liq. Cryst.<\/em> <strong>1999<\/strong>, <em>328<\/em>, 367.<\/p>\r\n<p>Adcock W.; Blokhin A. V.; Elsey G. M.; Head N. H.; Krstic A. R.; Levin M. D.; Michl J.; Munton J.; Pinkhasik E.; Robert M.; Sav\u00e9ant J.-M.; Shtarev A.; Stibor I.:<br><span class=\"cervena0\">Manifestation of bridghehead-brodgehead interactions in the bicyclo[1.1.1]pentane ring system<\/span><br><em>J. Org. Chem.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 2618.<\/p>\r\n<h2><strong>1998:<\/strong><\/h2>\r\n<p>Lhotak P.; Himl M.; Pakhomova S.; Stibor I.:<br><span class=\"cervena0\">Tetraalkylated 2,8,14,20-tetrathia-calix[4]arenes: Novel infinite channels in the solid state<\/span><br><em>Tetrahedron Lett.<\/em> <strong>1998<\/strong>, <em>39<\/em>, 8915-8918.<\/p>\r\n<p>Vanura P.; Stibor I.:<br><span class=\"cervena0\">Extraction of alkaline and alkaline-earth metal cations at synergistic action of bis[undecahydro[7.8]dicarbaundecaborato(2-)cobaltate(1-) and substituted calix[n]arenes in nitrobenzene<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>1998<\/strong>, <em>63<\/em>, 2009.<\/p>\r\n<p>Hovorka M.; Smiskova I.; Holakovsky R.; Beran J.; Stibor I.:<br><span class=\"cervena0\">Chiral tridentate ligands based on 3-substituted binapthols and derived complex hydrides of aluminium<\/span><br><em>Pure&amp;Appl.Chem.<\/em> <strong>1998<\/strong>, <em>70<\/em>, 415.<\/p>\r\n<p>Kaspar M.; Hamplova V.; Pakhomov S.A.; Bubnov A.M.; Giuttard F.; Sverenyak H.; Stibor I.; Vanek M.; Glogarova M.:<br><span class=\"cervena0\">New series of ferroelectric liquid crystals with four ester groups<\/span><br><em>Liquid Crystals<\/em> <strong>1998<\/strong>, <em>24<\/em>, 599-605.<\/p>\r\n<p>Kozmik V.; Lhotak P.; Odlerova Z.; Palecek J.:<br><span class=\"cervena0\">Azachalcone derivatives and their bis substituted analogs as novel antimycobacterial agents<\/span><br><em>Coll. Czech. Chem. Commun.<\/em> <strong>1998<\/strong>, <em>63<\/em>, 698-712.<\/p>\r\n<p>Pakhomov S.; Kaspar M.; Hamplova V.; Bubnov A. M.; Sverenyak H.; Glogarova M.; Stibor I.:<br><span class=\"cervena0\">Synthesis and mesomorphic properties of (S)-lactic acid derivatives containing several ester linkages in the core<\/span><br><em>Ferroelectrics<\/em> <strong>1998<\/strong>, <em>212<\/em>, 341-8.<\/p>\r\n<p>Marecek V.; Lhotsky A.; Holub K.; Stibor I.:<br><span class=\"cervena0\">Surface complex formation at the water\/1,2-dichloroethane interface<\/span><br><em>Electrochimica Acta<\/em> <strong>1998<\/strong>, <em>44<\/em>, 155-9.<\/p>\r\n<p>Pinkhassik E.; Sidorov V.; Stibor I.:<br><span class=\"cervena0\">Calix[4]arene-based receptors with hydrogen-bonding groups immersed into a large cavity<\/span><br><em>J. Org. Chem.<\/em> <strong>1998<\/strong>, <em>63<\/em>, 9644-51.<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["22327","22325"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22327":{"idvazba":"168008","nad_uzel":"136625","pod_uzel":"22327","url":"","sablona":"4","nazev":"Lhotak's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:58:00","platne_do":null,"iduzel":"22327","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"22325":{"idvazba":"168003","nad_uzel":"136611","pod_uzel":"22325","url":"","sablona":"20","nazev":"Slider","_url_prefix":null,"poradi":"4","skupina_www":"everyone","platne_od":"18.09.2015 16:26:41.264744","platne_do":null,"iduzel":"22325","obsah":"N;","class":"slider","autonomni":"0","pod_uzly":["22326","22326"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"22326":{"idvazba":"27913","nad_uzel":"22325","pod_uzel":"22326","url":"","sablona":"20","nazev":"Slide main","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.06.2026 13:44:00","platne_do":null,"iduzel":"22326","obsah":"a:12:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:11:\"head_EN.png\";s:11:\"barva_textu\";s:0:\"\";s:10:\"idattribut\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:5:\"sirka\";s:4:\"blok\";s:10:\"rozostreni\";s:1:\"1\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}}}},"136626":{"idvazba":"168059","nad_uzel":"116995","pod_uzel":"136626","url":"\/research\/menova","sablona":"1","nazev":"Menova Group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/menova}","poradi":"9","skupina_www":"everyone","platne_od":"12.05.2026 22:02:00","platne_do":null,"iduzel":"136626","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Menova Group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1157:\"<h1 style=\"text-align: center;\">Medicinal Chemistry and Glycochemistry<\/h1>\r\n<p>We work on the borders of organic, bioorganic and medicinal chemistry. We work on two main projects: ligands for the lectin receptor DC-SIGN and their use in drug targeting and agonists of muscarinic receptors. In addition, we also synthesize ligands for the visualization of G-quadruplexes.<\/p>\r\n<p>In our lab, we do mostly organic synthesis, purification of the compounds and their characterization. The evaluation of their biological activities as well as the preparation of nanoparticles are done by our collaborators.<\/p>\r\n<p>In September 2021, we became an official Max Planck Partner Group. This prestigious partnership enables us to run several projects in the field of glycochemistry.&nbsp;<\/p>\r\n<p>More details about the projects can be found in the <a href=\"https:\/\/uoch.vscht.cz\/research-groups\/menova-en\/research\" rel=\"follow\"><strong>Research<\/strong><\/a> section.<\/p>\r\n<p><img src=\"\/files\/uzel\/0136626\/0003~~MzIwMlUoT00CAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 2025 web (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"450\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["48585","136627","136628","136629","136630"],"poduzly_count":5,"poduzly_count_aut":4,"poduzly":{"poduzly_count_aut_sum":0,"48585":{"idvazba":"168019","nad_uzel":"136630","pod_uzel":"48585","url":"","sablona":"4","nazev":"Menova Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.07.2019 18:35:00","platne_do":null,"iduzel":"48585","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136627":{"idvazba":"168012","nad_uzel":"136626","pod_uzel":"136627","url":"\/research\/menova\/people_clone_13248","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/menova\/people_clone_13248}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:35:11.165713","platne_do":null,"iduzel":"136627","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:3695:\"<p><img src=\"\/images\/0!0\/uzel\/0048586\/0005~~MzIwMlUoT00CAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 2025 web (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"450\"><\/p>\r\n<table class=\"table_bezramecku\">\r\n<tbody>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">Group leader:&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">Dr. Petra M\u00e9nov\u00e1<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">Technician:<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">Kv\u011bta B\u00e1rtov\u00e1<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 157.7px;\">PhD students:<\/td>\r\n<td style=\"width: 445.3px;\">\r\n<p><\/p>\r\n<p>Fabricio Ram\u00edrez-Cort\u00e9s \u2013 fourth year Ph.D.&nbsp;<br><br><\/p>\r\n<p><\/p>\r\n<p>Rohit Chavan \u2013 fourth year Ph.D.&nbsp;<br><br><\/p>\r\n<p>Jakub D\u00e1vid Malina \u2013 fourth year Ph.D.&nbsp;<\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 157.7px;\"><\/td>\r\n<td style=\"width: 445.3px;\"><\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">Undergraduate students:&nbsp;&nbsp;&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">\r\n<p><\/p>\r\n<p>Darja Karepova \u2013 second year master studies<br><br><\/p>\r\n<p>V\u00e1clav \u0160pi\u010dka \u2013 second year master studies<\/p>\r\n<p><br>V\u00edt Novotn\u00fd \u2013 first year master studies<\/p>\r\n<p><br>Ji\u0159\u00ed Vestf\u00e1l \u2013 third year bachelor studies<\/p>\r\n<p><br>Barbora \u0160vomov\u00e1 \u2013 thirds year bachelor studies&nbsp;<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">&nbsp;<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">\r\n<p>Alumni<\/p>\r\n<p>(graduation year, degree):&nbsp; &nbsp;<\/p>\r\n<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">\r\n<p><\/p>\r\n<p>Franti\u0161ek Stara (2025, Ing.)<\/p>\r\n<p><br>Kamila Ku\u010derov\u00e1 (2025, Bc.)<\/p>\r\n<p><br>Ond\u0159ej Dan\u011bk (2024, Ing.)<\/p>\r\n<p><br>Jan Wohlgemuth (2024, Ing.)<\/p>\r\n<p><br>Maxime Thibault (2024, Ing., double degree)<\/p>\r\n<p><br>Kate\u0159ina Jochov\u00e1 (2023, Ing.)<\/p>\r\n<p><br>Vojt\u011bch Kramn\u00fd (2023, Ing.)<\/p>\r\n<p><br>Jakub Schimmer (2023, Bc.)<\/p>\r\n<p><br>Martin Broke\u0161 (2023, Bc.)<\/p>\r\n<p><br>Ji\u0159\u00ed Ledvinka (2022, Ing., double degree)<\/p>\r\n<p><br>Morgane Moinard (2022, Ing., double degree)<\/p>\r\n<p><br>Dmytro Makarov (2021, Ing.)<\/p>\r\n<p><br>Vojt\u011bch Musil (2020, Bc.)<\/p>\r\n<p><br>Romane Vizier (2020, Ing., double degree)<\/p>\r\n<p><br>Pauline Mornat (2019, Ing., double degree)&nbsp;<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"width: 157.7px; height: 19px;\">&nbsp;<\/td>\r\n<td style=\"width: 445.3px; height: 19px;\">\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<h2 style=\"text-align: center;\">2021<\/h2>\r\n<h2 style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0048586\/0006~~MzIwMlQoT00CAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 2021 web (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"450\">2019<\/h2>\r\n<h2 style=\"text-align: center;\"><img src=\"\/images\/0!0\/uzel\/0048586\/0002~~MzIwtFRwL8ovLVAoyMgvyVcwTAEA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 2019 Group photo 1d (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"600\">2017<\/h2>\r\n<p><img src=\"\/images\/0!0\/uzel\/0048586\/0008~~MzIwNFcoT00CAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 2017 web (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"450\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["48585"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"48585":{"idvazba":"168019","nad_uzel":"136630","pod_uzel":"48585","url":"","sablona":"4","nazev":"Menova Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.07.2019 18:35:00","platne_do":null,"iduzel":"48585","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136628":{"idvazba":"168014","nad_uzel":"136626","pod_uzel":"136628","url":"\/research\/menova\/research_clone_44498","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/menova\/research_clone_44498}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:35:11.254559","platne_do":null,"iduzel":"136628","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:8215:\"<h2><strong>Projects<\/strong><\/h2>\r\n<ul>\r\n<li><a href=\"#ligands\">Synthesis of ligands for the lecitin receptor DC-SIGN<\/a><\/li>\r\n<li><a href=\"#agonists\">Synthesis of&nbsp; muscarinic receptor agonists<\/a><\/li>\r\n<li><a href=\"#hepatitis\" rel=\"follow\"><\/a><a href=\"#visualization\" rel=\"follow\">Synthesis of ligands for G-quadruplex visualization<\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<h2><a id=\"ligands\"><\/a>Synthesis of ligands for the lectin receptor DC-SIGN&nbsp;<\/h2>\r\n<p>DC-SIGN is a C-type lectin receptor found on the surface of immune cells, particularly dendritic cells and macrophages. The natural ligands of the DC-SIGN receptor are oligo- and polysaccharides rich in mannose and fucose.<\/p>\r\n<p>One of the main functions of the DC-SIGN receptor is the recognition of carbohydrates present on the surface of various pathogens: viruses (e.g., HIV, Ebola, SARS-CoV-2), bacteria (M. tuberculosis, S. pneumoniae), fungi (C. albicans), and parasites (Leishmania). Upon pathogen binding, the pathogen is internalized into the dendritic cell, triggering an immune response. However, some pathogens (e.g., HIV) exploit the interaction with the DC-SIGN receptor to facilitate their spread throughout the host organism.<\/p>\r\n<p>In addition, DC-SIGN can transmit modulatory signals that either stimulate or suppress the immune response, depending on the type of bound ligand. It also plays a role in cell adhesion.<\/p>\r\n<p>Ligands that bind selectively to the DC-SIGN receptor could have several practical medical applications:<\/p>\r\n<p>1. <strong>Targeted drug<\/strong> delivery to dendritic cells: Ligands that selectively interact with the DC-SIGN receptor can be used for the targeted delivery of siRNA, antigens, or immunomodulators via liposomes, dendrimers, or nanoparticles.<\/p>\r\n<p>2. <strong>Immunotherapy: <\/strong>Targeting dendritic cells can help enhance anti-tumour immunity. Nanoparticles modified with a specific antigen could be used to \"train\" dendritic cells to recognize that antigen.<\/p>\r\n<p>3. <strong>Antimicrobial agents:<\/strong> Selective inhibition of the DC-SIGN receptor may allow modulation of the immune response at early stages of infection and open the door to a new class of drugs for treating these diseases.<\/p>\r\n<p>The carbohydrate-binding site of the DC-SIGN receptor is rather shallow and hydrophilic, which makes it a less promising target in medicinal chemistry. However, recent studies have shown that in addition to its primary carbohydrate-binding site, DC-SIGN also possesses several secondary binding sites that are accessible to small organic molecules (Figure 1).&nbsp;<\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0048587\/0003~~MzCMd3EO9nT3AwA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \" width=\"524\" height=\"250\"><\/p>\r\n<p style=\"text-align: center;\"><strong>Figure 1.<\/strong> DC-SIGN receptor, primary carbohydrate binding site (yellow) and secondary binding sites I\u2013V. Picture taken from Aretz, J. et al.: <em>Angew. Chem. Int. Ed.<\/em> <strong>2017<\/strong>, <em>56<\/em>, 7292\u20137296.<\/p>\r\n<p>&nbsp;Our main goal is the synthesis of new DC-SIGN receptor ligands that exhibit high selectivity and favourable drug-like properties. We are preparing several types of ligands:<\/p>\r\n<p>* Carbohydrate-based glycomimetics \u2013 compounds based on D-mannose or L-fucose, carrying substituents that interact either with the surroundings of the carbohydrate-binding site or with a secondary binding site (Figure 2a).<\/p>\r\n<p>* Allosteric ligands \u2013 non-carbohydrate compounds that interact with secondary binding sites and, through their binding, modulate the interaction of carbohydrates with the primary carbohydrate-binding site (Figure 2b). The synthesis of these compounds follows a fragment-based approach.&nbsp;<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0048587\/0002~~MzCKDy4pKs0uKS2qBAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"195\"><\/p>\r\n<p style=\"text-align: center;\"><strong>Figure 2.<\/strong> Overview of the synthesized DC-SIGN ligands. a) DC-SIGN inhibitors based on D-mannose and l-fucose; b) non-carbohydrate inhibitors binding to the secondary binding sites.<\/p>\r\n<p>&nbsp;We collaborate on the project with the group of Prof. Christoph Rademacher at the University of Vienna. In his laboratory, compound affinity testing and nanoparticle formulation for targeted delivery are carried out.&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<h2><strong><a id=\"agonists\"><\/a>Synthesis of muscarinic receptor agonists&nbsp;<\/strong><\/h2>\r\n<p>Muscarinic acetylcholine receptors are G protein-coupled receptors that play a key role in many signaling pathways throughout the human body. The five known types of muscarinic receptors (M1\u2013M5) are widely expressed in both the central and peripheral nervous systems. Each subtype can be involved in maintaining various physiological functions depending on the tissue. Achieving selectivity for a specific receptor subtype and signalling pathway is crucial in developing muscarinic receptor-targeted drugs in order to minimize potential side effects.<\/p>\r\n<p>In 2020, a ligand based on a tetrahydropyridinium scaffold (Figure 3a) was discovered by Dr. Jakub\u00edk\u2019s research group. This compound, which now serves as the lead structure for our project, showed selectivity for M2 muscarinic receptors and demonstrated so-called signalling bias toward the Gi\/o pathway across all muscarinic receptor subtypes.<\/p>\r\n<p>In this project, we focus on the synthesis of muscarinic receptor agonists based on the tetrahydropyridine scaffold, which hold potential for the treatment of neuropathic pain. The synthetic part of the project includes three main goals:<\/p>\r\n<p>* Synthesis of analogues of our lead compound to study structure\u2013activity relationships (SAR).<\/p>\r\n<p>* Synthesis of bitopic ligands that incorporate both an orthosteric ligand (lead structure) and an allosteric ligand to enhance receptor affinity (Figure 3b).<\/p>\r\n<p>* Synthesis of novel ligand types predicted using computer modelling techniques.&nbsp;<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0048587\/0006~~MzCODy4pKs0uKS2qVPBVKEpNTi0oyS-qBAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 03_Struktury M receptory (jpg) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"450\" height=\"101\"><\/p>\r\n<p style=\"text-align: center;\"><strong>Figure 3.&nbsp;<\/strong>Examples of synthesized ligands for muscarinic receptors. a) Lead structure; b) example of a bitopic ligand.&nbsp;<\/p>\r\n<p>We collaborate on this project with Dr. Jan Jakub\u00edk\u2019s group at the Institute of Physiology of the Czech Academy of Sciences. In his laboratory, the affinity and selectivity of the compounds are tested.&nbsp;<\/p>\r\n<p>&nbsp;<\/p>\r\n<h2><strong><a id=\"visualization\"><\/a>Synthesis of ligands for G-quadruplex visualization<\/strong><\/h2>\r\n<p>We focus on synthesizing ligands for the visualization of G-quadruplexes. Our goal is to develop twice-as-smart fluorescent probes that function both as smart G-quadruplex ligands (i.e., they are formed only in the presence of a natural G-quadruplex) and as smart fluorescent probes (i.e., they fluoresce only in the presence of their target, the G-quadruplex).<\/p>\r\n<p>The first compound in this series (N-TASQ), synthesized by our collaborating group, was used for the very first visualization of G-quadruplexes in living human cells (Figure 4), and has since found<\/p>\r\n<p>applications in oncology and neurology. Our aim is to prepare N-TASQ-related compounds and attempt to improve their properties.&nbsp;<\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0048587\/0004~~MzCN9wtxDA4EAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 05_NTASQ (jpg) \u2192 (origin\u00e1l)\" width=\"600\" height=\"182\"><\/p>\r\n<p style=\"text-align: center;\"><strong>Figure 5<\/strong>. Twice-as-smart probes for the visualization of G-quadruplex. Picture taken from Laguerre, A. et al.: <em>J. Am. Chem. Soc.<\/em> <strong>2015<\/strong>, <em>137<\/em>, 8521\u20138525.<\/p>\r\n<p>&nbsp;We collaborate on this project with Dr. David Monchaud\u2019s group at ICMUB CNRS in Dijon, France. His laboratory conducts studies of the prepared compounds using biophysical methods.&nbsp;<\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["48585"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"48585":{"idvazba":"168019","nad_uzel":"136630","pod_uzel":"48585","url":"","sablona":"4","nazev":"Menova Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.07.2019 18:35:00","platne_do":null,"iduzel":"48585","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136629":{"idvazba":"168016","nad_uzel":"136626","pod_uzel":"136629","url":"\/research\/menova\/teaching_clone_72317","sablona":"1","nazev":"Teaching","_url_prefix":"{\/\/uoch.vscht.cz\/research\/menova\/teaching_clone_72317}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:35:11.2844","platne_do":null,"iduzel":"136629","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Teaching\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:378:\"<p>Dr. M\u00e9nov\u00e1:<\/p>\r\n<ul>\r\n<li>Medicinal chemistry (ENG)<\/li>\r\n<li>Organic chemistry: laboratory I (ENG)<\/li>\r\n<li>Z\u00e1klady farmakochemie (Fundamentals of chemistry of pharmaceuticals, CZ)<\/li>\r\n<li>Organick\u00e1 chemie A, B \u2013 semin\u00e1\u0159 (Organic chemistry A, B \u2013 seminar, CZ)<\/li>\r\n<li>Laborato\u0159 organick\u00e9 chemie I, II (Laboratory of organic chemistry I, II, CZ)<\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["48585"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"48585":{"idvazba":"168019","nad_uzel":"136630","pod_uzel":"48585","url":"","sablona":"4","nazev":"Menova Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.07.2019 18:35:00","platne_do":null,"iduzel":"48585","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136630":{"idvazba":"168018","nad_uzel":"136626","pod_uzel":"136630","url":"\/research\/menova\/publications_clone_36109","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/menova\/publications_clone_36109}","poradi":"4","skupina_www":"everyone","platne_od":"12.05.2026 21:35:11.310593","platne_do":null,"iduzel":"136630","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:13784:\"<p><strong>Papers (since the establishment of the group)&nbsp;<\/strong><\/p>\r\n<ol start=\"133\">\r\n<li>R. Chavan, M. Besch, J. Lef\u00e8bre, C. Rademacher, P. M\u00e9nov\u00e1*: Aryl fucosides: synthesis and evaluation of their binding affinity towards the DC-SIGN receptor.&nbsp;<em>Org. Bioorg. Chem.<\/em> <strong>2025<\/strong>, Advance Article. <a href=\"https:\/\/doi.org\/10.1039\/D5OB00472A\">https:\/\/doi.org\/10.1039\/D5OB00472A<\/a><br><br><\/li>\r\n<li>R. Chavan, J. Lefebre, K. Jochov\u00e1, H. Dvo\u0159\u00e1kov\u00e1, C. Rademacher, P. M\u00e9nov\u00e1*: Fucosyl glycosides for DC-SIGN targeting: Fucosylation strategies, synthesis and binding studies of model compounds.&nbsp;<em>Bioorg. Med. Chem.<\/em> <strong>2025<\/strong>,<em> 123<\/em>, 118164. <a href=\"https:\/\/doi.org\/10.1016\/j.bmc.2025.118164\">https:\/\/doi.org\/10.1016\/j.bmc.2025.118164<\/a><br><br><\/li>\r\n<li>J. Ledvinka, F. Rota Sperti, G. Paragi, M. Pirrotta, N. Ch\u00e9ron, I. E. Valverde, P. Menova*, D. Monchaud: Fluorescence Detection of DNA\/RNA G-Quadruplexes (G4s) by Twice-as-Smart Ligands.&nbsp;<em>ChemMedChem<\/em> <strong>2025<\/strong>, e202400829. <a href=\"https:\/\/doi.org\/10.1002\/cmdc.202400829\">https:\/\/doi.org\/10.1002\/cmdc.202400829<\/a><br><br><\/li>\r\n<li>F. Ram\u00edrez-Cort\u00e9s, P. M\u00e9nov\u00e1*: Hepatocyte targeting via the asialoglycoprotein receptor.&nbsp;<em>RSC Med. Chem<\/em>. <strong>2025<\/strong>, <em>16<\/em>, 525\u2013544. <a href=\"https:\/\/doi.org\/10.1039\/D4MD00652F\">https:\/\/doi.org\/10.1039\/D4MD00652F<\/a><br><br><\/li>\r\n<li>S. Leusmann, P. M\u00e9nov\u00e1, E. Shanin, A. Titz, C. Rademacher: Glycomimetics for the inhibition and modulation of lectins.&nbsp;<em>Chem. Soc. Rev.<\/em> <strong>2023<\/strong>, <em>52<\/em>, 3663\u20133740. <a href=\"https:\/\/doi.org\/10.1039\/D2CS00954D\">https:\/\/doi.org\/10.1039\/D2CS00954D<\/a>.<br><br><\/li>\r\n<li>H. Zhang, O. Dan\u011bk, D. Makarov, S. R\u00e1dl, D. Kim, J. Ledvinka, K. Vychodilov\u00e1, J. Hlav\u00e1\u010d, J. Lef\u00e8bre, M. Denis, C. Rademacher, P. M\u00e9nov\u00e1*: Drug-like Inhibitors of DC-SIGN Based on a Quinolone Scaffold,&nbsp;<em>ACS Med. Chem. Lett.<\/em> <strong>2022<\/strong>, <em>13<\/em>, 935\u2013942. <a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.2c00067\">https:\/\/doi.org\/10.1021\/acsmedchemlett.2c00067<\/a>.<br><br><\/li>\r\n<li>M\u00e9nov\u00e1: ASGPR a DC-SIGN: C-lektinov\u00e9 receptory se slibn\u00fdm potenci\u00e1lem v medicin\u00e1ln\u00ed chemii.&nbsp;<em>Chem. Listy <\/em><strong>2021<\/strong>, <em>115<\/em>, 126\u2013133.<\/li>\r\n<\/ol>\r\n<p><strong>&nbsp;<\/strong><strong>Previous papers by Petra M\u00e9nov\u00e1, written before the group was etablished&nbsp;<\/strong><\/p>\r\n<ol>\r\n<li>A. Golczak, M. Insi\u0144ska-Rak, A. Davoudpour, D. H. Saeed, P. M\u00e9nov\u00e1, V. Mojr, R. Cibulka, I. Khmelinskii, L. Mr\u00f3wczy\u0144ska, M. Sikorski: Photophysical properties of alloxazine derivatives with extended aromaticity \u2013 Potential redox-sensitive fluorescent probe,&nbsp;<em>Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy<\/em> <strong>2022<\/strong>, <em>272<\/em>, 120985. <a href=\"https:\/\/doi.org\/10.1016\/j.saa.2022.120985\">https:\/\/doi.org\/10.1016\/j.saa.2022.120985<\/a>.<br><br><\/li>\r\n<li>P. Kaplonek, L. Yao, K. Reppe, F. Vo\u00df, T. Kohler, F. Ebner, A. Sch\u00e4fer, U. Blohm, P. Priegue, M. Br\u00e4utigam, C. L. Pereira, S. G. Parameswarappa, M. Emmadi, P. M\u00e9nov\u00e1, M. Witzenrath, S. Hammerschmidt, S. Hartmann, L. E. Sander, P. H. Seeberger: A semisynthetic glycoconjugate provides expanded cross-serotype protection against Streptococcus pneumoniae,&nbsp;<em>Vaccine <\/em><strong>2022<\/strong>, <em>40 (7)<\/em>, 1038\u20131046. <a href=\"https:\/\/doi.org\/10.1016\/j.vaccine.2021.12.068\">https:\/\/doi.org\/10.1016\/j.vaccine.2021.12.068<\/a>.<br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, M. Sella, K. Sellrie, C. Pereira, P. H. Seeberger: Identification of the minimal glycotope of Streptococcus pneumoniae 7F capsular polysaccharide using synthetic oligosaccharides,<em> Chem. Eur. J. <\/em><strong>2018<\/strong>, <em>24<\/em>, 4181\u20134187. <a href=\"https:\/\/doi.org\/10.1002\/chem.201705379\">https:\/\/doi.org\/10.1002\/chem.201705379<\/a><br><br><\/li>\r\n<li>S. G. Parameswarappa, K. Reppe, A. Geissner, P. M\u00e9nov\u00e1, S. Govindan, A. D. J. Calow, A. Wahlbrink, M. W. Weishaupt, B. P. Monnanda, R. L. Bell, L.-A. Pirofski, N. Suttorp, L. E. Sander, M. Witzenrath, C. L. Pereira, C. Anish, P. H. Seeberger: A semi-synthetic oligosaccharide conjugate vaccine candidate confers protection against Streptococcus pneumoniae serotype 3 infection,&nbsp;<em>Cell Chem. Biol. <\/em><strong>2016<\/strong>, <em>23<\/em>, 1407\u20131416. <a href=\"https:\/\/doi.org\/10.1016\/j.chembiol.2016.09.016\">https:\/\/doi.org\/10.1016\/j.chembiol.2016.09.016<\/a><br><br><\/li>\r\n<li>D. Hockov\u00e1, \u0160. Rosenbergov\u00e1, P. M\u00e9nov\u00e1, O. P\u00e1v, R. Pohl, P. Nov\u00e1k, I. Rosenberg: N-Branched acyclic nucleoside phosphonates as monomers for the synthesis of modified oligonucleotides,&nbsp;<em>Org. Biomol. Chem.<\/em> <strong>2015<\/strong>, <em>13<\/em>, 4449\u20134458. <a href=\"https:\/\/doi.org\/10.1039\/C4OB02265C\">https:\/\/doi.org\/10.1039\/C4OB02265C<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, D. Dziuba, P. G\u00fcixens-Gallardo, P. Jurkiewicz, M. Hof, M. Hocek: Fluorescence Quenching in Oligonucleotides Containing 7-Substituted 7-Deazaguanine Bases Prepared by the Nicking Enzyme Amplification Reaction,&nbsp;<em>Bioconjugate Chem.<\/em> <strong>2015<\/strong>,<em> 26<\/em>, 361\u2013366. <a href=\"https:\/\/doi.org\/10.1021\/acs.bioconjchem.5b00006\">https:\/\/doi.org\/10.1021\/acs.bioconjchem.5b00006<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, H. Dvo\u0159\u00e1kov\u00e1, V. Eigner, J. Ludv\u00edk, R. Cibulka: Electron-deficient alloxazinium salts: efficient organocatalysts of mild and chemoselective sulfoxidations with hydrogen peroxide,&nbsp;<em>Adv. Synth. Catal. <\/em><strong>2013<\/strong>, <em>355<\/em>, 3451\u20133462. <a href=\"https:\/\/doi.org\/10.1002\/adsc.201300617\">https:\/\/doi.org\/10.1002\/adsc.201300617<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, V. Raindlov\u00e1, M. Hocek: Scope and Limitations of the Nicking Enzyme Amplification Reaction for the Synthesis of Base-Modified Oligonucleotides and Primers for PCR,&nbsp;<em>Bioconjugate Chem.<\/em> <strong>2013,<\/strong> <em>24<\/em>, 1081\u20131093. <a href=\"https:\/\/doi.org\/10.1021\/bc400149q\">https:\/\/doi.org\/10.1021\/bc400149q<\/a><br><br><\/li>\r\n<li>P. Perl\u00edkov\u00e1, L. Eberlin, P. M\u00e9nov\u00e1, V. Raindlov\u00e1, L. Slav\u011bt\u00ednsk\u00e1, E. Tlou\u0161\u0165ov\u00e1, G. Bahador, Y.-J. Lee, M. Hocek: Synthesis and Cytostatic and Antiviral Activities of 2\u2019-Deoxy-2\u2019,2\u2019-difluororibo- and 2\u2019-Deoxy-2\u2019-fluororibonucleosides Derived from 7-(Het)aryl-7-deazaadenines,&nbsp;<em>ChemMedChem<\/em> <strong>2013<\/strong>, <em>8<\/em>, 832\u2013846. <a href=\"https:\/\/doi.org\/10.1002\/cmdc.201300047\">https:\/\/doi.org\/10.1002\/cmdc.201300047<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, H. Cahov\u00e1, M. Plucnara, L. Havran, M. Fojta, M. Hocek: Polymerase synthesis of oligonucleotides containing a single chemically modified nucleobase for site-specific redox labelling, &nbsp;2<em>Chem. Commun. <\/em><strong>2013<\/strong>, <em>49<\/em>, 4652\u20134654. <a href=\"https:\/\/doi.org\/10.1039\/C3CC41438H\">https:\/\/doi.org\/10.1039\/C3CC41438H<\/a><br><br><\/li>\r\n<li>J. Riedl, P. M\u00e9nov\u00e1, R. Pohl, P. Ors\u00e1g, M. Fojta, M. Hocek: GFP-like fluorophores as DNA labels for studying&nbsp; &nbsp; &nbsp;DNA\u2013protein interactions, <em>J. Org. Chem.<\/em> <strong>2012<\/strong>, <em>77<\/em>, 8287\u20138293. <a href=\"https:\/\/doi.org\/10.1021\/jo301684b\">https:\/\/doi.org\/10.1021\/jo301684b<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, R. Cibulka: Insight into the catalytic activity of alloxazinium and isoalloxazinium salts in the oxidations of sulfides and amines with hydrogen peroxide,&nbsp;<em>J. Mol. Catal. A\u2013Chem<\/em>. <strong>2012<\/strong>, 363-364, 362\u2013370. <a href=\"https:\/\/doi.org\/10.1016\/j.molcata.2012.07.012\">https:\/\/doi.org\/10.1016\/j.molcata.2012.07.012<\/a><\/li>\r\n<li>P. M\u00e9nov\u00e1, M. Hocek: Preparation of short cytosine-modified oligonucleotides by nicking enzyme amplification reaction,&nbsp;<em>Chem. Commun. <\/em><strong>2012<\/strong>, <em>48<\/em>, 6921\u20136923. <a href=\"https:\/\/doi.org\/10.1039\/C2CC32930A\">https:\/\/doi.org\/10.1039\/C2CC32930A<\/a><br><br><\/li>\r\n<li>M. Pluncara, H. Pivo\u0148kov\u00e1, L. Havran, M. Hocek, P. M\u00e9nov\u00e1, H. Cahov\u00e1, J. Balintov\u00e1, M. Fojta: Site-specific labeling of nucleotides in DNA strand for possible usage in electrochemical DNA-sensors,&nbsp;<em>FEBS J.<\/em> <strong>2012<\/strong>,<em> 279<\/em>, 571\u2013572.<br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, V. Eigner, J. \u010cejka, H. Dvo\u0159\u00e1kov\u00e1, M. \u0160anda, R. Cibulka: Synthesis and structural studies of flavin and alloxazine adducts with O-nucleophiles,&nbsp;<em>J. Mol. Struct. <\/em><strong>2011<\/strong>, <em>1004<\/em>, 178\u2013187. <a href=\"https:\/\/doi.org\/10.1016\/j.molstruc.2011.08.002\">https:\/\/doi.org\/10.1016\/j.molstruc.2011.08.002<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, F. Kafka, H. Dvo\u0159\u00e1kov\u00e1, S. Gunnoo, M. \u0160anda, R. Cibulka: Pyrazinium salts as efficient organocatalysts of mild oxidations with hydrogen peroxide,<em> Adv. Synth. Catal. <\/em><strong>2011<\/strong>, <em>353<\/em>, 865\u2013870. <a href=\"https:\/\/doi.org\/10.1002\/adsc.201000906\">https:\/\/doi.org\/10.1002\/adsc.201000906<\/a><br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, V. Eigner, R. Cibulka, J. \u010cejka, H. Dvo\u0159\u00e1kov\u00e1: 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione,&nbsp;<em>Acta Cryst. E<\/em> <strong>2009<\/strong>, <em>E65<\/em>, o1536\u2013o1537. <a href=\"https:\/\/doi.org\/10.1107\/S1600536809020856\">https:\/\/doi.org\/10.1107\/S1600536809020856<\/a><br><br><\/li>\r\n<li>R. Cibulka, L. Baxov\u00e1, H. Dvo\u0159\u00e1kov\u00e1, F. Hampl, P. M\u00e9nov\u00e1, V. Mojr, B. Plancq, S. Sayin: Catalytic effect of alloxazinium and isoalloxazinium salts on oxidation of sulfides with hydrogen peroxide in micellar media, Collect. Czech.&nbsp;<em>Chem. Commun. <\/em><strong>2009<\/strong>, <em>74<\/em>, 973\u2013993. https:\/\/doi.org\/10.1135\/cccc2009030&nbsp;<\/li>\r\n<\/ol>\r\n<p><strong><\/strong><\/p>\r\n<p><em>Patents&nbsp;<\/em><\/p>\r\n<ol>\r\n<li>P. Seeberger, C. L. Pereira, S. Parameswarappa, A. Calow, P. M\u00e9nov\u00e1, S. Govindan: Improved preparation of vaccines against Streptococcus pneumoniae type 3, EP3231810A1, WO2017178664-A1, EP3292131-A1.<br><br><\/li>\r\n<li>P. Seeberger, C. L. Pereira, M. Emmadi, S. Parameswarappa, A. Calow, P. M\u00e9nov\u00e1, M. Lisboa, Ch. Martin, B. Schumann, F. Xu, N. Khan, P. Kaplonek, L. Lykke: Pneumococcal oligosaccharide-protein conjugate composition, WO2017220753, EP16179133.0.<\/li>\r\n<\/ol>\r\n<p><strong><\/strong><\/p>\r\n<p><em>Books and book chapters&nbsp;<\/em><\/p>\r\n<ol>\r\n<li>P. M\u00e9nov\u00e1, F. Hampl: Z\u00e1klady farmakochemie. V\u0160CHT Praha <strong>2022<\/strong>. ISBN 978-80-7592-119-2.<br><br><\/li>\r\n<li>P. Holzhauser, R. Matu\u0161ka, P. M\u00e9nov\u00e1: Pou\u017eit\u00ed chemick\u00fdch l\u00e1tek ve v\u00fduce a p\u0159i volno\u010dasov\u00fdch aktivit\u00e1ch \u017e\u00e1k\u016f. <em>Czech Chem. Soc. Symp. Ser. <\/em><strong>2019<\/strong>, <em>17<\/em>, 87\u2013122. ISBN 2336-7202.<br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1, H. Cahov\u00e1, M. Vr\u00e1bel, M. Hocek: Synthesis of Base-Modified dNTPs Through Cross-Coupling Reactions and Their Polymerase Incorporation to DNA. In: Shank N. (eds) Non-Natural Nucleic Acids. Methods in Molecular Biology, <strong>2019<\/strong>, <em>1973<\/em>, 39\u201357. Humana Press, New York, NY. Print ISBN 978-1-4939-9215-7, online ISBN 978-1-4939-9216-4.<br><br><\/li>\r\n<li>P. M\u00e9nov\u00e1: The IChO Theoretical Exam. In: F. M. Fung, I\u2013J. Chang (eds): 10 Things You Must Know about International Chemistry Olympiad: A Guide to the IChO Competition,&nbsp;<strong>2019<\/strong>, 29\u201335. Chang-Xin Cultural &amp; Creative Marketing. ISBN 978-986-97513-5-3.&nbsp;<\/li>\r\n<\/ol>\r\n<p><strong><br><\/strong><\/p>\r\n<p><strong>Bachelor theses<\/strong><\/p>\r\n<ol>\r\n<li>Novotn\u00fd V\u00edt: Synthesis of a library of chromones and evaluation of their affinity for DC-SIGN receptor&nbsp; &nbsp; &nbsp; &nbsp;(2025)<br>&nbsp;<\/li>\r\n<li>Ku\u010derov\u00e1 Kamila: Synthesis of M2-selective muscarinic receptor agonists and evaluation of their&nbsp; &nbsp;&nbsp; &nbsp; biological aktivity (2025)<br><br><\/li>\r\n<li>Schimmer Jakub: Diaryl mannosides and their binding affinity for DC-SIGN receptor (2023)<br><br><\/li>\r\n<li>Broke\u0161 Martin: Quinoxalinone-based DC-SIGN inhibitors (2023)<br><br><\/li>\r\n<li>Dan\u011bk Ond\u0159ej: Synthesis of quinolone-based DC-SIGN inhibitors (2022)<br><br><\/li>\r\n<li>Wohlgemuth Jan: Synthesis of 2-phenylsulfonyacrylates as potential inhibitors of DC-SIGN receptor (2022)<br><br><\/li>\r\n<li>Jochov\u00e1 Kate\u0159ina: Modified nanoparticles for DC-SIGN targeting (2021)<br><br><\/li>\r\n<li>Ledvinka Ji\u0159\u00ed: Synthesis of mannose-based DC-SIGN antagonists (2020)<br><br><\/li>\r\n<li>Musil Vojt\u011bch: Synthesis of quinoxalinone-based inhibitors of DC-SIGN receptor (2020)<br><br><\/li>\r\n<li>Wohlr\u00e1bov\u00e1 Lucie: Chelating lipids for optical quantum nanosensors (2019)<br><br><\/li>\r\n<li>Makarov Dmytro: Synt\u00e9za substituovan\u00fdch chinolon\u016f jako potenci\u00e1ln\u00edch inhibitor\u016f DC-SIGN receptoru (2018)&nbsp;<\/li>\r\n<\/ol>\r\n<p><\/p>\r\n<p>&nbsp;<\/p>\r\n<p><strong>Master theses<\/strong><\/p>\r\n<ol>\r\n<li>Karepova Darja: Synthesis of DC-SIGN ligands based on arylsulfonyl acrylate (2025)<br><br><\/li>\r\n<li>Stara Franti\u0161ek: Synthesis and evaluation of hydroxyquinolones for the treatment of skin diseases (2025)<br><br><\/li>\r\n<li>Wohlgemuth Jan: Synthesis of ligands for DC-SIGN receptor (2024)<br><br><\/li>\r\n<li>Dan\u011bk Ond\u0159ej: Synthesis of novel M2-selective muscarinic receptor agonists (2024)<br><br><\/li>\r\n<li>Kramn\u00fd Vojt\u011bch: Small-molecule ligands for DC-SIGN receptor (2023)<br><br><\/li>\r\n<li>Jochov\u00e1 Kate\u0159ina: Ligands and nanoparticles for DC-SIGN targeting (2023)<br><br><\/li>\r\n<li>Ledvinka Ji\u0159\u00ed: G-quadruplex (G4) smart probes to investigate G4s cellular functions (2022)<br><br><\/li>\r\n<li>Makarov Dmytro: Synthesis of quinolone-based inhibitors of DC-SIGN receptor (2020)<br><br><\/li>\r\n<li>Mornat Pauline: Synthesis of mannose-based DC-SIGN inhibitors bearing fluorinated arene moiety (2019)&nbsp;<\/li>\r\n<\/ol>\r\n<p><\/p>\r\n<p><strong><br>Doctoral theses&nbsp;<\/strong><\/p>\r\n<ol>\r\n<li>Chavan Rohit<br><br><\/li>\r\n<li>Ram\u00edrez-Cort\u00e9s Fabricio&nbsp;<\/li>\r\n<\/ol>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["48585"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"48585":{"idvazba":"168019","nad_uzel":"136630","pod_uzel":"48585","url":"","sablona":"4","nazev":"Menova Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"15.07.2019 18:35:00","platne_do":null,"iduzel":"48585","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136631":{"idvazba":"168061","nad_uzel":"116995","pod_uzel":"136631","url":"\/research\/perlikova","sablona":"1","nazev":"Perl\u00edkov\u00e1 research group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova}","poradi":"10","skupina_www":"everyone","platne_od":"12.05.2026 22:04:00","platne_do":null,"iduzel":"136631","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:26:\"Perl\u00edkov\u00e1 research group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1264:\"<h1 style=\"text-align: center;\"><img src=\"\/files\/uzel\/0136631\/0009~~K0gtysnMzi9L1MvJT8_XLc5NzMkBAA.jpg\" class=\"img_fancy_no\" alt=\" \u25f3 perlikova.logo-small (jpg) \u2192 (\u0161\u00ed\u0159ka 215px)\" width=\"215\" height=\"168\"><\/h1>\r\n<h1 style=\"text-align: center;\">Medicinal chemistry of natural compound inspired scaffolds<\/h1>\r\n<p style=\"text-align: center;\">The research group led by Mgr.<em> et<\/em> Mgr. <strong>Pavla Perl\u00edkov\u00e1<\/strong>, Ph.D.<\/p>\r\n<p style=\"text-align: justify;\">Our research is focused on development of migrastatics using natural product-inspired scaffolds. We also work on development of antiparasitic compounds, namely with activity against trypanosomatids. In our projects, we are combining synthesis of complex molecules and medicinal chemistry.<\/p>\r\n<p>More details about the projects can be found in the&nbsp;<a href=\"perlikova-en\/research\" rel=\"follow\">Research<\/a>&nbsp;section.<\/p>\r\n<p><img src=\"\/files\/uzel\/0136631\/0006~~C09NMjIwMgEA.png\" alt=\" \u25f3 Web2024 (png) \u2192 (origin\u00e1l)\" width=\"620\" height=\"144\"><\/p>\r\n<p><\/p>\r\n<p><img src=\"\/files\/uzel\/0136631\/\/0010~~cy_KLy2I98svS81NSi2KNzIwMo03BAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Group_November_2025_1 (jpg) \u2192 (origin\u00e1l)\" width=\"620\" height=\"413\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["57799","136632","136633","57800","68595","136634"],"poduzly_count":6,"poduzly_count_aut":4,"poduzly":{"poduzly_count_aut_sum":1,"57799":{"idvazba":"168031","nad_uzel":"136634","pod_uzel":"57799","url":"","sablona":"4","nazev":"Dr. Perl\u00edkov\u00e1 group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"29.01.2024 22:57:00","platne_do":null,"iduzel":"57799","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136632":{"idvazba":"168022","nad_uzel":"136631","pod_uzel":"136632","url":"\/research\/perlikova\/Publications_clone_59553","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova\/Publications_clone_59553}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:35:23.209304","platne_do":null,"iduzel":"136632","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:5886:\"<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span style=\"font-size: 16.0pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: red; mso-fareast-language: CS;\">Publications<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoListParagraph\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><span>Saura, A.; Blahout, V.; Alpizar-Sosa, E. A.; Wen, H.; Reddy, A.; Prokopchuk, G.; Luke\u0161, J.; Kub\u00e1tov\u00e1, T.; Dehaen, W.; Rimpelov\u00e1, S.; Kostygov, A. Y.; Perl\u00edkov\u00e1, P.; Yurchenko, P.: Callunene, mitophagy, and flagellum removal in trypanosomatids.&nbsp;<\/span><i>Int. J. Parasitol.<\/i><span>&nbsp;<\/span><b>2026<\/b><span>,&nbsp;<\/span><i>56<\/i><span>, 104757. <a href=\"https:\/\/doi.org\/10.1016\/j.ijpara.2025.12.002\">DOI: 10.1016\/j.ijpara.2025.12.002<\/a><\/span><br><br>Javorsk\u00e1, \u017d.; Volfov\u00e1, T.; Faivre, J.; Dehaen, W.; Rimpelov\u00e1, S.; Lab\u00edkov\u00e1, M.; R\u00f6sel, D.; Br\u00e1bek, J.; Perl\u00edkov\u00e1, P.: Design and Synthesis of Actin-Targeting 10-Phenoxy Cytochalasan Analogues: Balancing Cytotoxicity and Migrastatic Activity. <em>ACS Med. Chem. Lett. <\/em><strong>2026<\/strong>, <em>17<\/em>, 409\u2013415. <a href=\"https:\/\/doi.org\/10.1021\/acsmedchemlett.5c00629\"><span style=\"text-decoration: underline;\">DOI: 10.1021\/acsmedchemlett.5c00629<\/span><\/a><br><br>Bro\u017e, A.; Volfov\u00e1, T.; Javorsk\u00e1, \u017d.; R\u00f6sel, D.; Br\u00e1bek, J. Perl\u00edkov\u00e1, P.: The potential of cytochalasins and other cytochalasans as drugs targeting cancer cell invasiveness and metastasis. <em>Eur. J. Med. Chem.<\/em> <strong>2026<\/strong>, <em>304<\/em>, 118502. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.ejmech.2025.118502\"><span style=\"text-decoration: underline;\">10.1016\/j.ejmech.2025.118502&nbsp;<\/span><\/a><br><br>Ferenczei, J.; Blahout, V.; Dvo\u0159\u00e1kov\u00e1, H.; Brancale, A.; Cu\u0159\u00ednov\u00e1, P.; Lab\u00edkov\u00e1, M.; Kohout, M.; Setni\u010dka, V.; Perl\u00edkov\u00e1, P.: Stereoanalysis of the antiparasitic natural product callunene and its synthetic intermediates. <em>J. Nat. Prod.<\/em> <strong>2025<\/strong>, <em>88<\/em>, 723\u2013731. <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jnatprod.4c01424\"><span style=\"text-decoration: underline;\">DOI: 10.1021\/acs.jnatprod.4c01424<\/span><\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoListParagraph\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">Javorsk\u00e1, \u017d.; Rimpelov\u00e1, S.; Lab\u00edkov\u00e1, M.; Perl\u00edkov\u00e1, P.: Synthesis of cytochalasan analogues with aryl substituents at position 10.<span>&nbsp;<\/span><i>Org. Biomol. Chem.<\/i><span>&nbsp;<\/span><b>2024<\/b>,<span>&nbsp;<\/span><i>22<\/i>, 4536-4549. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ob\/d4ob00634h\"><span style=\"text-decoration: underline;\">DOI: 10.1039\/d4ob00634h<\/span><\/a><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoListParagraph\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">Form\u00e1nek, B.; Dupommier, D.; Volfov\u00e1, T.; Rimpelov\u00e1, S.; \u0160karkov\u00e1, A.; Hercikov\u00e1, J.; R\u00f6sel, D.; Br\u00e1bek, J.; Perl\u00edkov\u00e1, P.: Synthesis and migrastatic activity of cytochalasin analogues lacking a macrocyclic moiety.&nbsp;<i style=\"mso-bidi-font-style: normal;\">RSC Med. Chem.<\/i> <b style=\"mso-bidi-font-weight: normal;\">2024<\/b>, <i style=\"mso-bidi-font-style: normal;\">15<\/i>, 322-343. DOI: <\/span><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/md\/d3md00535f\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; mso-fareast-language: CS;\">10.1039\/D3MD00535F<\/span><\/a><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">You can find older publications <\/span><a href=\"https:\/\/scholar.google.com\/citations?hl=cs&amp;user=YFaSAEwAAAAJ&amp;view_op=list_works\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; mso-fareast-language: CS;\">HERE<\/span><\/a><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">. <\/span><span lang=\"EN-US\" style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\"><o:p><\/o:p><\/span><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["57799","57800"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"57799":{"idvazba":"168031","nad_uzel":"136634","pod_uzel":"57799","url":"","sablona":"4","nazev":"Dr. Perl\u00edkov\u00e1 group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"29.01.2024 22:57:00","platne_do":null,"iduzel":"57799","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"57800":{"idvazba":"168028","nad_uzel":"136631","pod_uzel":"57800","url":"","sablona":"4","nazev":"Contact info","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"31.01.2023 19:32:00","platne_do":null,"iduzel":"57800","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136633":{"idvazba":"168025","nad_uzel":"136631","pod_uzel":"136633","url":"\/research\/perlikova\/open_clone_86380","sablona":"1","nazev":"Open positions","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova\/open_clone_86380}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:35:23.218846","platne_do":null,"iduzel":"136633","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:14:\"Open positions\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:904:\"<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 16.0pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: red; mso-ansi-language: EN-US; mso-fareast-language: CS;\">Open positions<o:p><\/o:p><\/span><\/p>\r\n<p>In the academic year 2026\/2027, one PhD topic will be available for a prospective student. If interested, please contact Pavla Perl\u00edkov\u00e1 by e-mail (<a href=\"mailto:perlikop@vscht.cz\">perlikop@vscht.cz<\/a>).<\/p>\r\n<p><span>You can find more information&nbsp;<\/span><a href=\"\/files\/uzel\/0074729\/0001~~88yrSi06vLBEISDDRdfVT9fIwMgMAA.pdf\"><u>here<\/u><\/a><\/p>\r\n<p>Students interested in carrying out their Bachelor\u2019s or Master\u2019s thesis in our group are welcome. Do not hesitate to get in touch.<br><br><br><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["57799","57800"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"57799":{"idvazba":"168031","nad_uzel":"136634","pod_uzel":"57799","url":"","sablona":"4","nazev":"Dr. Perl\u00edkov\u00e1 group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"29.01.2024 22:57:00","platne_do":null,"iduzel":"57799","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"57800":{"idvazba":"168028","nad_uzel":"136631","pod_uzel":"57800","url":"","sablona":"4","nazev":"Contact info","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"31.01.2023 19:32:00","platne_do":null,"iduzel":"57800","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"57800":{"idvazba":"168028","nad_uzel":"136631","pod_uzel":"57800","url":"","sablona":"4","nazev":"Contact info","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"31.01.2023 19:32:00","platne_do":null,"iduzel":"57800","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"68595":{"idvazba":"168029","nad_uzel":"136631","pod_uzel":"68595","url":"\/research\/perlikova\/research","sablona":"1","nazev":"Research topics of the group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova\/research}","poradi":"4","skupina_www":"everyone","platne_od":"04.01.2024 16:57:00","platne_do":null,"iduzel":"68595","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:28:\"Research topics of the group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:6521:\"<h1>Research topics of the group<\/h1>\r\n<h2>Migrastatics<\/h2>\r\n<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\">Metastasis accounts for more than 90% of cancer-related deaths. Despite recent advances in cancer therapies, the majority of patients with advanced-stage solid tumors die as a result of metastatic disease. Migrastatics represent a new concept of drugs with a great potential to improve the outcome of the current cancer treatment strategies by inhibiting metastatic behavior of cancer cells.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\">Our goal is to use rational design to synthesize new natural compound analogs with antimetastatic activity. We study structure-activity relationships. Our protein target is actin and actin polymerization regulators, such as the Arp2\/3 complex. Antimetastatic activity screening of the new compounds is performed in collaboration with Prof. Jan Br\u00e1bek group at BIOCEV (Vestec, Czechia).<o:p><\/o:p><\/span><\/p>\r\n<p><\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0068595\/0001~~C09NcvUzMjAy9s1ML0osLkksycxOBAA.png\" class=\"img_fancy_no\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 WebEN2023Migrastatika (png) \u2192 (origin\u00e1l)\" width=\"289\" height=\"177\"><\/p>\r\n<h3>Projects:<\/h3>\r\n<p>2023-2027: &nbsp;&nbsp;&nbsp;&nbsp; Development of actin polymerization inhibitors as potential migrastatics (GA\u010cR)<\/p>\r\n<p>2021-2022: &nbsp;&nbsp;&nbsp;&nbsp; Development of actin-targeting compounds with anti-metastatic effect (Dagmar Proch\u00e1zkov\u00e1 Fund)<\/p>\r\n<h2 style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #c45911; mso-themecolor: accent2; mso-themeshade: 191; mso-ansi-language: EN-US; mso-fareast-language: CS;\"><span class=\"modra0\"><br>Transcription factor inhibitors<\/span><\/span><\/span><\/h2>\r\n<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\">The regulation of cell signaling is one of the most common mechanisms of action for drugs. It is possible to affect cell receptors as well as signal transduction within the cell. Gene expression can also be affected indirectly. However, direct regulation of protein expression by targeting transcription factors is challenging. So far, only a small fraction of them, the so-called nuclear receptors, have been exploited because most transcription factors do not contain binding sites for small molecules.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\">In our group, we are working on the rational design of inhibitors of other transcription factors involved in metabolic disorders such as diabetes, obesity and infertility. In this project we collaborate within the VS\u010cHT with the groups of prof. Andrea Brancale and Prof. Daniel Svozil.<o:p><\/o:p><\/span><\/p>\r\n<h3 style=\"margin-bottom: 5.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\"><span class=\"modra0\">Projects: <\/span><o:p><\/o:p><\/span><\/h3>\r\n<p style=\"margin-bottom: .0001pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\">2024-2028: <span style=\"mso-tab-count: 1;\">&nbsp;&nbsp;&nbsp;&nbsp; <\/span>NETPHARM: New technologies for translational research in pharmaceutical sciences (OP JAK)<o:p><\/o:p><\/span><\/p>\r\n<p>&nbsp;<\/p>\r\n<h2>Antiparasitic compounds<\/h2>\r\n<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span lang=\"EN-US\" style=\"font-size: 11.5pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-ansi-language: EN-US; mso-fareast-language: CS;\"><br>Trypanosomatids are causative agents of several diseases transmitted by insects: Chagas disease (<i style=\"mso-bidi-font-style: normal;\">Trypanosoma cruzi<\/i>), human african trypanosomiasis known as \u201esleeping sickness\u201c (<i style=\"mso-bidi-font-style: normal;\">Trypanosoma b. gambiense<\/i>, <i style=\"mso-bidi-font-style: normal;\">Trypanosoma b. rhodesiense<\/i>) and leishmaniasis (<i style=\"mso-bidi-font-style: normal;\">Leishmania sp.<\/i>). The current treatment of these diseases is complicated. Therefore, we study natural compounds, elucidate their mechanism of action and synthesize their analogs for further development as potential drugs. New compounds are developed in collaboration with the group of Prof. Vyacheslav Yurchenko (University of Ostrava).<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: center;\"><img src=\"\/images\/450!0\/uzel\/0068595\/0003~~c8wryQwAAA.png\" alt=\" \u25f3 AntiP (png) \u2192 (\u0161\u00ed\u0159ka 450px)\" width=\"293\" height=\"177\"><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["57799","57800"],"poduzly_count":2,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"57799":{"idvazba":"168031","nad_uzel":"136634","pod_uzel":"57799","url":"","sablona":"4","nazev":"Dr. Perl\u00edkov\u00e1 group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"29.01.2024 22:57:00","platne_do":null,"iduzel":"57799","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"57800":{"idvazba":"168028","nad_uzel":"136631","pod_uzel":"57800","url":"","sablona":"4","nazev":"Contact info","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"31.01.2023 19:32:00","platne_do":null,"iduzel":"57800","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136634":{"idvazba":"168030","nad_uzel":"136631","pod_uzel":"136634","url":"\/research\/perlikova\/people_clone_21544","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova\/people_clone_21544}","poradi":"5","skupina_www":"everyone","platne_od":"04.09.2026 12:28:00","platne_do":null,"iduzel":"136634","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1134:\"<h1>People in research group<\/h1>\r\n<h3>Group leader:<\/h3>\r\n<ul>\r\n<li><a href=\"\/\/uoch.vscht.cz\/research-groups\/perlikova-en\/people\/Perlikova_CV\" target=\"_blank\" rel=\"noopener\">Pavla Perl\u00edkov\u00e1<\/a><\/li>\r\n<\/ul>\r\n<h3>Postdoc researcher:<\/h3>\r\n<ul>\r\n<li>Vahid Barati<\/li>\r\n<\/ul>\r\n<h3>PhD students:<\/h3>\r\n<ul>\r\n<li>Michal Trojan<\/li>\r\n<li>Katarzyna Kwieci\u0144ska<\/li>\r\n<li>Isabela Whelanov\u00e1<\/li>\r\n<li>Antonietta de Falco<\/li>\r\n<\/ul>\r\n<h3>Students:<\/h3>\r\n<ul>\r\n<li>Artem Lobanov<\/li>\r\n<li>Ad\u00e9la Nemejtov\u00e1<\/li>\r\n<li>Aneta Pokorn\u00e1<\/li>\r\n<li>Karol\u00edna Sou\u010dkov\u00e1<\/li>\r\n<\/ul>\r\n<h3>Laboratory staff:<\/h3>\r\n<p>Kv\u011bta B\u00e1rtov\u00e1<\/p>\r\n<h3>Alumni:<\/h3>\r\n<p>Bed\u0159ich Form\u00e1nek<\/p>\r\n<p>Vil\u00e9m Blahout<\/p>\r\n<p>Tereza Kub\u00e1tov\u00e1<\/p>\r\n<p>Dorian Dupommier<\/p>\r\n<p>Daniel Kozov\u00fd<\/p>\r\n<p>Ji\u0159\u00ed Ferenczei<\/p>\r\n<p>\u017daneta Javorsk\u00e1<\/p>\r\n<p>Mat\u011bj \u0158\u00edha<\/p>\r\n<p>Veronika \u0160vecov\u00e1<\/p>\r\n<p>Nat\u00e1lie Vl\u010dkov\u00e1<\/p>\r\n<p>&nbsp;<img src=\"\/images\/0!0\/uzel\/0057798\/0004~~cy_KLy2I98svS81NSi2KNzIwMo03BAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 Group_November_2025_1 (jpg) \u2192 (origin\u00e1l)\" width=\"620\" height=\"413\"><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["57799","136635","57800"],"poduzly_count":3,"poduzly_count_aut":1,"poduzly":{"poduzly_count_aut_sum":0,"57799":{"idvazba":"168031","nad_uzel":"136634","pod_uzel":"57799","url":"","sablona":"4","nazev":"Dr. Perl\u00edkov\u00e1 group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"29.01.2024 22:57:00","platne_do":null,"iduzel":"57799","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136635":{"idvazba":"168032","nad_uzel":"136634","pod_uzel":"136635","url":"\/research\/perlikova\/people_clone_21544\/Perlikova_CV_clone_27596","sablona":"1","nazev":"Mgr. et Mgr. Pavla Perl\u00edkov\u00e1, Ph.D.","_url_prefix":"{\/\/uoch.vscht.cz\/research\/perlikova\/people_clone_21544\/Perlikova_CV_clone_27596}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:35:23.324286","platne_do":null,"iduzel":"136635","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:37:\"Mgr. et Mgr. Pavla Perl\u00edkov\u00e1, Ph.D.\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:9870:\"<p style=\"margin-bottom: 15.0pt; text-align: justify; line-height: normal; background: white;\" class=\"MsoNormal\"><span style=\"font-size: 16.0pt; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: red; mso-fareast-language: CS;\">Mgr. <i style=\"mso-bidi-font-style: normal;\">et<\/i> Mgr. Pavla Perl\u00edkov\u00e1, Ph.D.<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">e-mail: <\/span><a href=\"mailto:perlikop@vscht.cz\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; mso-fareast-language: CS;\">perlikop@vscht.cz<\/span><\/a><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">phone: +420 220442039<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">Born 10. 3. 1984 in Ostrava (Czech Republic).<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><strong>Scientific CV:<\/strong><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2003-2006 undergraduate study, Charles University in Prague - Faculty of Science, Bc. S. degree - specialization organic chemistry (supervisor Dr. Jan \u0160arek)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2004-2007 undergraduate study, Charles University in Prague - Faculty of Science, Bc. S. degree - specialization molecular biology and biochemistry (supervisor Associate Prof. Mari\u00e1n Hajd\u00fach)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2006-2008 undergraduate study, Charles University in Prague - Faculty of Science, M. S. degree - specialization organic chemistry (supervisor RNDr. Jan \u0160arek, Ph.D.)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2007-2009 undergraduate study, Charles University in Prague - Faculty of Science, M. S. degree - specialization cell biology (supervisor Associate Prof. Mari\u00e1n Hajd\u00fach)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2008-2012 PhD study, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic (supervisor Dr. M. Hocek)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2012-2013 postdoctoral position, University of Southern Denmark (supervisor prof. Jesper Wengel)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2013-2020 postdoctoral position, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic (supervisor Dr. M. Hocek)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">since 2021 assistant professor, University of Chemistry and Technology Prague<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><strong>Awards:<\/strong><o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2008 Zentiva award for the best diploma thesis<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2011 Best oral presentation, XV Symposium on Chemistry of Nucleic Acid Components, \u010cesk\u00fd Krumlov<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2012 Prix Sanofi Pharmacie (3rd position)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2017 Otto Wichterle Award<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">2019 Alfred Bader Prize for Bioorganic and Bioinorganic Chemistry (CAB II 2019)<o:p><\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p>&nbsp;<\/o:p><\/span><\/p>\r\n<p style=\"text-align: justify;\" class=\"MsoNormal\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\">Publications <\/span><a href=\"https:\/\/scholar.google.com\/citations?hl=cs&amp;user=YFaSAEwAAAAJ&amp;view_op=list_works\"><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; mso-fareast-language: CS;\">HERE<\/span><\/a><span style=\"font-size: 11.5pt; line-height: 107%; font-family: 'source_sans_proregular',serif; mso-fareast-font-family: 'Times New Roman'; mso-bidi-font-family: 'Times New Roman'; color: #333333; mso-fareast-language: CS;\"><o:p><\/o:p><\/span><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"57800":{"idvazba":"168028","nad_uzel":"136631","pod_uzel":"57800","url":"","sablona":"4","nazev":"Contact info","_url_prefix":null,"poradi":"3","skupina_www":"everyone","platne_od":"31.01.2023 19:32:00","platne_do":null,"iduzel":"57800","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"136636":{"idvazba":"168062","nad_uzel":"116995","pod_uzel":"136636","url":"\/research\/svoboda","sablona":"1","nazev":"Kohout","_url_prefix":"{\/\/uoch.vscht.cz\/research\/svoboda}","poradi":"11","skupina_www":"everyone","platne_od":"12.05.2026 21:35:38.266908","platne_do":null,"iduzel":"136636","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"Kohout\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:46:\"<p>The page has not been synthesized yet..<\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38654","136637","136638","136639"],"poduzly_count":4,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":0,"38654":{"idvazba":"168041","nad_uzel":"136639","pod_uzel":"38654","url":"","sablona":"4","nazev":"Svoboda's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.03.2017 16:57:00","platne_do":null,"iduzel":"38654","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136637":{"idvazba":"168036","nad_uzel":"136636","pod_uzel":"136637","url":"\/research\/svoboda\/people_clone_60011","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/svoboda\/people_clone_60011}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:35:38.297255","platne_do":null,"iduzel":"136637","obsah":"a:7:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:2472:\"<h3><strong>Staff:<\/strong><\/h3>\r\n<ul>\r\n<li>Prof. Ji\u0159\u00ed Svoboda<\/li>\r\n<li><a href=\"\/vedecke-skupiny\/svoboda\/lide\/kohout\" rel=\"follow\">Assoc. Prof. Michal Kohout<\/a><\/li>\r\n<li>Dr. V\u00e1clav Kozm\u00edk, CSc.<\/li>\r\n<li>MSc. Mark\u00e9ta Slabochov\u00e1<br \/><br \/><br \/><\/li>\r\n<\/ul>\r\n<h3 class=\"podnadpis\"><strong>PhD Students:<\/strong><\/h3>\r\n<ul>\r\n<li class=\"podnadpis\">MSc. Kvetoslava Bajz\u00edkov\u00e1<\/li>\r\n<li>MSc. Anna Poryvai<\/li>\r\n<li>MSc. Jana Hercikov\u00e1<\/li>\r\n<li>MSc. Michal \u0160mahel<\/li>\r\n<\/ul>\r\n<h5>\u00a0<\/h5>\r\n<h3 class=\"podnadpis\"><strong>Undergraduate Students:<\/strong><\/h3>\r\n<p class=\"podnadpis\"><u>Master Study, 2nd year<\/u><\/p>\r\n<ul>\r\n<li>Bc. Tereza \u010cern\u00e1<\/li>\r\n<li>Bc. Nat\u00e1lie Kolderov\u00e1<\/li>\r\n<li>Bc. Martin Pa\u0161kan<\/li>\r\n<li>Bc. Karol\u00edna Zvolsk\u00e1<br \/><br \/><\/li>\r\n<\/ul>\r\n<p><u>Bachelor Study, 3rd year<\/u><\/p>\r\n<ul>\r\n<li>Jaroslav Cerman<\/li>\r\n<li>Diana J\u00e1gerov\u00e1<\/li>\r\n<li>\u017daneta Javorsk\u00e1<\/li>\r\n<li>Tereza Ludv\u00edkov\u00e1<\/li>\r\n<li>Eva Tetenkov\u00e1<\/li>\r\n<li>Adam V\u00edt<br \/><br \/><\/li>\r\n<\/ul>\r\n<p><u>Bachelor Study, 2nd year<\/u><\/p>\r\n<ul>\r\n<li>Jakub D\u00e1vid Malina<\/li>\r\n<li>Anna Rejzkov\u00e1<br \/><br \/><\/li>\r\n<\/ul>\r\n<p class=\"podnadpis\"><\/p>\r\n<h4 class=\"podnadpis\"><strong>Alumni:<\/strong><\/h4>\r\n<ul>\r\n<li>Ing. Miloslav Ni\u010d, Ph.D.<\/li>\r\n<li>Ing. Pavel Pihera, CSc.<\/li>\r\n<li>Ing. Miroslav Terinek, Ph.D.<\/li>\r\n<li>Ing. Marie Havelkov\u00e1<\/li>\r\n<li>Ing. Petr V\u00e1chal, Ph.D.<\/li>\r\n<li>Ing. Kate\u0159ina \u010cernovsk\u00e1, Ph.D.<\/li>\r\n<li>Ing. Kate\u0159ina Dudov\u00e1<\/li>\r\n<li>Ing. Petr Vodi\u010dka, Ph.D.<\/li>\r\n<li>Ing. Lech Mr\u00f3zek, Ph.D.<\/li>\r\n<li>Ing. Bed\u0159ich Ko\u0161ata, Ph.D.<\/li>\r\n<li>Ing. Marie M\u00e9zlov\u00e1, Ph.D.<\/li>\r\n<li>Ing. Michal Rej\u0148\u00e1k<\/li>\r\n<li>Ing. Milan Kurf\u00fcrst, Ph.D.<\/li>\r\n<li>Ing. Ale\u0161 Machara, Ph.D.<\/li>\r\n<li>Ing. Martin Kucha\u0159, Ph.D.<\/li>\r\n<li>Ing. Michal Kohout, Ph.D.<\/li>\r\n<li>Ing. Anna Kov\u00e1\u0159ov\u00e1, Ph.D.<\/li>\r\n<li>Ing. Petr Hadrava<\/li>\r\n<li>Ing. Adam Henke, Ph.D.<\/li>\r\n<li>Ing. Ji\u0159\u00ed \u017durek, Ph.D.<\/li>\r\n<li>Ing. Petr Pol\u00e1\u0161ek<\/li>\r\n<li>Ing. Petr \u0160pa\u010dek<\/li>\r\n<li>Ing. Arno\u0161t Seidler<\/li>\r\n<li>Ing. Lucie \u0158ehov\u00e1<\/li>\r\n<li>Ing. Svatopluk Sv\u011btl\u00edk<\/li>\r\n<li>Ing. Ji\u0159\u00ed Vesel\u00fd<\/li>\r\n<li>Ing. Michal Pozn\u00edk<\/li>\r\n<li>Ing. Michal M\u00e1jek<\/li>\r\n<li>Ing. Ond\u0159ej P\u00ed\u0161a<\/li>\r\n<li>Ing. Eva Rodinov\u00e1<\/li>\r\n<li>Ing. Kvetoslava Bajz\u00edkov\u00e1<\/li>\r\n<li>Ing. Martin Hor\u010dic<\/li>\r\n<li>Ing. Ji\u0159\u00ed T\u016fma<\/li>\r\n<li>Ing. Anna Poryvai<\/li>\r\n<li>Ing. Lenka Pallov\u00e1<\/li>\r\n<li>Ing. Helena Skopalov\u00e1<\/li>\r\n<li>Ing. Tom\u00e1\u0161 Hod\u00edk<\/li>\r\n<li>Ing. Tereza Prausov\u00e1<\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38654"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38654":{"idvazba":"168041","nad_uzel":"136639","pod_uzel":"38654","url":"","sablona":"4","nazev":"Svoboda's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.03.2017 16:57:00","platne_do":null,"iduzel":"38654","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136638":{"idvazba":"168038","nad_uzel":"136636","pod_uzel":"136638","url":"\/research\/svoboda\/research_clone_71454","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/svoboda\/research_clone_71454}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:35:38.323361","platne_do":null,"iduzel":"136638","obsah":"a:6:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:46:\"<p>The page has not been synthesized yet..<\/p>\";}","class":"stranka","autonomni":"1","pod_uzly":["38654"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38654":{"idvazba":"168041","nad_uzel":"136639","pod_uzel":"38654","url":"","sablona":"4","nazev":"Svoboda's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.03.2017 16:57:00","platne_do":null,"iduzel":"38654","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136639":{"idvazba":"168040","nad_uzel":"136636","pod_uzel":"136639","url":"\/research\/svoboda\/publications_clone_76637","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/svoboda\/publications_clone_76637}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:35:38.376008","platne_do":null,"iduzel":"136639","obsah":"a:7:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:37688:\"<h3>2019<br \/><br \/><\/h3>\r\n<ul>\r\n<li>Jing, H.; Xu, M.; Xiang, Y.; Wang, E.; Liu, D.; Poryvai, A.; Kohout, M.; \u00c9ber, N.; Buka, A.:<br \/>Light tunable gratings based on flexoelectric effect in photoresponsive bent-core nematics. <br \/><em>Adv. Opt. Mater.<\/em> <strong>2019<\/strong>, 1801790 DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1002\/adom.201801790\" class=\"epub-doi\" aria-label=\"Digital Object Identifier\">10.1002\/adom.201801790<\/a><br \/><br \/><\/li>\r\n<li>Pokluda, A.; Kohout, M.; Chudoba, J.; Krupi\u010dka, M.; Cibulka, R.: <br \/>Nitrosobenzene: Reagent for the Mitsunobu esterification reaction.<br \/><em>ACS Omega<\/em> <strong>2019<\/strong>, <em>4<\/em>, 5012-5018 DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acsomega.8b03551\" title=\"DOI URL\">10.1021\/acsomega.8b03551<\/a><br \/><br \/><\/li>\r\n<li>Sp\u00e1lovsk\u00e1, D.; Ma\u0159\u00edkov\u00e1, T.; Kohout, M.; Kr\u00e1l\u00edk, F.; Kucha\u0159, M.; Setni\u010dka, V.: <br \/>Methylone and pentylone: Structural analysis of new psychoactive substances. <br \/><em>Forensic Toxicol.<\/em> <strong>2019<\/strong>, <em>37<\/em>, 366-377 DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1007\/s11419-019-00468-z\" rel=\"follow\">10.1007\/s11419-019-00468-z<\/a><br \/><br \/><\/li>\r\n<li>Poryvai, A.; Bubnov, A.; Pociecha, D.; Svoboda, J.; Kohout, M.: <br \/>The effect of the length of terminal n-alkyl carboxylate chain of self-assembling and photosensitive properties of chiral lactic acid derivatives. <br \/><em>J. Mol. Liq.<\/em> <strong>2019<\/strong>, <em>275<\/em>, 829-838 DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.molliq.2018.11.058\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.molliq.2018.11.058<\/a><br \/><br \/><\/li>\r\n<li>Geibel, C.; Dittrich, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; L\u00e4mmerhofer, M.: <br \/>Evaluation of superficially porous particle based zwitterionic chiral ion exchangers against fully porous particle benchmarks for enantioselective ultra-high performance liquid chromatography. <br \/><em>J. Chromatogr. A<\/em> <strong>2019<\/strong>, <em>1603<\/em>, 130-140 DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.chroma.2019.06.026\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.chroma.2019.06.026<\/a><br \/><br \/><\/li>\r\n<li>Poryvai, A.; Vojtylov\u00e1-Jurkovi\u010dov\u00e1, T.; \u0160mahel, M.; Kolderov\u00e1, N.; Tom\u00e1\u0161kov\u00e1, P.; S\u00fdkora, D.; Kohout, M.: <br \/>Determination of optical purity of lactic acid-based chiral liquid crystals and corresponding building blocks by chiral high-performance liquid chromatography and supercritical fluid chromatography. <br \/><em>Molecules<\/em> <strong>2019<\/strong>, <em>24<\/em>, 1099 DOI:\u00a0<a href=\"https:\/\/dx.doi.org\/10.3390%2Fmolecules24061099\" target=\"pmc_ext\">10.3390\/molecules24061099<\/a><br \/><br \/><\/li>\r\n<li>Tlust\u00fd, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhot\u00e1k, P.: <br \/>Synthesis of upper rim-double-bridged calix[4]arenes bearing seven membered rings and related compounds. <br \/><em>RSC Adv.<\/em> <strong>2019<\/strong>, <em>9<\/em>, 22017-22030. DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C9RA05075B\" rel=\"follow\">10.1039\/C9RA05075B<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<p><\/p>\r\n<h3>2018<\/h3>\r\n<ul>\r\n<li><span class=\"cerna0\"><span class=\"\"><span style=\"font-size: 12.0pt; color: black;\"><span class=\"cerna0\">Jur\u00e1sek, B.; Kr\u00e1l\u00edk, F.; Rimpelov\u00e1 S.; \u010cejka, J.; Setni\u010dka, V.; Ruml, T.; Kucha\u0159, M.; <span class=\"\">Kohout, M.<\/span>:<\/span><br \/><span class=\"cerna0\">Synthesis, Absolute Configuration and <em>in vitro<\/em> Cytotoxicity of Deschloroketamine Enantiomers: Rediscovered and Abused Dissociative Anaesthetic <br \/><em>New. J. Chem.<\/em> <strong>2018<\/strong>, <em>42<\/em>, 19360-19368 DOI: <\/span><a href=\"http:\/\/dx..doi.org\/10.1039\/c8nj03107j\" rel=\"follow\"><\/a><a href=\"http:\/\/dx..doi.org\/10.1039\/c8nj03107j\" rel=\"follow\">10.1039\/c8nj03107j<\/a><\/span><br \/>COVER<\/span><\/span><br \/><img src=\"\/images\/215!0\/uzel\/0038647\/0001~~S84vSy1S8M7PyC8tUcgpBAA.png\" style=\"border-style: solid; border-width: 1px;\" alt=\"New. J. Chem. 2018, 42, 19360-19368 DOI: 10.1039\/c8nj03107j\" width=\"215\" height=\"281\" \/><br \/><br \/><\/li>\r\n<li>Schmitt, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; L\u00e4mmerhofer, M.: <br \/>Comparison of small size fully porous particles and superficially porous particles of chiral anion-exchange type stationary phases in ultra-high performance liquid chromatography: effect of particle and pore size on chromatographic efficiency and kinetic performance<br \/><em>J. Chromatogr. A<\/em> <strong>2018<\/strong>, <em>1569<\/em>, 149-159 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.chroma.2018.07.056\" rel=\"follow\">10.1016\/j.chroma.2018.07.056<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>Sp\u00e1lovsk\u00e1, D.; Kralik, F.; Kohout, M.; Jurasek, B.; Habartov\u00e1, L.; Kuchar, M.; Setnicka, V.:\u00a0<br \/>Structure determination of butylone as a new psychoactive substance using chiroptical and vibrational spectroscopies\u00a0<br \/><em>Chirality<\/em> <strong>2018<\/strong>, <em>30<\/em>, 548-559 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/chir.22825\" rel=\"follow\">10.1002\/chir.22825<\/a><br \/><br \/><\/li>\r\n<li>Wolrab, D.; Kohout, M.: <br \/>Multimod\u00e1ln\u00ed stacion\u00e1rn\u00ed f\u00e1ze pro kapalinovou chromatografii, zp\u016fsob jejich p\u0159\u00edpravy a jejich pou\u017eit\u00ed. <br \/>N\u00e1rodn\u00ed patent \u010d. 307339, \u010d\u00edslo p\u0159ihl\u00e1\u0161ky 2017-193, datum ud\u011blen\u00ed 2.5.2018, datum zve\u0159ejn\u011bn\u00ed 13.6.2018.<br \/><br \/><\/li>\r\n<li>Kohout, M.; Wernisch, S.; Tuma, J.; Hettegger, H.; Picha, J.; Lindner W.:\u00a0<br \/>Effect of different immobilization strategies on chiral recognition properties of Cinchona-based anion exchangers\u00a0<br \/><em>J. Sep. Sci.<\/em> <strong>2018<\/strong>, <em>41<\/em>, 1355-1364 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701213\" rel=\"follow\">10.1002\/jssc.201701213<\/a><br \/><br \/><\/li>\r\n<li>Bajtai, A.; Fekete, B.; Palk\u00f3, M.; F\u00fcl\u00f6p, F.; Lindner, W.; Kohout, M.; Ilisz, I.; P\u00e9ter, A.:\u00a0<br \/>Comparative study on the liquid chromatographic enantioseparation of cyclic \u03b2-amino acids and the related cyclic \u03b2-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases\u00a0<br \/><em>J. Sep. Sci.<\/em> <strong>2018<\/strong>, <em>41<\/em>, 1216-1223 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701190\" rel=\"follow\">10.1002\/jssc.201701190<\/a><br \/><br \/><\/li>\r\n<li>Sardella, R.; Macchiarulo, A.; Urbinati, F.; Ianni, F.; Carotti, A.; Kohout, M.; Lindner, W.; P\u00e9ter, A.; Ilisz, I.:\u00a0<br \/>Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers\u00a0<br \/><em>J. Sep. Sci.<\/em> <strong>2018<\/strong>, <em>41<\/em>, 1199-1207 DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jssc.201701068\" rel=\"follow\">10.1002\/jssc.201701068<\/a><br \/><br \/><\/li>\r\n<li>Tuma, J.; Kohout, M.:\u00a0<br \/>Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation\u00a0<br \/><em>RSC Adv.<\/em> <strong>2018<\/strong>, <em>8<\/em>, 1174-1181 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/c7ra12658a\" rel=\"follow\">10.1039\/c7ra12658a<\/a><br \/><br \/><\/li>\r\n<li>Kozmik, V.; Rodinov\u00e1, E.; Prausov\u00e1, T.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: <br \/>Mesogens with central naphthalene core substituted at various positions\u00a0<br \/>Liq. Cryst. <strong>2018<\/strong>, 45, 744-756 DOI: <a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2017.1380238\" rel=\"follow\">10.1080\/02678292.2017.1380238<\/a><br \/><br \/><\/li>\r\n<li><em>\u00a0<\/em>Bajz\u00edkov\u00e1, K.; Vesely, J.; Kozmik, V.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: <br \/>Thiophene\u00a0central core for the design of bent-shaped liquid crystals\u00a0<br \/><em>J. Mol. Liq.<\/em> <strong>2018<\/strong>, <em>267<\/em>, 496-503\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.molliq.2018.02.009\" rel=\"follow\">10.1016\/j.molliq.2018.02.009<\/a><br \/><br \/><\/li>\r\n<li>Horcic, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.; Gorecka, E.: <br \/>Bent-core dimers with top-to-bottom linkage between central units\u00a0<br \/>RSC Adv. <strong>2018<\/strong>, <strong><em>8<\/em><\/strong>, 22974-22985 DOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/c8ra04108c\" rel=\"follow\">10.1039\/c8ra04108c<\/a><br \/><br \/><\/li>\r\n<li><span class=\"modra0\"><span class=\"cerna0\">Marz, M.; Kohout, M.; Nevesely, T.; <span class=\"\">Chudoba, J.; Prukala, D.; Nizinski, S.; Sikorski, M.; Burdzinski, G.; <\/span>Cibulka, R.:<\/span><br \/><span class=\"cerna0\">Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control<\/span><br \/><\/span><em>Org. Biomol. Chem.<\/em>\u00a0<strong>2018<\/strong>, <em>16<\/em>, 6809-6817 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C8OB01822G\" rel=\"follow\">10.1039\/C8OB01822G<\/a><br \/><br \/><\/li>\r\n<\/ul>\r\n<h3>2017<\/h3>\r\n<ul>\r\n<li>Maixner, J.; Jur\u00e1sek, B.; Kohout, M.; Kuchar, M.; Kacer, P.:<br \/>X-ray powder diffraction data for (S)-Deschloroketamine hydrochloride, C<sub>13<\/sub>H<sub>18<\/sub>ClNO. <br \/><em>Powder Diffr.<\/em> <strong>2017<\/strong>, <em>32<\/em>, 193-195. DOI:<a href=\"http:\/\/dx.doi.org\/10.1017\/S0885715617000586\" rel=\"follow\">10.1017\/S0885715617000586<\/a><br \/><br \/><\/li>\r\n<li>Bajz\u00edkov\u00e1, K.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.; Gorecka E.: <br \/>Bent-core mesogens with an aromatic unit at the terminal position<br \/><em>New J. Chem.<\/em> <strong>2017<\/strong>, <em>41<\/em>,\u00a04672-4679 DOI: <a href=\"http:\/\/dx.doi.org\/10.1039\/C6NJ03908A\" rel=\"follow\"><span class=\"list__item-data\">10.1039\/C6NJ03908A<\/span><\/a><br \/><br \/><\/li>\r\n<li><span class=\"modra0\"><span class=\"cerna0\">\u017durek, J.; Svobodov\u00e1, E.<\/span><\/span>; \u0160turala, J.; Dvo\u0159\u00e1kov\u00e1, H.;<span class=\"cerna0\"> <span class=\"\">Svoboda, J.; Cibulka, R.<\/span>:<\/span><br \/>Chiral ethylene-bridged flavinium salts: The stereoselectivity of flavin-10a-hydroperoxide formation and the effect of substitution on the photochemical properties <br \/><em>Tetrahedron Asymmetry<\/em> <strong>2017<\/strong>, asap DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetasy.2017.10.029\" rel=\"follow\">10.1016\/j.tetasy.2017.10.029<\/a><br \/><br \/><\/li>\r\n<\/ul>\r\n<ul>\r\n<li>Dobrovolny, K.; Ulbrich, P.; Svecova, M.; Rimpelova, S.; <span class=\"cerna0\"><span class=\"\">Malincik, J.; <span class=\"hit\">Kohout, M.<\/span>; Svoboda, J.<\/span>; Bartunek, V.:\u00a0<\/span><br \/>Copper nanoparticles in glycerol-\u200bpolyvinyl alcohol matrix: In situ preparation, stabilization and antimicrobial activity<br \/><span class=\"biblioTitle\"><em>Journal of Alloys and Compounds<\/em> <strong>2017<\/strong>,<em> 697<\/em>, 147-155 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jallcom.2016.12.144\" rel=\"follow\">10.1016\/j.jallcom.2016.12.144<br \/><br \/><\/a><\/span><\/li>\r\n<li>Kolderova, N.; <span class=\"cerna0\"><span class=\"\">Nevesely, T.; Sturala, J.<\/span>; Kuchar, M.; <\/span><span class=\"cerna0\"><span class=\"\">Holakovsky, R.<\/span><span class=\"modra0\">; <\/span><\/span><span class=\"modra0\"><span class=\"hit\">Kohout, M.<\/span><\/span><span class=\"hit\">:<br \/><\/span>Enantioseparation of chiral sulfoxides on amylose-\u200bbased columns: comparison of normal phase liquid chromatography and supercritical fluid chromatography<br \/><em>Chromatographia<\/em> <strong>2017<\/strong>, <em>80<\/em>, 547-557 DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1007\/s10337-016-3234-6\" rel=\"follow\">10.1007\/s10337-016-3234-6<\/a><br \/><br \/><\/li>\r\n<li><span class=\"cerna0\"><span class=\"hit\"><span class=\"\">Kohout, M.<\/span><\/span>; Alaasar, M<\/span><span class=\"cerna0\"><span class=\"\">.; <span class=\"\">Poryvai, A.<\/span>; Novotna, V.; Poppe, S.; Tschierske, C.; <span class=\"cerna0\"><span class=\"\">Svoboda, J.<\/span>:<\/span><\/span>\u00a0<\/span><br \/>Photosensitive bent-\u200bcore liquid crystals based on methyl substituted 3-\u200bhydroxybenzoic acid<br \/><em>RSC Advances<\/em> <strong>2017<\/strong>, <em>7<\/em>, 35805-35813 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7RA05632J\" rel=\"follow\">10.1039\/C7RA05632J<\/a><br \/><br \/><\/li>\r\n<li>Wolrab, D.; Fruehauf, P.; Gerner, C.; <span class=\"hit\"><span class=\"modra0\"><span class=\"cerna0\">Kohout, M.<\/span><\/span>;<\/span>\u00a0Lindner, W.:\u00a0<br \/>Consequences of transition from liquid chromatography to supercritical fluid chromatography on the overall performance of a chiral zwitterionic ion-\u200bexchanger<br \/><em>Journal of Chromatography A<\/em> <strong>2017<\/strong>, <em>1517<\/em>, 165-175 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.chroma.2017.08.022\" rel=\"follow\">10.1016\/j.chroma.2017.08.022<\/a><br \/><br \/><\/li>\r\n<li><span class=\"modra0\"><span class=\"cerna0\">Pallova, L.;<\/span> <span class=\"\"><span class=\"hit\">Kozmik, V.<\/span><\/span><\/span><span class=\"cerna0\"><span class=\"\">; Kohout, M.; Svoboda, J.<\/span>;<\/span> Novotna, V.; Pociecha, D.:\u00a0<br \/>Bent-\u200bcore liquid crystals with a 2-\u200bsubstituted 3-\u200bhydroxybenzoic acid central core<br \/><em>Liquid Crystals<\/em> <strong>2017<\/strong>, <em>44<\/em>, 1306-1315 DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1276981\" rel=\"follow\">10.1080\/02678292.2016.1276981<br \/><br \/><\/a><\/li>\r\n<\/ul>\r\n<ul>\r\n<li><span class=\"cerna0\"><span class=\"\">Tlusty, M.; Slavik, P.; Kohout, M.; Eigner, V.; Lhotak, P.:<br \/>Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring<br \/><em>Org. Lett.<\/em>\u00a0<strong>2017<\/strong>, <em>19<\/em>, 2933-2936 DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b01170\">10.1021\/acs.orglett.7b01170<\/a><br \/><br \/><\/span><\/span><\/li>\r\n<li><span class=\"cerna0\"><span class=\"\">Miksatko, J.<\/span>; Eigner, V.;<span class=\"modra0\"> <span class=\"cerna0\">Kohout, M.; Lhotak, P.:<\/span><\/span><\/span><br \/>Regio-\/stereoselective Formation of Monosulfoxides from Thiacalix[4]arenes in All Possible Conformations<br \/><em><span class=\"cerna0\">Tetrahedron Letters<\/span><\/em> <strong>2017<\/strong><span class=\"cerna0\">, <em>58<\/em>, 1687\u20131691 DOI:<\/span><a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2017.03.043\" target=\"doilink\" id=\"ddDoi\" class=\"S_C_ddDoi\">10.1016\/j.tetlet.2017.03.043<br \/><br \/><\/a><\/li>\r\n<li><span class=\"\"><span class=\"cerna0\"><span style=\"color: #00add2;\"><span class=\"cerna0\">Hor\u010dic, M.; Kohout, M.; <span class=\"\">Svoboda, J.<\/span>; Novotna, V.; Pociecha, D.; Gorecka, E.:<br \/>Core-to-core Dimers Forming Switchable Mesophase<br \/><em>Chem. \u00a0Commun.<\/em>\u00a0<strong>2017<\/strong>, <span style=\"font-size: 15px;\"><em>53<\/em><\/span>, 2721-2724 DOI:<\/span><a href=\"http:\/\/dx.doi.org\/10.1039\/C6CC09983A\">10.1039\/C6CC09983A<\/a><br \/><br \/><\/span><\/span><\/span><\/li>\r\n<li><span class=\"\"><span class=\"cerna0\"><span class=\"cerna0\"><span class=\"cerna0\"><span style=\"color: #00add2;\"><span class=\"cerna0\">M\u00e4rz, M.; <\/span><\/span><\/span><span class=\"cerna0\"><span class=\"\"><span class=\"cerna0\"><span style=\"color: #00add2;\"><span class=\"cerna0\">Chudoba, J.;<\/span><\/span> <\/span><span style=\"color: #00add2;\"><span class=\"cerna0\">Kohout, M.;<\/span><\/span><\/span> <\/span>C<\/span>ibulka, R.:<\/span><\/span> <br \/>Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light <br \/><em><span lang=\"EN-GB\">Org. Biomol. Chem. <\/span><\/em><span lang=\"EN-GB\"><strong>2017<\/strong><\/span><em><span lang=\"EN-GB\">, 15, <\/span><\/em><span lang=\"EN-GB\">1970-1975<\/span><span lang=\"EN-GB\">\u00a0DOI<\/span><span lang=\"EN-GB\">:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6OB02770A\">10.1039\/C6OB02770A<\/a><\/span><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<h3>2016<\/h3>\r\n<ul>\r\n<li>Bajzikova, K.; Kohout, M.; Tarabek, J.; Svoboda, J.; Novotna, V.; Vejpravova, J.; Pociecha, D.; Gorecka, E.:<br \/>All-organic liquid crystalline radicals with a spin unit in the outer position of a bent-core system<br \/><em>J. Mater. Chem. C<\/em> <span class=\"cerna0\"><strong>2016<\/strong>, <em>4<\/em>, 11540-11547<\/span> DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6TC04346A \">10.1039\/C6TC04346A <\/a><br \/><br \/><\/li>\r\n<li>T\u016fma, J.; Kohout, M.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.:<br \/>Bent-core liquid crystals based on 6-substituted 3-hydroxybenzoic acid: the role of substitution and linkage group orientation on mesomorphic properties<br \/><em>Liq. Cryst.<\/em> <strong>2016<\/strong>, <em>43<\/em>, 1889-1900\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1230789\">10.1080\/02678292.2016.1230789<\/a><br \/><br \/><\/li>\r\n<li>Kohout, M.; Vandenbussche, J.; Roller, A.; T\u016fma, J.; Boqaerts, J.; Bultinck, P.; Herrebout, W.; Lindner, W.:<br \/>Absolute configuration of the antimalarial <em>erythro<\/em>-mefloquine - vibrational dichroism and X-ray diffraction studies of mefloquine and its thiourea derivative<br \/><em>RSC Advances<\/em> <strong>2016<\/strong>, <em>6<\/em>, 81461-81465 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C6RA19367F \">10.1039\/C6RA19367F<\/a><span class=\"DOILink\">\u00a0<\/span><br \/><br \/><\/li>\r\n<li>Kohout, M.; Bubnov, A.; \u0160\u0165urala, J.; Novotn\u00e1, V.; Svoboda, J.:<br \/>Effect on alkyl chain length in the terminal ester group on mesomorphic properties of new chiral lactic acid derivatives<br \/><em>Liq. Cryst.<\/em> <strong>2016<\/strong>, <em>43<\/em>,\u00a01472-1485\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2016.1185170\">10.1080\/02678292.2016.1185170<\/a><br \/><br \/><\/li>\r\n<li>Grecs\u00f3, N.; Kohout, M.; Carotti, A.; Sardella, R.; Natalini, B.; F\u00fcl\u00f6p, F.; Lindner, W.; P\u00e9ter, A.; Ilisz, I.:\u00a0<br \/>Mechanistic considerations of enantiorecognition on novel Cinchona alkaloid-based zwitterionic chiral stationary phases from the aspect of the separation of trans-paroxetine enantiomers as model compounds<br \/><em>J. Pharm. Biomed. Anal.<\/em><strong> 2016<\/strong>, <em>124<\/em>,\u00a0164-173 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jpba.2016.02.043\">10.1016\/j.jpba.2016.02.043<\/a><br \/><br \/><\/li>\r\n<li>Wolrab, D.; Fr\u00fchauf, P.; Moulisova, A.; Kuchar, M.; Gerner, C.; Lindner, W.; Kohout, M.:<br \/>Chiral separation of new designer drugs (Cathinones) on chiral ion-exchange type stationary phases<br \/><em>J. Pharm. Biomed. Anal.<\/em><strong> 2016<\/strong>, <em>120<\/em>, 306-315 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.jpba.2015.12.023\" target=\"doilink\" id=\"ddDoi\" class=\"S_C_ddDoi\">10.1016\/j.jpba.2015.12.023<\/a><br \/><br \/><\/li>\r\n<li><span class=\"zelena0\"><span class=\"cerna0\"><span class=\"cerna0\"><span class=\"\">T\u016fma, J.; Kohout, M.; Svoboda, J.<\/span>;<\/span> Novotn\u00e1, V.; Pociecha, D.:\u00a0<br \/>Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core - Part II\u00a0<br \/><em>Liq. Cryst.<\/em> <strong>2016<\/strong>, <em>43<\/em>, 547-563\u00a0DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2015.1125535\">10.1080\/02678292.2015.1125535<br \/><br \/><\/a><\/span><\/span><\/li>\r\n<li><span class=\"zelena0\"><span class=\"cerna0\">Slavik, P.; Kohout, M.; B\u00f6hm, S.; Eigner, V.; Lhotak, P.: <br \/>Synthesis of\u00a0<\/span><\/span>Inherently Chiral Calixarenes via Direct Mercuration of the Partial Cone Conformation\u00a0<br \/><em>Chem. Comm.<\/em> <strong>2016<\/strong>, <em>52<\/em>, 2366-2360\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C5CC09388K\">10.1039\/C5CC09388K<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<h3>2015<\/h3>\r\n<ul>\r\n<li>Tri\u0161ovi\u0107, N.; Antanasijevi\u0107, J.; T\u00f3th-Katona, T.; Kohout, M.; Salamonczyk, M.; Sprunt, S.; J\u00e1kli, A.; Fodor-Csorba, K.: Azo-containing asymmetric bent-core liquid crystals with modulated smectic phase <em>RSC Adv.<\/em> <strong>2015<\/strong>, <em>5<\/em>, 64886-64891. DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1039\/c5ra09764a\">10.1039\/c5ra09764a<\/a><br \/>\u00a0<\/li>\r\n<li>Kohout, M.; Bielec, B.; Steindl, P.; Trettenhahn, G.; Lindner, W.: Mechanistic aspects of the direct C-acylation of cyclic 1,3-diones with various unactivated carboxylic acids <em>Tetrahedron<\/em> <strong>2015<\/strong>, <em>71<\/em>, 2698-2707. DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tet.2015.03.037\" target=\"doilink\" id=\"ddDoi\" class=\"S_C_ddDoi\">10.1016\/j.tet.2015.03.037<\/a><br \/>\u00a0<\/li>\r\n<li>von Koschitzky, I.; Gerhardt, H.; L\u00e4mmerhofer, M.; Kohout, M.; Gehringer, M.; Laufer, S.; Pink, M.; Schmitz-Spanke, S.; Strube, C.; Kaiser, A.: New insights into novel inhibitors against deoxyhypusine hydrolase from plasmodium falciparum: compounds with an iron chelating potential <em>Amino Acids<\/em> <strong>2015<\/strong>, <em>47<\/em>, 1155-1166. DOI: <a href=\"http:\/\/dx.doi.org\/10.1007\/s00726-015-1943-z\">10.1007\/s00726-015-1943-z<\/a><br \/>\u00a0<\/li>\r\n<li>Kohout, M.; Kozm\u00edk, V.; Slabochov\u00e1, M.; T\u016fma, J.; Svoboda, J.; Novotn\u00e1, V.; Pociecha, D.: Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core\u00a0<em>Liq. Cryst.<\/em> <strong>2015<\/strong>, <em>42<\/em>, 87-103. DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1080\/02678292.2014.965232\">10.1080\/02678292.2014.965232<\/a><br \/>\u00a0<\/li>\r\n<li>Kozm\u00edk, V.; Poznik, M.; Svoboda, J.; Frere, P.:<br \/>Dithieno[3,2-b:2',3'-d]furan as a new building block for fused conjugated systems<br \/><em>Tetrahedron Lett.<\/em>\u00a0<strong>2015<\/strong>,\u00a0<em>56<\/em>, 6251-6253.\u00a0<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.09.107\">DOI:10.1016\/j.tetlet.2015.09.107<br \/><\/a>\u00a0<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2015.09.107\"><br \/><\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<p><\/p>\r\n<h3 id=\"r14\" class=\"podnadpis\" style=\"text-align: justify;\"><strong>2014<\/strong><\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Lo Ch., Doucoure B. I., Aaron J.-J., Svoboda J., Kozm\u00edk V., Brochon J.-C., Henry H., Capochichi M.: Synthesis and optical properties of new fluorescent substituted thieno[3,2-b]indole derivatives. <em>Spectrochim. Acta A, Molecular and Biomolecular Spectroscopy<\/em> <strong>2014<\/strong>,<em> 120C<\/em>, 47-54. DOI: <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S1386142513011414\" class=\"text-button\">10.1016\/j.saa.2013.09.134<br \/><\/a>\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S1386142513011414\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Kov\u00e1\u0159ov\u00e1 A., Sv\u011btl\u00edk S., Kozm\u00edk V., Svoboda J., Novotn\u00e1 V., Pociecha D., Gorecka E., Podoliak N.: Unusual polymorphism in new bent-shaped liquid crystals with hydroxybiphenylcarboxylic acid central unit.<em> Beil. J. Org. Chem.<\/em> <strong>2014<\/strong>, <em>10<\/em>, 794-807. DOI: 10.3762\/bjoc.10.75<br \/>\u00a0\u00a0<\/li>\r\n<li>Ol\u0161inov\u00e1 M., Jurkiewicz P., Pozn\u00edk M., \u0160achl R., Prausov\u00e1 T., Hof M., Kozm\u00edk V., Tepl\u00fd F., Svoboda J., Cebecauer M.: Di- and tri-oxalkyl derivatives of boron dipyrromethene (BODIPY) rotor dye in lipid bilayers. <em>PhysChemChemPhys.<\/em> <strong>2014<\/strong>, <em>16<\/em>, 10688-10697. DOI: <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/cp\/c4cp00888j#%21divAbstract\" class=\"text-button\">10.1039\/C4CP00888J<br \/><\/a>\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/cp\/c4cp00888j#%21divAbstract\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Hetteger H., Kohout M., Mimini V., Lindner W.: Novel carbamoyl type quinine and quinidine based chiral anion exchangers implementing alkyne-azide cycloaddition immobilization chemistry. <em>J. Chromatogr. A<\/em> <strong>2014<\/strong>, <em>1337<\/em>, 85-94. DOI: <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0021967314002568\" class=\"text-button\">10.1016\/j.chroma.2014.02.026<\/a><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r13\" class=\"podnadpis\" style=\"text-align: justify;\"><strong>2013<\/strong><\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Machara A., Svoboda J.: Thiophenium-ylides: synthesis and reactivity. <em>Chem. Papers<\/em> <strong>2013<\/strong>, <em>67<\/em>, 59-65. DOI: <a href=\"http:\/\/link.springer.com\/article\/10.2478\/s11696-012-0222-7\" class=\"text-button\">10.2478\/s11696-012-0222-7<br \/><\/a>\u00a0<a href=\"http:\/\/link.springer.com\/article\/10.2478\/s11696-012-0222-7\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Kohout M., T\u016fma J., Svoboda J., Novotn\u00e1 V., Gorecka E., Pocicha D.: 3-Hydroxycinnamic acid - a new central core for the design of bent-shaped liquid crystals. <em>J. Mater. Chem. C<\/em> <strong>2013<\/strong>, <em>1<\/em>, 4962-4969. DOI: <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/tc\/c3tc30664j#%21divAbstract\" class=\"text-button\">10.1039\/C3TC30664J<br \/><\/a>\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/tc\/c3tc30664j#%21divAbstract\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Novotn\u00e1 V., Baumeister U., Kohout M., Svoboda J.: Mesomorphic properties of a bent-shaped liquid crystalline monomer. <em>Phase Trans.<\/em> <strong>2013<\/strong>, <em>86<\/em>, 503-515. DOI: <a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/01411594.2012.702279#.Ur1zGvTuLT8\" class=\"text-button\">10.1080\/01411594.2012.702279<br \/><\/a>\u00a0<a href=\"http:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/01411594.2012.702279#.Ur1zGvTuLT8\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Hor\u010dic M., Kozm\u00edk V., Svoboda J., Novotn\u00e1 V., Pociecha D.: Transformation from a rod-like to a hockey-stick-like and bent-shaped molecule in 3,4'-disubstituted azobenzene-based mesogens. J. Mater. Chem. C 2013, 1, 7560-7567. DOI: <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/tc\/c3tc31593b#%21divAbstract\" class=\"text-button\">10.1039\/C3TC31593B<br \/><\/a>\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/tc\/c3tc31593b#%21divAbstract\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Seidler A., Svoboda J., Dekoj V., Chocholou\u0161ov\u00e1 J., Vacek J., Star\u00e1 I. G., Star\u00fd I.: The synthesis of pi-electron molecular rods with a thiophene or thieno[3,2-b]thiophene core units and sulphur alligator clips. <em>Tetrahedron Lett.<\/em> <strong>2013<\/strong>, <em>54<\/em>, 2795-2798. DOI: <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403913004875\" class=\"text-button\">10.1016\/j.tetlet.2013.03.084<br \/><\/a>\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403913004875\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Novotn\u00e1 V., Glogarov\u00e1 M., Kozm\u00edk V., Svoboda J., Hamplov\u00e1 V., Ka\u0161par M., Pociecha D.: Frustrated phases induced in binary mixtures of hockey-stick and chiral rod-like mesogens. <em>Soft Matter<\/em> <strong>2013<\/strong>, <em>9<\/em>, 647-653. DOI: <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/sm\/c2sm27194j#%21divAbstract\" class=\"text-button\">10.1039\/C2SM27194J<br \/><\/a>\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/sm\/c2sm27194j#%21divAbstract\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Wolrab D., Mac\u00edkov\u00e1 P., Boras M., Kohout M., Lindner W.: Strong cation exchange chiral stationary phase - A comparative study in high-performance liquid chromatography and subcritical fluid chromatography. <em>J. Chromatogr. A<\/em><strong> 2013<\/strong>, <em>1317<\/em>, 59-66. DOI: <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0021967313012892\" class=\"text-button\">10.1016\/j.chroma.2013.08.037<br \/><\/a>\u00a0<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0021967313012892\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Gargano A. F. G., Buchinger S., Kohout M., Lindner W., L\u00e4mmerhofer M.: Single-step Ugi multicomponent reaction for the synthesis of phosphopeptidomimetics. <em>J. Org. Chem.<\/em> <strong>2013<\/strong>, <em>78<\/em>, 10077-10087. DOI: <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo401372x\" class=\"text-button\">10.1021\/jo401372x<br \/><\/a>\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jo401372x\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Wernisch S., Bisi F., Cazzato A. S., Kohout M., Lindner W.: 2-Acyl-dimedones as UV-active protective agents for amino acids: enantiomer separations of the derivatives on chiral anion exchangers. <em>Anal. Bioanal. Chem.<\/em><strong> 2013<\/strong>, <em>405<\/em>, 8011-8026. DOI: <a href=\"http:\/\/link.springer.com\/article\/10.1007\/s00216-013-6932-z\" class=\"text-button\">10.1007\/s00216-013-6932-z<br \/><\/a>\u00a0<a href=\"http:\/\/link.springer.com\/article\/10.1007\/s00216-013-6932-z\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Gargano A. F. G., Kohout M., Mac\u00edkov\u00e1 P., L\u00e4mmerhofer M., Lindner W.: Direct high-performance liquid chromatographic separation of free alpha-, beta- and gamma-aminophosphonic acids employing cinchona-based chiral zwitterionic ion exchangers. <em>Anal. Bioanal. Chem.<\/em> <strong>2013<\/strong>, <em>405<\/em>, 8027-8038. DOI: <a href=\"http:\/\/link.springer.com\/article\/10.1007\/s00216-013-6938-6\" class=\"text-button\">10.1007\/s00216-013-6938-6<br \/><\/a>\u00a0<a href=\"http:\/\/link.springer.com\/article\/10.1007\/s00216-013-6938-6\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Wolrab D., Fr\u00fchauf P., Kohout M., Lindner W.: Click chemistry immobilization strategies in the development of strong cation exchanger chiral stationary phases for HPLC. <em>J. Sep. Sci.<\/em> <strong>2013<\/strong>, <em>36<\/em>, 2826-2837. DOI: <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/jssc.201300559\/abstract\" class=\"text-button\">10.1002\/jssc.201300559<br \/><\/a>\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/jssc.201300559\/abstract\" class=\"text-button\"><br \/><\/a><\/li>\r\n<li>Wolrab D., Kohout M., Boras M., Lindner W.: Strong cation exchange-type chiral stationary phase for enantiseparation of chiral amines in subcritical fluid chromatography. <em>J. Chromatogr. A<\/em> <strong>2013<\/strong>, <em>1289<\/em>, 94-104. DOI: <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0021967313004561\" class=\"text-button\">10.1016\/j.chroma.2013.03.018<\/a><\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r12\" class=\"podnadpis\" style=\"text-align: justify;\">2012<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Mallet C., Savitha G., Allain M., Kozm\u00edk V., Svoboda J., Fre?re P., Roncali J.: Synthesis and electronic properties of D-A-D triads based on 3-alkoxy-4-cyanothiophene and benzothienothiophene blocks. J. Org. Chem. 2012, 77, 2041-2046.<\/li>\r\n<li>Kov\u00e1\u0159ov\u00e1 A., Kozm\u00edk V., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M., Pociecha D.: Naphthalene-based bent-shaped liquid crystals with a semifluorinated terminal chain. Liq. Cryst. 2012, 39, 755-767.<\/li>\r\n<li>Kozm\u00edk V., Hor\u010dic M., Svoboda J., Novotn\u00e1 V., Pociecha D.: 3-Aminophenol based bent-shaped liquid crystals with an amide linking group. Liq. Cryst. 2012, 39, 943-955.<\/li>\r\n<li>Kohout M., K\u00e4hlig H., Wolrab D., Roller A., Lindner W.: Novel chiral selector based on mefloquine - A comparative NMR study to elucidate intermolecular interactions with acidic chiral selectands. Chirality 2012, 24, 936-943.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r11\" class=\"podnadpis\" style=\"text-align: justify;\">2011<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Kohout M., Svoboda J., Novotn\u00e1 V., Pociecha D.: Non-symmetrical bent-shaped liquid crystals based on laterally substituted naphthalene central core with four ester groups. Liq. Cryst. 2011, 38, 1099-1110.<\/li>\r\n<li>Kozm\u00edk V., Henke A., \u0158ehov\u00e1 L., Kurf\u00fcrst M., Slabochov\u00e1 M., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M.: Liquid crystalline benzothiophene derivatives. Part 2. 2,5-Disubstituted benzothiophenes. Liq. Cryst. 2011, 38, 1245-1261.<\/li>\r\n<li>Aaron J.-J., P\u00e1rk\u00e1nyi C., Adenier A.,Potin C., Zaj\u00ed\u010dkov\u00e1 Z., Mart\u00ednez O. R., Svoboda J., Pihera P., V\u00e1chal P.: Fluorescence properties and dipole moments of novel fused thienobenzofurans. Solvent and structural effects. J. Fluorescence 2011, 21, 2133-2141.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r10\" class=\"podnadpis\" style=\"text-align: justify;\">2010<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Kov\u00e1\u0159ov\u00e1 A., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M., Salamonczyk M., Pociecha D., Gorecka E.: [2]Benzothiophene bent-shaped liquid crystals. Liq. Cryst. 2010, 37, 1501-1513.<\/li>\r\n<li>Kozm\u00edk V., Pol\u00e1\u0161ek P., Seidler A., Kohout M., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M., Pociecha D.: The effect of a thiophene ring in the outer position on mesomorphic properties of the bent-shaped liquid crystals. J. Mater. Chem. 2010, 20, 7430-7435.<\/li>\r\n<li>Kohout M., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M., Pociecha D.: Non-symmetrical bent-shaped liquid crystals with five ester groups. Liq. Cryst. 2010, 37, 987-996.<\/li>\r\n<li>Obadovi\u0107 D. \u017d., Vajda A., J\u00e1kli A., Menyh\u00e1rd A., Kohout M., Svoboda J., Stojanovi\u0107 M., \u00c9ber N., Galli G., Fodor-Csorba K.: Mesophase behaviour of binary mixtures of bell-shaped and calamitic compounds. Liq. Cryst. 2010, 37, 527-536.<\/li>\r\n<li>Kohout M., Chambers M., Vajda A., Galli G., Domj\u00e1n A., Svoboda J., Bubnov A., J\u00e1kli A., Fodor-Csorba K.: Properties of non-symmetric bent-core liquid crystals with variable flexible chain length. Liq. Cryst. 2010, 37, 537-545.<\/li>\r\n<li>Ledesma A. E., Contreras C., Svoboda J., Vektariane A., Brand\u00e1n S. A.: Theoretical structures and experimental vibrational spectra of isomeric benzofused thieno[3,2-b]furan compounds. J. Mol. Struc. 2010, 967, 159-165.<\/li>\r\n<li>\u017durek J., Cibulka R., Dvo\u0159\u00e1kov\u00e1 H., Svoboda J.: N1,N10-Ethylene-bridged flavinium salts derived from L-valinol: synthesis and catalytic activity in H2O2 oxidations. Tetrahedron Lett. 2010, 51, 1083-1086.<\/li>\r\n<li>Weissflog W., Pelzl G., Kresse H., Baumeister U., Brand K., Schr\u00f6der M. W., Tamba M. B., Findeisen-Tandel S., Kornek U., Stern S., Eremin A., Stannarius A. , Svoboda J.: In search of a new design strategy for solid single-component organic ferroelectrics: Polar crystalline phases formed by bent-core molecules. J. Mater. Chem. 2010, 20, 6057.<\/li>\r\n<li>L\u00f4 C., Aaron J.-J., Kozm\u00edk V., Svoboda J., Brochon J.-C., Na L.: Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1] benzothiophenes. J. Fluorescence 2010, 20(5), 1037-1047.<\/li>\r\n<li>Glogarov\u00e1 M., Hampl F.,Lej\u010dek L., Novotn\u00e1 V., Svoboda J., Cigl M.: Experimental proof of symmetry breaking in tilted smectics composed of molecules with axial chirality. J. Chem. Phys. 2010, 133, 221102\/1-221102\/4.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r09\" class=\"podnadpis\" style=\"text-align: justify;\">2009<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Kohout M., Svoboda J., Novotn\u00e1 V., Pociecha D., Glogarov\u00e1 M., Gorecka E.: Nematic-polar columnar phase sequence in new bent-shaped liquid crystals based on 7-hydroxynaphthalene-2-carboxylic acid core. J. Mater. Chem. 2009, 19, 3153-3160.<\/li>\r\n<li>Machara J., Kozm\u00edk V., Pojarov\u00e1 M., Dvo\u0159\u00e1kov\u00e1 H., Svoboda J.: Preparation and rearrangement study of novel thiophenium- and selenophenium-ylides. Collect. Czech. Chem. Commun. 2009, 74, 785-798.<\/li>\r\n<li>Vektariene A., Vektaris G., Svoboda J.: A theoretical approach to the nucleophilic behavior of benzofused thieno[3.2-b]furans using DFT and HF based reactivity descriptors. Arkivoc 2009, 311-329.<\/li>\r\n<li>Vaupoti\u0107 N., Szydlowska J., Salamonczyk M., Kov\u00e1\u0159ov\u00e1 A., Svoboda J., Osipov M., Pociecha D., Gorecka E.: Structure studies of the nematic phase formed by bent-core molecules. Phys. Rew. E. 2009, 80, 030701(R)<\/li>\r\n<li>Salamonczyk M., Kov\u00e1\u0159ov\u00e1 A., Svoboda J., Pociecha D., Gorecka E.: Switchable fluorescent liquid crystals. Appl. Phys. Lett. 2009, 95, 171901.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r08\" class=\"podnadpis\" style=\"text-align: justify;\">2008<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Kurf\u00fcrst M., Kozm\u00edk V., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M.: Liquid crystalline benzothiophene derivatives. Liq. Cryst. 2008, 35, 21.<\/li>\r\n<li>Sedl\u00e1k M., Drabina P., L\u00e1nsk\u00fd V., Svoboda J.: Synthesis and characterization of substituted (benzo[b]thiophen-2-yl)-4-methyl-4,5-dihydro-1H-imidazol-5-ones. J. Heterocycl. Chem. 2008, 45, 859.<\/li>\r\n<li>L\u00f4 C., Adenier A., Maurel F., Aaron J.-J., Kozm\u00edk V., Svoboda J..: Electrochemical, spectral and theoretical studies of two new methylthieno[3,2-b]benzothiophenes and their polymers electrosynthesized in organic and micellar media. Synth. Metals 2008, 158, 6-24.<\/li>\r\n<li>Novotn\u00e1 V., \u017durek J., Kozm\u00edk V., Svoboda J., Glogarov\u00e1 M.: Novel hockey-stick mesogens with the nematic, synclinic and anticlinic smectic C phase sequence. Liq. Cryst. 2008, 35, 1023.<\/li>\r\n<li>L\u00f4 C., Aaron J.-J., Svoboda J., Brochon J. C., Na L.: Fluorescence study of new thienobenzothiophene substituted derivatives for luminiscent materials. Luminiscence 2008, 23, 240.<\/li>\r\n<li>Obadovi\u0107 D.Z., Vajda A., J\u00e1kli A., Kohout M., Stojanovi\u0107 M., \u00c9ber N., Fodor-Csorba K., Galli G.: Phase Sequences of Mixtures Formed by Bell-shaped and Calamitic Compound. J. Res. Phys. 2008, 32, 69-74.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r07\" class=\"podnadpis\" style=\"text-align: justify;\">2007<\/h3>\r\n<ul style=\"text-align: justify;\">\r\n<li>Machara A., Pojarov\u00e1 M., Svoboda J.: Synthesis and cycloaddition reaction of 3-vinylthieno[3,2-b][1]benzothiophene. Collect. Czech. Chem. Commun. 2007, 72, 952-964.<\/li>\r\n<\/ul>\r\n<p style=\"text-align: justify;\" class=\"podnadpis\">\u00a0<\/p>\r\n<h3 id=\"r06\" class=\"podnadpis\" style=\"text-align: justify;\">2006<\/h3>\r\n<ul>\r\n<li style=\"text-align: justify;\">Kozm\u00edk V., Kov\u00e1\u0159ov\u00e1 A., Kucha\u0159 M., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M., Kroupa J.: Novel polymerizable bent-shaped monomeric molecules. Liq. Cryst., 2006, 33, 41.<\/li>\r\n<li style=\"text-align: justify;\">Kozm\u00edk V., Ko\u0161ata B., Svoboda J., Kucha\u0159 M.: A study of 5-nitroindole alkylation Collect. Czech. Chem. Commun., 2006, 71, 679.<\/li>\r\n<li style=\"text-align: justify;\">L\u00f4 C., Adenier A., Chane-Ching K., Maurel F., Aaron J. J., Ko\u0161ata B., Svoboda J..: A novel fluorescent, conducting polymer: Poly[1-(thiophene-2-yl)benzothieno[3,2-b]benzothiophene) electrosynthesis, characterization and optical properties. Synth. Metals 2006, 156, 256.<\/li>\r\n<li style=\"text-align: justify;\">\u010cernovsk\u00e1 K., Ko\u0161ata B., Svoboda J., Novotn\u00e1 V., Glogarov\u00e1 M.: Novel ferroelectric liquid crystals based on fused thieno[3,2 b]furan and thieno[3,2 b]thiophene core. Liq. Cryst. 2006, 33, 987.<\/li>\r\n<li style=\"text-align: justify;\">Aaron J.-J., M\u00e9zlov\u00e1 M., Capochichi M., Svoboda J., Brochon J.-C., Guiot E.: Fluorescence properties of new fused thienoindoles and their conductiong oligomers? Evidence for a heavy atom quenching effect. Luminiscence 2006, 21, 330.<\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["38654"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"38654":{"idvazba":"168041","nad_uzel":"136639","pod_uzel":"38654","url":"","sablona":"4","nazev":"Svoboda's Group","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.03.2017 16:57:00","platne_do":null,"iduzel":"38654","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}},"139512":{"idvazba":"171623","nad_uzel":"116995","pod_uzel":"139512","url":"\/research\/tlusty","sablona":"49","nazev":"Supramolecular and reticular chemistry group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tlusty}","poradi":"12","skupina_www":"everyone","platne_od":"29.09.2026 13:27:00","platne_do":null,"iduzel":"139512","obsah":"a:13:{s:5:\"nazev\";s:44:\"Supramolecular and reticular chemistry group\";s:9:\"seo_title\";s:44:\"Supramolecular and reticular chemistry group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:525:\"<p><img src=\"\/images\/0!0\/uzel\/0139512\/0001~~Cy4NSo1PL8ovLQAA.jpg\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\" \u25f3 SuRe_group (jpg) \u2192 (origin\u00e1l)\" width=\"300\" height=\"255\"><\/p>\r\n<p>Our research is focused on the interconnection of supramolecular and reticular chemistry. We use mechanically interlocked molecules such as rotaxanes for the synthesis of porous polymeric materials. In our projects we aim on the improvement of porous material properties by the introduction of the mechanical bond.<\/p>\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","pod_uzly":["147003","148985","147002"],"poduzly_count":3,"poduzly_count_aut":2,"poduzly":{"poduzly_count_aut_sum":0,"147003":{"idvazba":"181451","nad_uzel":"139512","pod_uzel":"147003","url":"\/research\/tlusty\/147003","sablona":"49","nazev":"Financial support","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tlusty\/147003}","poradi":"0","skupina_www":"everyone","platne_od":"09.09.2026 11:53:00","platne_do":null,"iduzel":"147003","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:17:\"Financial support\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"148985":{"idvazba":"183682","nad_uzel":"139512","pod_uzel":"148985","url":"","sablona":"4","nazev":"infobox","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"29.09.2026 13:29:00","platne_do":null,"iduzel":"148985","obsah":"a:8:{s:5:\"nazev\";s:0:\"\";s:8:\"uslideru\";s:5:\"false\";s:10:\"podstranky\";s:4:\"true\";s:12:\"poddokumenty\";s:5:\"false\";s:13:\"urlnadstranka\";s:0:\"\";s:6:\"sticky\";s:0:\"\";s:4:\"text\";s:0:\"\";s:12:\"barva_pozadi\";s:7:\"cervena\";}","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"147002":{"idvazba":"181450","nad_uzel":"139512","pod_uzel":"147002","url":"\/research\/tlusty\/147002","sablona":"49","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tlusty\/147002}","poradi":"2","skupina_www":"everyone","platne_od":"09.09.2026 11:53:00","platne_do":null,"iduzel":"147002","obsah":"a:13:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:5:\"perex\";s:0:\"\";s:5:\"obsah\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:13:\"urlnadstranka\";s:0:\"\";}","class":"stranka_kontejnery","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"136640":{"idvazba":"168063","nad_uzel":"116995","pod_uzel":"136640","url":"\/research\/tobrman","sablona":"1","nazev":"Tobrman's Group","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman}","poradi":"13","skupina_www":"everyone","platne_od":"12.05.2026 21:35:49.13659","platne_do":null,"iduzel":"136640","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:15:\"Tobrman's Group\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:6427:\"<h2><strong>News<br><\/strong><\/h2>\r\n<table class=\"table_bezramecku\" style=\"width: 100%; border-collapse: collapse;\" border=\"1\">\r\n<tbody>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>January 2025<\/strong><\/p>\r\n<p>Tom\u00e1\u0161 Tobrman has been appointed as an editor of <a href=\"https:\/\/link.springer.com\/journal\/11696\" target=\"_blank\" title=\"Chemical Papers\" rel=\"noopener\"><em>Chemical Papers<\/em><\/a>.<\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>December 2024<\/strong><\/p>\r\n<p>Filip Markovi\u010d joined our group.<\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>November 2024<\/strong><\/p>\r\n<p>V\u00e1clav Hron, Denisa Skurkov\u00e1, and Hana Hovorkov\u00e1 secured second place in the bachelor's and master's sections at SVK 2024.<\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>June 2024<\/strong><\/p>\r\n<p>Scarlet Stefanie Vran\u00edk and So\u0148a Pol\u00e1\u010dkov\u00e1 successfully defended their diploma theses.<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>January 2024<\/strong><\/p>\r\n<p>Our contribution to the Science of Synthesis has been published:<\/p>\r\n<p>T. Tobrman, 9.14.5 Phospholes (Update 2024),&nbsp; <em>Science of Synthesis<\/em>, <strong>2024,<\/strong> DOI: <a href=\"https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-109-00525&amp;position=1\">https:\/\/science-of-synthesis.thieme.com\/app\/text\/?id=SD-109-00525&amp;position=1<\/a><\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>October 2023<\/strong><\/p>\r\n<p>Sergej Mrkobrada defended the diploma thesis.<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>June 2023<\/strong><\/p>\r\n<p>Denisa Skurkov\u00e1 defended <span style=\"font-size: 11.0pt; line-height: 107%; font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-font-family: 'Times New Roman'; mso-bidi-theme-font: minor-bidi; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">the bachelor's thesis.<\/span><\/p>\r\n<p class=\"MsoNormal\">One-day river trip from T\u00fdnec nad S\u00e1zavou to Pikovice.<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>February 2023<\/strong><\/p>\r\n<p class=\"MsoNormal\">Zden\u011bk Hartman was admitted to the University of Cambridge. Congratulations!<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>December 2022<\/strong><\/p>\r\n<p class=\"MsoNormal\">In collaboration with Prof. Cibulka\u2019s group, we published the preparation of arylated flavins:<o:p><\/o:p>&nbsp;<\/p>\r\n<p>Marek C\u030cubin\u030c\u00e1k, Naisargi Varma, Petr Oeser, Adam Pokluda, Tetiana Pavlovska, Radek Cibulka,<br>&nbsp;Marek Sikorski, and Tom\u00e1s\u030c Tobrman, Tuning the Photophysical Properties of Flavins by Attaching an Aryl Moiety via Direct C-C Bond Coupling. <em>J. Org. Chem.<\/em> <strong>2022<\/strong>, DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.2c02168\" title=\"DOI URL\">10.1021\/acs.joc.2c02168.<\/a><\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 72px; width: 100%;\">\r\n<p><strong>Autumn 2022<\/strong><\/p>\r\n<p>Andrea Blahovcov\u00e1, Hana Hovorkov\u00e1 and Marek Filippi joined our group.<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 54px; width: 100%;\">\r\n<p><strong>August 2022<\/strong><\/p>\r\n<p>Ale\u0161 Kr\u010dil defended the diploma thesis.<\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 72px; width: 100%;\">\r\n<p><strong>June 2022<\/strong><\/p>\r\n<p>So\u0148a Pol\u00e1\u010dkov\u00e1 a Scarlet Stefanie Vran\u00edk defended the diploma thesis.<\/p>\r\n<p><\/p>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 54px; width: 100%;\">\r\n<p><strong>June2022<\/strong><\/p>\r\n<p>One-day river trip from Vy\u0161\u0161\u00edho Brod to \u010cesk\u00fd Krumlov.<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"height: 18px; width: 100%;\">\r\n<p><strong>June 2022<\/strong><\/p>\r\n<p>Karol\u00edna \u0160ilh\u00e1nov\u00e1 defended <span style=\"font-size: 11.0pt; line-height: 107%; font-family: 'Calibri',sans-serif; mso-ascii-theme-font: minor-latin; mso-fareast-font-family: Calibri; mso-fareast-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-bidi-font-family: 'Times New Roman'; mso-bidi-theme-font: minor-bidi; mso-ansi-language: CS; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;\">the bachelor's thesis<\/span>.<\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>October 2019<\/strong><\/p>\r\n<p>Veronika Budkov\u00e1 a Nikola Studni\u010dkov\u00e1 joined our group.<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>October 2019<\/strong><\/p>\r\n<p>We have published stereoselective synthesis of trisubstituted alkenes:&nbsp;<em>J. Organomet. Chem.<\/em>, Stereoselective synthesis of trisubstituted alkenyl Fischer aminocarbenes through self-mediated \u03b1-haloketone olefination,&nbsp;<a href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2019.120971\">https:\/\/doi.org\/10.1016\/j.jorganchem.2019.120971<\/a><\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054126\/0001~~CwmJz0stLzYwAgA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"162\"><\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>September 2019<\/strong><\/p>\r\n<p>We have published a review on the use of indolylboronic acids in organic synthesis:&nbsp;<em>Molecules<\/em>, Indolylboronic Acids: Preparation and Applications.&nbsp;<strong>2019<\/strong>, 24, 3523.&nbsp;<a href=\"https:\/\/www.mdpi.com\/1420-3049\/24\/19\/3523\">https:\/\/www.mdpi.com\/1420-3049\/24\/19\/3523<\/a><\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>July 2019<\/strong><\/p>\r\n<p>Tereza Edlov\u00e1 created a laboratory logo:<\/p>\r\n<p><img src=\"\/images\/0!0\/uzel\/0054126\/0003~~CwmJz0stLzYwBgA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"320\" height=\"268\"><\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>June 2019<\/strong><br>Peter Polak won the J.-M. Lehn prize for chemistry 2020 and Marek \u010cubi\u0148\u00e1k finished third in the Synthon Award 2019!<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">\r\n<p><strong>January 2019:<\/strong><br>Ale\u0161 Kr\u010dil, Jan Bejbl\u00edk and Karol\u00edna \u0160ilh\u00e1nov\u00e1 joined our group.<\/p>\r\n<p><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 100%;\">&nbsp;<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["54131","136641","54188","136648","136649"],"poduzly_count":5,"poduzly_count_aut":3,"poduzly":{"poduzly_count_aut_sum":6,"54131":{"idvazba":"168046","nad_uzel":"136641","pod_uzel":"54131","url":"","sablona":"4","nazev":"Tobrman's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"27.04.2020 17:21:00","platne_do":null,"iduzel":"54131","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136641":{"idvazba":"168044","nad_uzel":"136640","pod_uzel":"136641","url":"\/research\/tobrman\/people_clone_20415","sablona":"1","nazev":"People","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415}","poradi":"1","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.313475","platne_do":null,"iduzel":"136641","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:6:\"People\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:4936:\"<h2 style=\"text-align: center;\">Current&nbsp;group members<\/h2>\r\n<p><\/p>\r\n<table class=\"table_bezramecku\" style=\"height: 171px;\" width=\"623\">\r\n<tbody>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"height: 19px; width: 205.688px;\">\r\n<h4><strong>Students:<\/strong>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/h4>\r\n<\/td>\r\n<td style=\"height: 19px; width: 158.547px;\">\r\n<h4><strong>PhD students:&nbsp;<\/strong>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/h4>\r\n<\/td>\r\n<td style=\"height: 19px; width: 219.766px;\">\r\n<h4><strong>Assoc. Prof.:<\/strong><\/h4>\r\n<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 205.688px;\">\r\n<ul><\/ul>\r\n<ul><\/ul>\r\n<p>Andrea Blahovcov\u00e1<\/p>\r\n<p><\/p>\r\n<p>Ond\u0159ej Fako<\/p>\r\n<p><\/p>\r\n<p>Marek Filippi<\/p>\r\n<p><\/p>\r\n<p>Hana Hovorkov\u00e1<\/p>\r\n<p><\/p>\r\n<p>V\u00e1clav Hron<\/p>\r\n<p><\/p>\r\n<p>Filip Markovi\u010d<\/p>\r\n<p><\/p>\r\n<p>Denisa Skurkov\u00e1<\/p>\r\n<\/td>\r\n<td style=\"width: 158.547px;\">\r\n<ul>\r\n<li><a href=\"\/research-groups\/tobrman-en\/people\/cubinak\" rel=\"follow\">Marek \u010cubi\u0148\u00e1k<\/a><\/li>\r\n<li><a href=\"\/research-groups\/tobrman-en\/people\/koudelka\" rel=\"follow\">Jakub Koudelka<\/a><\/li>\r\n<li><a href=\"\/research-groups\/tobrman-en\/people\/oeser\" rel=\"follow\">Petr Oeser<\/a><\/li>\r\n<li><a href=\"\/research-groups\/tobrman-en\/people\/petrenko\" rel=\"follow\">Artem Petrenko<\/a><\/li>\r\n<\/ul>\r\n<h4><strong>&nbsp;<\/strong><\/h4>\r\n<\/td>\r\n<td style=\"width: 219.766px;\">\r\n<h4><a href=\"\/research-groups\/tobrman-en\/people\/tobrman\" rel=\"follow\">Tom\u00e1\u0161 Tobrman<\/a><\/h4>\r\n<p>Department of Organic Chemistry<\/p>\r\n<p>UCT Prague<\/p>\r\n<p>Technick\u00e1 5<\/p>\r\n<p>166 28 Praha 6<\/p>\r\n<p>tel: +420 220 444 245<\/p>\r\n<p>fax: +420 220 444&nbsp;288<\/p>\r\n<p><a href=\"mailto:tomas.tobrman@vscht.cz\">tomas.tobrman@vscht.cz<\/a><br><br><\/p>\r\n<p><\/p>\r\n<p><strong>Technician:<\/strong><\/p>\r\n<p>Marta Tok\u00e1rov\u00e1<\/p>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<p><\/p>\r\n<hr>\r\n<h4><strong>Our alumni:<\/strong><\/h4>\r\n<p>&nbsp;<\/p>\r\n<table style=\"height: 625px; width: 806px;\">\r\n<tbody>\r\n<tr style=\"height: 19px;\">\r\n<td style=\"height: 19px; width: 181.75px;\"><strong>PhD students:<\/strong><\/td>\r\n<td style=\"height: 19px; width: 209.859px;\"><strong>Master students:<\/strong><\/td>\r\n<td style=\"height: 19px; width: 186.766px;\"><strong>Bachelor students:<\/strong><\/td>\r\n<td style=\"width: 142.625px;\">\r\n<p><b>Visiting<\/b><b> <\/b><b>students<\/b><b>:<\/b><\/p>\r\n<\/td>\r\n<\/tr>\r\n<tr style=\"height: 551px;\">\r\n<td style=\"height: 551px; width: 181.75px;\">\r\n<ul>\r\n<li><a href=\"\/research-groups\/tobrman-en\/people\/polak\" rel=\"follow\">Peter Pol\u00e1k<\/a> (2020)<\/li>\r\n<li>Vladislav Kotek&nbsp;(2015)<\/li>\r\n<li>Martin K\u0159ov\u00e1\u010dek (2011)<\/li>\r\n<li>Tom\u00e1\u0161 Tobrman (2005)<\/li>\r\n<li>Lud\u011bk Meca (2004)<\/li>\r\n<li>Martina Havelkov\u00e1 (2002)<\/li>\r\n<li>Miroslav Havr\u00e1nek (1998)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<td style=\"height: 551px; width: 209.859px;\">\r\n<ul>\r\n<li>Scarlet Stefanie Vran\u00edk (2024)<\/li>\r\n<li>So\u0148a Pol\u00e1\u010dkov\u00e1 (2024)<\/li>\r\n<li>Sergej Mrkobrada (2023)<\/li>\r\n<li>Karol\u00edna \u0160ilh\u00e1nov\u00e1 (2022)<\/li>\r\n<li>Ale\u0161 Kr\u010dil (2022)<\/li>\r\n<li>Tereza Edlov\u00e1 (2021)<\/li>\r\n<li>Eva Ostapenko (2021)<\/li>\r\n<li>Artem Petrenko (2020)<\/li>\r\n<li>Jakub Koudelka (2020)<\/li>\r\n<li>Petr Oeser (2020)<\/li>\r\n<li>V\u00e1clav Vra\u0161til (2019)<\/li>\r\n<li>Marek \u010cubi\u0148\u00e1k (2018)<\/li>\r\n<li>Eli\u0161ka Fikejzlov\u00e1 (2018)<\/li>\r\n<li>Filip Gracias (2018)<\/li>\r\n<li>Ji\u0159\u00ed Lap\u010d\u00edk (2017)<\/li>\r\n<li>Krist\u00fdna Kolouchov\u00e1 (2016)<\/li>\r\n<li>Luk\u00e1\u0161 Lattenberk (2016)<\/li>\r\n<li>Iegor Vyshnytskyi (2016)<\/li>\r\n<li>Peter Pol\u00e1k (2015)<\/li>\r\n<li>Hana V\u00e1\u0148ov\u00e1 (2015)<\/li>\r\n<li>Petr Koukal (2013)<\/li>\r\n<li>Ivana Jur\u00e1skov\u00e1 (2012)<\/li>\r\n<li>Ivana Nouskov\u00e1 (2011)<\/li>\r\n<li>Ivana Kub\u00ed\u010dkov\u00e1 (2011)<\/li>\r\n<li>Petra Slav\u00edkov\u00e1 (2009)<\/li>\r\n<li>Mark\u00e9ta \u0160m\u00eddkov\u00e1 (2009)<\/li>\r\n<li>Miroslava Tobrmanov\u00e1 (2007)<\/li>\r\n<li>Martin Kle\u010dka (2007)<\/li>\r\n<li>Jaroslav Padev\u011bt (2006)<\/li>\r\n<li>Jana Roh\u00e1\u010dov\u00e1 (2005)<\/li>\r\n<li>Ji\u0159\u00ed \u010cern\u00fd (2002)<\/li>\r\n<li>Du\u0161an Draho\u0148ovsk\u00fd (2000)<\/li>\r\n<li>Ivan Rotrekl (2000)<\/li>\r\n<li>Martin Studenovsk\u00fd (1999)<\/li>\r\n<li>Petr Such\u00fd (1996)<\/li>\r\n<li>Roman W\u00e1gner (1995)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<td style=\"height: 551px; width: 186.766px;\">\r\n<ul>\r\n<li>Denisa Skurkov\u00e1 (2023)<\/li>\r\n<li>Stefanie Scarlet Vran\u00edk (2022)<\/li>\r\n<li>So\u0148a Pol\u00e1\u010dkov\u00e1&nbsp; (2022)<\/li>\r\n<li>Veronika Budkov\u00e1 (2021)<\/li>\r\n<li>Jan Bejbl\u00edk (2020)<\/li>\r\n<li>Ale\u0161 Kr\u010dil (2020)<\/li>\r\n<li>Karol\u00edna \u0160ilh\u00e1nov\u00e1 (2020)<\/li>\r\n<li>Eva Ostapenko (2019)<\/li>\r\n<li>Tereza Edlov\u00e1 (2019)<\/li>\r\n<li>Mat\u00fa\u0161 Drexler (2019)<\/li>\r\n<li>Jakub Koudelka (2018)<\/li>\r\n<li>Petr Oeser (2018)<\/li>\r\n<li>Roman Vale\u0161 (2017)<\/li>\r\n<li>V\u00e1clav Vra\u0161til (2017)<\/li>\r\n<li>Marek \u010cubi\u0148\u00e1k (2016)<\/li>\r\n<li>Eli\u0161ka Fikejzov\u00e1 (2016)<\/li>\r\n<li>Luk\u00e1\u0161 Lattenberk (2014)<\/li>\r\n<li>Hana V\u00e1\u0148ov\u00e1 (2013)<\/li>\r\n<li>Peter Pol\u00e1k (2013)<\/li>\r\n<li>Michal Mary\u0161ka (2012)<\/li>\r\n<li>\u0160\u00e1rka P\u011bchou\u010dkov\u00e1 (2011)<\/li>\r\n<li>Gabriel T\u00f3th (2008)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<td style=\"width: 142.625px;\">\r\n<ul>\r\n<li>Baptiste Chartier (France, 2021)<\/li>\r\n<li>Antoine Catinaud (France, 2019)<\/li>\r\n<\/ul>\r\n<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["136642","54131","136643","136644","136645","136646","136647"],"poduzly_count":7,"poduzly_count_aut":6,"poduzly":{"poduzly_count_aut_sum":0,"136642":{"idvazba":"168045","nad_uzel":"136641","pod_uzel":"136642","url":"\/research\/tobrman\/people_clone_20415\/petrenko_clone_75693","sablona":"1","nazev":"Artem Petrenko","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/petrenko_clone_75693}","poradi":"0","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.33803","platne_do":null,"iduzel":"136642","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:14:\"Artem Petrenko\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:679:\"<h3><strong>Artem Petrenko, MSc.<\/strong><\/h3>\r\n<p><strong>&nbsp;<\/strong>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444 288<br \/><br \/><a href=\"mailto:petrenka@vscht.cz\" rel=\"follow\">petrenka@vscht.cz<\/a><\/p>\r\n<p><strong>PhD thesis:<\/strong><\/p>\r\n<p>C-H activation for the synthesis of functionalized pyrenes<\/p>\r\n<p><strong>Publications:<\/strong><\/p>\r\n<p>Oeser, P., Koudelka, J., Petrenko, A. and Tobrman, T.:<br \/>Recent Progress Concerning the N-Arylation of Indoles.<br \/><em>Molecules <\/em><strong>2021<\/strong>, <em>26<\/em>, 5079.<u> DOI: 10.3390\/molecules2616507<\/u>9<o:p><\/o:p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"54131":{"idvazba":"168046","nad_uzel":"136641","pod_uzel":"54131","url":"","sablona":"4","nazev":"Tobrman's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"27.04.2020 17:21:00","platne_do":null,"iduzel":"54131","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0},"136643":{"idvazba":"168047","nad_uzel":"136641","pod_uzel":"136643","url":"\/research\/tobrman\/people_clone_20415\/koudelka_clone_40793","sablona":"1","nazev":"Jakub Koudelka","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/koudelka_clone_40793}","poradi":"2","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.347484","platne_do":null,"iduzel":"136643","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:14:\"Jakub Koudelka\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1407:\"<h3><strong>Jakub Koudelka, MSc.<\/strong><\/h3>\r\n<p><strong>&nbsp;<\/strong>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444 288<br \/><br \/><a href=\"mailto:jakub.koudelka@vscht.cz\" rel=\"follow\">jakub.koudelka@vscht.cz<\/a><\/p>\r\n<p><strong>PhD thesis:<\/strong><\/p>\r\n<p>Cross-coupling reactions&nbsp; of activated C-O bonds<\/p>\r\n<p><strong>Publications:<\/strong><\/p>\r\n<p>Oeser, P., Koudelka, J., Petrenko, A. and Tobrman, T.:<br \/>Recent Progress Concerning the N-Arylation of Indoles.<br \/><em>Molecules <\/em><strong>2021<\/strong>, <em>26<\/em>, 5079.<span style=\"text-decoration: underline;\"> DOI: 10.3390\/molecules2616507<\/span>9<\/p>\r\n<p>Koudelka, J.; Tobrman, T.:<br \/>Synthesis of 2-Substituted Cyclobutanones by a Suzuki Reaction and Dephosphorylation Sequence.<br \/><em>Eur. J. Org. Chem<\/em>. <strong>2021<\/strong>, 3260-3269. <span style=\"text-decoration: underline;\">DOI:10.1002\/ejoc.202100464<\/span><\/p>\r\n<p>Oeser, P.; Koudelka, J.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T.:<br \/>Formation of trisubstituted buta-1,3-dienes and \u03b1,\u03b2-unsaturated ketones via the reaction of functionalized vinyl phosphates and vinyl phosphordiamidates with organometallic reagents.<br \/><i>RSC <\/i><i>Adv<\/i><i>.<\/i> <b>2020<\/b>, <i>10<\/i>, 35109-35120. DOI: <a href=\"https:\/\/doi.org\/10.1039\/D0RA07472A\" rel=\"follow\">10.1039\/D0RA07472A<\/a><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136644":{"idvazba":"168048","nad_uzel":"136641","pod_uzel":"136644","url":"\/research\/tobrman\/people_clone_20415\/oeser_clone_33748","sablona":"1","nazev":"Petr Oeser","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/oeser_clone_33748}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.355026","platne_do":null,"iduzel":"136644","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:10:\"Petr Oeser\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1346:\"<h3><strong>Petr Oeser, MSc.<\/strong><\/h3>\r\n<p><strong>&nbsp;<\/strong>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444 288<br \/><br \/><a href=\"mailto:petr.oeser@vscht.cz\" rel=\"follow\">petr.oeser@vscht.cz<\/a><\/p>\r\n<p><strong>PhD thesis:<\/strong><\/p>\r\n<p>Cross-coupling reactions of phospholes<\/p>\r\n<p><strong>Publications:<\/strong><\/p>\r\n<p>Oeser, P., Koudelka, J., Petrenko, A. and Tobrman, T.:<br \/>Recent Progress Concerning the N-Arylation of Indoles.<br \/><em>Molecules <\/em><strong>2021<\/strong>, <em>26<\/em>, 5079.<u> DOI: 10.3390\/molecules2616507<\/u>9<o:p><\/o:p><\/p>\r\n<p>Oeser, P., Edlov\u00e1, T., \u010cubi\u0148\u00e1k, M. and Tobrman, T.:<br \/>Transition-Metal-Free Ring-Opening Reaction of 2-Halocyclobutanols through Ring Contraction.<br \/><em>Eur. J. Org. Chem<\/em>. <strong>2021<\/strong>, 4958-4967. <u>DOI: 10.1002\/ejoc.202100837<\/u><o:p><\/o:p><\/p>\r\n<p>Oeser, P.; Koudelka, J.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T.:<br \/>Formation of trisubstituted buta-1,3-dienes and \u03b1,\u03b2-unsaturated ketones via the reaction of functionalized vinyl phosphates and vinyl phosphordiamidates with organometallic reagents.<br \/><i>RSC <\/i><i>Adv<\/i><i>.<\/i> <b>2020<\/b>, <i>10<\/i>, 35109-35120. DOI: <a href=\"https:\/\/doi.org\/10.1039\/D0RA07472A\" rel=\"follow\">10.1039\/D0RA07472A<\/a><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136645":{"idvazba":"168049","nad_uzel":"136641","pod_uzel":"136645","url":"\/research\/tobrman\/people_clone_20415\/polak_clone_16040","sablona":"1","nazev":"Peter Pol\u00e1k","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/polak_clone_16040}","poradi":"4","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.400615","platne_do":null,"iduzel":"136645","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Peter Pol\u00e1k\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:4160:\"<h3><strong><img src=\"\/images\/215!0\/uzel\/0054486\/0001~~K8jPScwGAA.jpg\" class=\"img_float_left img_fancy_no\" alt=\"\" width=\"215\" height=\"322\" \/>Dr. Peter Pol\u00e1k<\/strong><\/h3>\r\n<p><strong>\u00a0<\/strong><\/p>\r\n<p>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444 288<br \/><br \/><a href=\"mailto:peter.polak@vscht.cz\">peter.polak@vscht.cz<\/a><\/p>\r\n<p><strong><br \/><br \/><br \/><br \/><br \/><br \/><br \/><br \/><br \/>PhD thesis:<\/strong><\/p>\r\n<p>Bromoenol-phosphates as building blocks for regioselective synthesis of functionalized alkenes<\/p>\r\n<p><strong>\u00a0<\/strong><\/p>\r\n<p><strong>Publications:<\/strong><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; \u010cejka, J.; Tobrman, T.:<br \/>Formal Transition-Metal-Catalyzed Phosphole C\u2013H Activation for the Synthesis of Pentasubstituted Phospholes.<br \/><em>Org. Lett. <\/em><strong>2020<\/strong>, <em>22<\/em>, 2187\u25002190. DOI: 10.1021\/acs.orglett.0c00359<\/p>\r\n<p>\u00a0Tobrman, T; Krupi\u010dka, M.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; \u010cubi\u0148\u00e1k, M.; Babor, M.; Dvo\u0159\u00e1k, D.:<br \/>Diastereoselective Cyclopropanation through Michael Addition\u2010Initiated Ring Closure between \u03b1,\u03b1\u2010Dibromoketones and \u03b1,\u03b2\u2010Unsaturated Fischer Carbene Complexes.<br \/><em>Eur. J. Org. Chem.<\/em> <strong>2020<\/strong>, 429\u2500436. DOI: 10.1002\/ejoc.201901503<\/p>\r\n<p>\u00a0\u010cubi\u0148\u00e1k, M.; Edlov\u00e1, T.; Pol\u00e1k, P.; Tobrman, T.: Indolylboronic Acids: Preparation and Applications.<br \/><em>Molecules<\/em>\u00a0<strong>2019<\/strong>, 24, 3523. DOI:\u00a0<a href=\"https:\/\/doi.org\/10.3390\/molecules24193523\">10.3390\/molecules24193523<\/a><\/p>\r\n<p>\u00a0Tobrman, T.; Pol\u00e1k, P.; \u010cubi\u0148\u00e1k, M.; Dvo\u0159\u00e1kov\u00e1, H.; Dvo\u0159\u00e1k, D.: Dichotomy within 1,4-addition of organolithium and Grignard reagents to \u03b1,\u03b2-unsaturated Fischer alkoxycarbenes: A new synthesis of Fischer carbenes.<br \/><em>Tetrahedron<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em>75<\/em>, 2175-2181. DOI:\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.tet.2019.02.038\">10.1016\/j.tet.2019.02.038<\/a><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; Tobrman, T.: Novel Selective Approach to Terminally Substituted [n]Dendralenes<br \/><em>Eur. J. Org. Chem.\u00a0<\/em><strong>2019<\/strong>, 957-968.\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201801522\">10.1002\/ejoc.201801522<\/a><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; Dvo\u0159\u00e1k, D.; Tobrman, T.:<br \/>Cyanogen: A Versatile Reagent for Diversity-Oriented Synthesis<br \/><em>Synthesis<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>49<\/em>, 1757-1766. DOI:<a href=\"http:\/\/dx.doi.org\/10.1055\/s-0036-1588410\">10.1055\/s-0036-1588410<\/a><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; Tobrman, T.:<br \/>The synthesis of polysubstituted indoles from 3-bromo-2-indolyl phosphates<br \/><em>Org. Biomol. Chem.<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>15<\/em>, 6233-6241. DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7OB01127J\">10.1039\/C7OB01127J<\/a><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; Tobrman, T.:<br \/>Dearomatization Strategy for the Synthesis of Arylated 2H-Pyrroles and 2,3,5-Trisubstituted 1H-Pyrroles.<br \/><em>Org. Lett.<\/em><strong>\u00a02017<\/strong>,\u00a0<em>19<\/em>, 460-4611. DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b02219\">10.1021\/acs.orglett.7b02219<\/a><\/p>\r\n<p>Kotek, V.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T.:<br \/>Aluminium Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues.<br \/><em>Eur. J. Org. Chem.<\/em>\u00a0<strong>2016<\/strong>, 5037-5044.\u00a0DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201600959\">10.1002\/ejoc.201600959<\/a><\/p>\r\n<p>\u00a0Pol\u00e1k, P.; V\u00e1\u0148ov\u00e1, H.; Dvo\u0159\u00e1k, D.; Tobrman, T.:<br \/>Recent Progress in Transition Metal-Catalyzed Stereoselective Synthesis of Acyclic All-Carbon Tetrasubstituted Alkenes.<br \/><em>Tetrahedron Lett.<\/em>\u00a0<strong>2016<\/strong>,\u00a0<em>57<\/em>, 3684-3693 DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2016.07.030\">10.1016\/j.tetlet.2016.07.030<\/a>\u00a0<\/p>\r\n<p>\u00a0Kotek, V.;\u00a0Pol\u00e1k, P.;\u00a0Tobrman, T.:\u00a0<br \/>Efficient and Simple Preparation of Functionalized 1,1-Dibromoenol Phosphates\u00a0<br \/><em>Monatshefte fuer Chemie<\/em>\u00a0<strong>2016<\/strong>,\u00a0<em>147<\/em>, 405-412. DOI:<a href=\"http:\/\/dx.doi.org\/10.1007\/s00706-015-1613-6\">10.1007\/s00706-015-1613-6<\/a><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136646":{"idvazba":"168050","nad_uzel":"136641","pod_uzel":"136646","url":"\/research\/tobrman\/people_clone_20415\/tobrman_clone_50194","sablona":"1","nazev":"Tom\u00e1\u0161 Tobrman","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/tobrman_clone_50194}","poradi":"5","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.420381","platne_do":null,"iduzel":"136646","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:15:\"Tom\u00e1\u0161 Tobrman\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:1755:\"<h3><img src=\"\/images\/215!0\/uzel\/0054481\/0001~~C8lPKspNzAMA.jpg\" class=\"img_float_left img_fancy_no\" alt=\"\" width=\"215\" height=\"287\" \/><br \/>Assoc. Prof. Tom\u00e1\u0161 Tobrman<\/h3>\r\n<p>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444\u00a0288<br \/><br \/><\/p>\r\n<p><a href=\"mailto:tomas.tobrman@vscht.cz\">tomas.tobrman@vscht.cz<\/a><\/p>\r\n<p><br \/><br \/><\/p>\r\n<p><strong><br \/><br \/>Date and place of birth<\/strong><\/p>\r\n<p>22.11. 1977, Plze\u0148<\/p>\r\n<p>\u00a0<\/p>\r\n<p><strong>Work Experience\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong><\/p>\r\n<p>2015\u2013today: Associate professor at the Department of Organic Chemistry, UCT Prague.<\/p>\r\n<p>2005\u20132014: Assistant professor at the Department of Organic Chemistry, UCT Prague.<\/p>\r\n<p>22.1. 2008\u201330.6. 2009: Post-doc position in the group of prof. E.-i. Negishi, Purdue University, In, USA, Subject: Alkyne haloboration: An Application in stereoselective synthesis of trisubstituted alkenes.<\/p>\r\n<p>15.9. 2004 \u2013 28.2. 2005: Research in the group of prof. Tobias Rein, KTH, Stockholm, Sweden<br \/>Subject: Asymetric Wittig reaction<\/p>\r\n<p>\u00a0<\/p>\r\n<p><strong>Education and training<\/strong><\/p>\r\n<p>\u00a02001-2005: PhD study at the UCT Prague (Czech Republic), Subject: Modification of purine ring by utilization of reactivity of transition metals<\/p>\r\n<p>4.-20. 7. 2001: 101<sup>st<\/sup> International summer course, BASF, Ludwigshafen (Germany)<\/p>\r\n<p>1996-2001: UCT Prague (Czech Republic)<\/p>\r\n<p>Diploma Thesis: Chelated( h<sup>2<\/sup>-allylamino)carbene complexes of iron, chromium and tungsten: Preparation and properties<\/p>\r\n<p>1992-1996: High school, MS\u0160CH, Prague (Czech Republic)<\/p>\r\n<p><br \/><br \/><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0},"136647":{"idvazba":"168051","nad_uzel":"136641","pod_uzel":"136647","url":"\/research\/tobrman\/people_clone_20415\/cubinak_clone_38504","sablona":"1","nazev":"Marek \u010cubi\u0148\u00e1k","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/people_clone_20415\/cubinak_clone_38504}","poradi":"6","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.429385","platne_do":null,"iduzel":"136647","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:16:\"Marek \u010cubi\u0148\u00e1k\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:3471:\"<h3><strong>Marek \u010cubi\u0148\u00e1k, MSc.<\/strong><\/h3>\r\n<p><strong>&nbsp;<\/strong>Department of Organic Chemistry<br \/>UCT Prague<br \/>Technick\u00e1 5<br \/>166 28 Praha 6<br \/>tel: +420 220 444 245<br \/>fax: +420 220 444 288<br \/><br \/><a href=\"mailto:marek.cubinak@vscht.cz\">marek.cubinak@vscht.cz<\/a><\/p>\r\n<p><strong>PhD thesis:<\/strong><\/p>\r\n<p>Stereoselective synthesis of tetrasubstituted alkenes.<\/p>\r\n<p><strong>Publications:<\/strong><\/p>\r\n<p>Oeser, P., Edlov\u00e1, T., \u010cubi\u0148\u00e1k, M. and Tobrman, T.:<br \/>Transition-Metal-Free Ring-Opening Reaction of 2-Halocyclobutanols through Ring Contraction.<br \/><em>Eur. J. Org. Chem<\/em>. <strong>2021<\/strong>, 4958-4967. <span style=\"text-decoration: underline;\">DOI: 10.1002\/ejoc.202100837<\/span><\/p>\r\n<p>\u010cubi\u0148\u00e1k, M,. Bigeon, J., Gal\u00e1\u0159, P., Ondi\u010d, L. and Tobrman, T.:<br \/>The Synthesis of Tetrasubstituted Cycloalkenes Bearing \u03c0-Conjugated Substituents and Their Optical Properties.<br \/><em>ChemistrySelect<\/em> <strong>2021<\/strong>, 6, 9904-9910. <span style=\"text-decoration: underline;\">DOI: 10.1002\/slct.202103122<\/span><\/p>\r\n<p>Edlov\u00e1, T.; \u010cubi\u0148\u00e1k, M.; Tobrman, T.:&nbsp;<br \/>Cross-Coupling Reactions of Double or Triple Electrophilic Templates for Alkene Synthesis.&nbsp;<br \/><i>Synthesis<\/i> <b>2021<\/b>, <i>53<\/i>, 255-266. DOI: <a href=\"https:\/\/doi.org\/10.1055\/s-0040-1707270\" rel=\"follow\">10.1055\/s-0040-1707270<\/a><\/p>\r\n<p>\u010cubi\u0148\u00e1k, M.; Tobrman, T.:<br \/>Room-Temperature Negishi Reaction of Trisubstituted Vinyl Phosphates for the Synthesis of Tetrasubstituted Alkenes.<br \/><i>J. Org<\/i><i>. <\/i><i>Chem<\/i><i>.<\/i> <b>2020<\/b>, <i>85<\/i>, 10728-10739. DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.0c01254\" rel=\"follow\">10.1021\/acs.joc.0c01254<\/a><br \/><br \/>Tobrman, T.; Krupi\u010dka, M.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; \u010cubi\u0148\u00e1k, M.; Babor, M. ; Dvo\u0159\u00e1k, D.:&nbsp;Diastereoselective Cyclopropanation through Michael Addition\u2010Initiated Ring Closure between \u03b1,\u03b1\u2010Dibromoketones and \u03b1,\u03b2\u2010Unsaturated Fischer Carbene Complexes.<br \/><em>Eur. J. Org. Chem.<\/em> <strong>2020<\/strong>, 429-436. DOI: 10.1002\/ejoc.201901503<\/p>\r\n<p>Tobrman, T.; \u010cubi\u0148\u00e1k, M.; Dvo\u0159\u00e1k, D.: Stereoselective synthesis of trisubstituted alkenyl Fischer aminocarbenes through self-mediated \u03b1-haloketone olefination.<br \/><em>J. Organomet. <\/em><em>Chem.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;902, 120971. DOI <a href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2019.120971\">10.1016\/j.jorganchem.2019.120971<\/a><\/p>\r\n<p>\u010cubi\u0148\u00e1k, M.; Edlov\u00e1, T.; Pol\u00e1k, P.; Tobrman, T.: Indolylboronic Acids: Preparation and Applications.<br \/><em>Molecules<\/em>&nbsp;<strong>2019<\/strong>, 24, 3523 DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.3390\/molecules24193523\">10.3390\/molecules24193523<\/a><\/p>\r\n<p>Tobrman, T.; Pol\u00e1k, P.; \u010cubi\u0148\u00e1k, M.; Dvo\u0159\u00e1kov\u00e1, H.; Dvo\u0159\u00e1k, D.: Dichotomy within 1,4-addition of organolithium and Grignard reagents to \u03b1,\u03b2-unsaturated Fischer alkoxycarbenes: A new synthesis of Fischer carbenes.<br \/><em>Tetrahedron<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>75<\/em>, 2175-2181. DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1016\/j.tet.2019.02.038\">10.1016\/j.tet.2019.02.038<\/a><\/p>\r\n<p>\u010cubi\u0148\u00e1k, M.; Eigner, V.; Tobrman, T.: Bench\u2010Stable Sulfoxide\u2010Based Boronates: Preparation and Application in a Tandem Suzuki Reaction. <br \/><em>Adv. Synth. Catal<strong>.<\/strong><\/em><strong>&nbsp;2018,<\/strong>&nbsp;360, 4604-4614. DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/adsc.201801000\">10.1002\/adsc.201801000<\/a><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","poduzly_count":0,"poduzly_count_aut":0}}},"54188":{"idvazba":"168052","nad_uzel":"136640","pod_uzel":"54188","url":"","sablona":"20","nazev":"Slider","_url_prefix":null,"poradi":"2","skupina_www":"everyone","platne_od":"30.04.2020 20:42:38.967556","platne_do":null,"iduzel":"54188","obsah":null,"class":"slider","autonomni":"0","pod_uzly":["54189"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"54189":{"idvazba":"62740","nad_uzel":"54188","pod_uzel":"54189","url":"","sablona":"20","nazev":"slider","_url_prefix":null,"poradi":"0","skupina_www":"everyone","platne_od":"03.05.2020 19:38:00","platne_do":null,"iduzel":"54189","obsah":"a:8:{s:6:\"nadpis\";s:0:\"\";s:5:\"popis\";s:0:\"\";s:9:\"platne_od\";s:0:\"\";s:9:\"platne_do\";s:0:\"\";s:5:\"odkaz\";s:0:\"\";s:11:\"text_odkazu\";s:0:\"\";s:14:\"obrazek_pozadi\";s:60:\"0003~~O7owMSknPy9RwUhBIzUlsyQ1RcFYz1TPyEDB0NLKxMDK1EATAA.png\";s:11:\"barva_textu\";s:0:\"\";}","class":"slider","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136648":{"idvazba":"168053","nad_uzel":"136640","pod_uzel":"136648","url":"\/research\/tobrman\/research_clone_86147","sablona":"1","nazev":"Research","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/research_clone_86147}","poradi":"3","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.451885","platne_do":null,"iduzel":"136648","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:8:\"Research\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:3814:\"<p>The research activities of our group are focused on the application of the reactivity of transition metals in the following areas:<\/p>\r\n<h2><strong>Design of new reactions and processes for the preparation of heterocyclic compounds<\/strong><\/h2>\r\n<p>Research activities associated with the chemistry of heterocyclic compounds can be demonstrated by the synthesis of pentasubstituted phosphols by copper-catalyzed C-H activation of 1,3,4-trisubstituted phospholes:<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054128\/0001~~CwmJz0stLzYwBAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"211\" \/><\/p>\r\n<p>Pol\u00e1k, P.; Tobrman, T. Formal Transition-Metal-Catalyzed Phosphole C\u2013H Activation for the Synthesis of Pentasubstituted Phospholes. <br \/><em>Org. Lett.<\/em> <strong>2020<\/strong>, <em>22<\/em>, 2187-2190. DOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.0c00359\" rel=\"follow\">10.1021\/acs.orglett.0c00359<\/a><\/p>\r\n<p>Another use of transition-metal-catalyzed reactions is represented by the preparation of trisubstituted pyrroles using a dearomatization strategy:<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054128\/0002~~CwmJL0otNjAEAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"110\" \/><\/p>\r\n<p>Pol\u00e1k, P.; Tobrman, T. Dearomatization Strategy for the Synthesis of Arylated 2<em>H<\/em>-Pyrroles and 2,3,5-Trisubstituted 1H-Pyrroles. <br \/><em>Org. Lett.<\/em><strong>\u00a02017<\/strong>,\u00a0<em>19<\/em>, 4608-4611. DOI:\u00a0<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b02219\">10.1021\/acs.orglett.7b02219<\/a><\/p>\r\n<p><br \/><br \/><\/p>\r\n<h2><strong>Cross-coupling reactions of activated C<\/strong><strong>-<\/strong><strong>O bonds for the preparation of tetrasubstituted alkenes<\/strong><\/h2>\r\n<p>The use of activated C-O bonds is an attractive alternative to organohalogen-based electrophilic templates. From a number of ways to activate C-O bonds, we pay attention to reactivity of enol-phosphates. We have recently published a new methodology for the preparation of tamoxifen that uses enol phosphate as a starting compound:<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054128\/0003~~CwmJL0otNjACAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"120\" \/><\/p>\r\n<p>Kotek, V.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T. Aluminium Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues <br \/><em>Eur. J. Org. Chem.<\/em>\u00a0<strong>2016<\/strong>, 5037-5044.\u00a0DOI: <a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201600959\">10.1002\/ejoc.201600959<\/a><\/p>\r\n<p>\u00a0Cross-coupling reactions of activated C-O bonds were also used for the preparation of 2,3-disubstituted-1,3-dienes, [3]- and [4]dendralenes:<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054128\/0004~~CwmJLyhNysnMTkxOVTAyMLSINzQAAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"221\" \/><\/p>\r\n<p>Pol\u00e1k, P.; Tobrman, T. Novel Selective Approach to Terminally Substituted [n]Dendralenes. <br \/><em>Eur. J. Org. Chem.<\/em>\u00a0<strong>2019<\/strong>, 957-968. DOI:<a href=\"https:\/\/doi.org\/10.1002\/ejoc.201801522\">10.1002\/ejoc.201801522<\/a><\/p>\r\n<p>\u00a0<\/p>\r\n<p>We also described the synthesis of biologically active substance starting from enol phosphate:<\/p>\r\n<p><img src=\"\/images\/450!0\/uzel\/0054128\/0005~~CwmJL0otNjAGAA.png\" style=\"display: block; margin-left: auto; margin-right: auto;\" alt=\"\" width=\"450\" height=\"135\" \/><\/p>\r\n<p>Pol\u00e1k, P.; Tobrman, T. The synthesis of polysubstituted indoles from 3-bromo-2-indolyl phosphates <br \/><em>Org. Biomol. Chem.<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>15<\/em>, 6233-6241. DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7OB01127J\">10.1039\/C7OB01127J<\/a><\/p>\r\n<p><\/p>\";s:13:\"urlnadstranka\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["54131"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"54131":{"idvazba":"168046","nad_uzel":"136641","pod_uzel":"54131","url":"","sablona":"4","nazev":"Tobrman's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"27.04.2020 17:21:00","platne_do":null,"iduzel":"54131","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}},"136649":{"idvazba":"168055","nad_uzel":"136640","pod_uzel":"136649","url":"\/research\/tobrman\/publications_clone_96318","sablona":"1","nazev":"Publications","_url_prefix":"{\/\/uoch.vscht.cz\/research\/tobrman\/publications_clone_96318}","poradi":"4","skupina_www":"everyone","platne_od":"12.05.2026 21:35:58.50115","platne_do":null,"iduzel":"136649","obsah":"a:9:{s:5:\"nazev\";s:0:\"\";s:9:\"seo_title\";s:12:\"Publications\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:5:\"obsah\";s:40061:\"<p><strong>2024<\/strong><\/p>\r\n<ul>\r\n<li>P. Oeser and T. Tobrman, Organophosphates as Versatile Substrates in Organic Synthesis. <em>Molecules<\/em> <strong>2024<\/strong>, <em>29<\/em>, 1593. DOI:<a href=\"https:\/\/doi.org\/10.3390\/molecules29071593\">10.3390\/molecules29071593<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>S. Nizi\u0144ski, N. Varma, M. Sikorski, T. Tobrman, E. Svobodov\u00e1, R. Cibulka, M. F. Rode and G. Burdzinski, Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivative. <em>Sci. Rep.<\/em> <strong>2024<\/strong>, <em>14<\/em>, 24375. DOI:<a href=\"https:\/\/doi.org\/10.1038\/s41598-024-75239-x\">10.1038\/s41598-024-75239-x<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>T. Tobrman, 9.14.5 Phospholes (Update 2024),&nbsp; <em>Science of Synthesis<\/em>&nbsp;<strong>2024,<\/strong> <em>1<\/em>, 133. DOI: <a href=\"https:\/\/doi.org\/10.1055\/sos-SD-109-00525\">10.1055\/sos-SD-109-00525<\/a><\/li>\r\n<\/ul>\r\n<p><strong>2023<\/strong><\/p>\r\n<ul>\r\n<li>J. Koudelka, M. Vosmansk\u00e1 and T. Tobrman, Synthesis of Sulfonic Acid Salts and Sulfonic Acids by Advanced Cross-Coupling Reaction of Vinyl Sulfonates. <em>ChemistrySelect<\/em> <strong>2023<\/strong>, <em>8<\/em>, e202304246. DOI:<a href=\"https:\/\/doi.org\/10.1002\/slct.202304246\">10.1002\/slct.202304246<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>T. Tobrman, Vinyl Esters and Vinyl Sulfonates as Green Alternatives to Vinyl Bromide for the Synthesis of Monosubstituted Alkenes via Transition-Metal-Catalyzed Reactions. <em>Chemistry<\/em> <strong>2023<\/strong>, <em>5<\/em>, 2288\u20132321. DOI:<a href=\"https:\/\/www.mdpi.com\/2624-8549\/5\/4\/153\">10.3390\/chemistry5040153<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>L. Kol\u00e1\u010dn\u00e1, P. Pol\u00e1k, A. Li\u0161ka, T. Tobrman and J. Ludv\u00edk, Pentasubstituted Phospholes with extended \u03c0-conjugated Arm \u2013 Synthesis, electrochemistry, spectra and quantum chemical calculations.&nbsp;<em>Electrochim. Acta<\/em> <strong>2023,<\/strong> <em>468,<\/em> 143073. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2023.143073\">10.1016\/j.electacta.2023.143073<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>M. \u010cubi\u0148\u00e1k, N. Varma, P. Oeser, A. Pokluda, T. Pavlovska, R. Cibulka, M. Sikorski, T. Tobrman, Tuning the Photophysical Properties of Flavins by Attaching an Aryl Moiety via Direct C\u2013C Bond Coupling. <em>J. Org. Chem.<\/em> <strong>2023,<\/strong> <em>88, <\/em>218\u2013229. DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.2c02168\">10.1021\/acs.joc.2c02168<\/a><\/li>\r\n<\/ul>\r\n<p><strong>2022<\/strong><\/p>\r\n<ul>\r\n<li>Tobrman, T.; Mrkobrada, S., Palladium-Catalyzed Cross-Coupling Reactions of Borylated Alkenes for the Stereoselective Synthesis of Tetrasubstituted Double Bond. <em>Organics<\/em> <strong>2022<\/strong>, <em>3<\/em>, 210.<a href=\"https:\/\/www.mdpi.com\/2673-401X\/3\/3\/17\" rel=\"follow\">10.3390\/org3030017<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>Shishkanova, T. V.; Tobrman, T.; Otta, J.; Broncov\u00e1, G.; Fitl, P.; Vr\u0148ata, M., Substituted polythiophene-based sensor for detection of ammonia in gaseous and aqueous environment. <em>J. Mater. Sci.<\/em> <strong>2022<\/strong>, <em>57,<\/em> 17870<span _ngcontent-c15=\"\">\u2013<\/span>17882. DOI: <a href=\"https:\/\/link.springer.com\/article\/10.1007\/s10853-022-07694-8\" rel=\"follow\">10.1007\/s10853-022-07694-8<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<ul>\r\n<li>Oeser, P.;&nbsp; Petrenko, A.; Edlov\u00e1, T.; \u010cubi\u0148\u00e1k, M.; Koudelka, J.; Tobrman, T., Halocyclobutanol Dehydration En Route to Halocyclobutenes. <em>Synthesis<\/em> <strong>2022,<\/strong> <em>54,<\/em> 3239<span _ngcontent-c15=\"\">\u20133248. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-1794-0685\" rel=\"follow\">10.1055\/a-1794-0685<\/a><\/span><\/li>\r\n<\/ul>\r\n<p><span _ngcontent-c15=\"\"><\/span><\/p>\r\n<ul>\r\n<li>Kol\u00e1\u010dn\u00e1, L.; Kl\u00edma, J.; Pol\u00e1k, P.; Tobrman, T.; Li\u0161ka, A.; Ludv\u00edk, J., Electrochemical, EPR, and computational study of pyrene conjugates<span _ngcontent-c15=\"\">\u2013<\/span>precursors for novel type of organic semiconductors. <em>J. Solid State Electrochem.<\/em> <strong>2022<\/strong>, <em>26<\/em>, 503<span _ngcontent-c15=\"\">\u2013<\/span>514. DOI: <a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs10008-021-05094-7\" target=\"_blank\" rel=\"follow noopener\">10.1007\/s10008-021-05094-7<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<p><strong>2021<\/strong><\/p>\r\n<ul>\r\n<li>Oeser, P; Koudelka, J.; Petrenko, A.; T. Tobrman, Recent Progress Concerning the <i>N<\/i>-Arylation of Indoles. <i>Molecules <\/i><b>2021<\/b>, <i>26<\/i>, 5079. DOI: <a href=\"https:\/\/www.mdpi.com\/1420-3049\/26\/16\/5079\" target=\"_blank\" rel=\"follow noopener\">10.3390\/molecules26165079<\/a>&nbsp;&nbsp;<\/li>\r\n<\/ul>\r\n<ul>\r\n<li>\u010cubi\u0148\u00e1k, M.; Bigeon, J.; Gal\u00e1\u0159, P.; Ondi\u010d, L.; Tobrman, T., The Synthesis of Tetrasubstituted Cycloalkenes Bearing \u03c0-Conjugated Substituents and Their Optical Properties. <i>ChemistrySelect<\/i> <b>2021<\/b>, <i>6<\/i>, 9904<span _ngcontent-c15=\"\">\u2013<\/span>9910. DOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/slct.202103122\" target=\"_blank\" rel=\"follow noopener\">10.1002\/slct.202103122<\/a><\/li>\r\n<\/ul>\r\n<ul>\r\n<li>Oeser, P.; Edlov\u00e1, T.; \u010cubi\u0148\u00e1k, M.; Tobrman, T., Transition-Metal-Free Ring-Opening Reaction of 2-Halocyclobutanols through Ring Contraction. <i>Eur<\/i><i>. <\/i><i>J<\/i><i>. <\/i><i>Org<\/i><i>. <\/i><i>Chem<\/i><i>.<\/i> <b>2021<\/b>, 4958<span _ngcontent-c15=\"\">\u2013<\/span>4967. DOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.202100837\" target=\"_blank\" rel=\"follow noopener\">10.1002\/ejoc.202100837<\/a><\/li>\r\n<\/ul>\r\n<ul>\r\n<li><span class=\"authors ng-star-inserted\">Koudelka, J.;<\/span> Tobrman, T., Synthesis of 2-Substituted Cyclobutanones by a Suzuki Reaction and Dephosphorylation Sequence. <em>Eur. J. Org. Chem.<\/em> <strong>2021<\/strong>, <span _ngcontent-c15=\"\">3260\u20133269 DOI:<a href=\"https:\/\/doi.org\/10.1002\/ejoc.202100464\" target=\"_blank\" class=\"doi-link\" rel=\"follow noopener\">10.1002\/ejoc.202100464<\/a><br><br><\/span><\/li>\r\n<li><span class=\"authors ng-star-inserted\">Edlov\u00e1, T.; Dvo\u0159\u00e1kov\u00e1, H.; Eigner, V.; <\/span>Tobrman, T., Substrate-Controlled Regioselective Bromination of 1,2-Disubstituted Cyclobutenes: An Application in the Synthesis of 2,3-Disubstituted Cyclobutenones.<br><em>J. Org. Chem.<\/em><strong> 2021<\/strong>,<em> 86<\/em>, <span _ngcontent-c15=\"\">5820\u20135831 DOI:<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.1c00261\" target=\"_blank\" class=\"doi-link\" rel=\"follow noopener\">10.1021\/acs.joc.1c00261<\/a><br><\/span><br><span class=\"authors ng-star-inserted\"><\/span><\/li>\r\n<li><span class=\"authors ng-star-inserted\">Shishkanova, T.; Step\u00e1nkov\u00e1, N.; Tlust\u00fd, M.<\/span>; Tobrman, T.; J<span class=\"authors ng-star-inserted\">ur\u00e1sek, B.; Kucha\u0159, M.; Trchov\u00e1, M.; Fitl, P.; Vr\u0148ata, M., Electrochemically oxidized 15-crown-5 substituted thiophene and host-guest interaction with new psychoactive substances <em>Electrochim. Acta<\/em><strong> 2021<\/strong>,<em>&nbsp;737<\/em>, <span _ngcontent-c15=\"\">137862 DOI:<a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2021.137862\" target=\"_blank\" class=\"doi-link\" rel=\"follow noopener\">10.1016\/j.electacta.2021.137862<\/a><br><\/span><br><\/span><\/li>\r\n<li>Edlov\u00e1, T.; \u010cubi\u0148\u00e1k, M.; Tobrman, T., Cross-Coupling Reactions of Double or Triple Electrophilic Templates for Alkene Synthesis. <i>Synthesis<\/i> <b>2021<\/b>, <i>53<\/i>, 255<span _ngcontent-c15=\"\">\u2013<\/span>266. DOI: <a href=\"https:\/\/doi.org\/10.1055\/s-0040-1707270\" target=\"_blank\" rel=\"follow noopener\">10.1055\/s-0040-1707270<\/a><\/li>\r\n<\/ul>\r\n<p><strong><\/strong><\/p>\r\n<p><strong>2020<\/strong><\/p>\r\n<ul>\r\n<li>Oeser, P.; Koudelka, J.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T., Formation of trisubstituted buta-1,3-dienes and \u03b1,\u03b2-unsaturated ketones via the reaction of functionalized vinyl phosphates and vinyl phosphordiamidates with organometallic reagents. <i>RSC <\/i><i>Adv<\/i><i>.<\/i> <b>2020<\/b>, <i>10<\/i>, 35109<span _ngcontent-c15=\"\">\u2013<\/span>35120. DOI: <a href=\"https:\/\/doi.org\/10.1039\/D0RA07472A\" target=\"_blank\" rel=\"follow noopener\">10.1039\/D0RA07472A<\/a><br><br><\/li>\r\n<li>\u010cubi\u0148\u00e1k, M.; Tobrman, T., Room-Temperature Negishi Reaction of Trisubstituted Vinyl Phosphates for the Synthesis of Tetrasubstituted Alkenes. <i>J. Org<\/i><i>. <\/i><i>Chem<\/i><i>.<\/i> <b>2020<\/b>, <i>85<\/i>, 10728<span _ngcontent-c15=\"\">\u2013<\/span>10739. DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.joc.0c01254\" target=\"_blank\" rel=\"follow noopener\">10.1021\/acs.joc.0c01254<\/a><br><br><\/li>\r\n<li>Pol\u00e1k, P.; \u010cejka, J.; Tobrman, T., Formal Transition-Metal-Catalyzed Phosphole C\u2013H Activation for the Synthesis of Pentasubstituted Phospholes. <em style=\"font-weight: inherit;\">Org. Lett. <\/em><strong style=\"font-size: 15px;\">2020<\/strong><span style=\"color: #333333; font-size: 15px;\">, <\/span><em style=\"font-weight: inherit;\">22<\/em><span style=\"color: #333333; font-size: 15px;\">, 2187<span _ngcontent-c15=\"\">\u2013<\/span>2190. DOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.0c00359\" target=\"_blank\" rel=\"follow noopener\">10.1021\/acs.orglett.0c00359<\/a><br><br><\/span><\/li>\r\n<li><span style=\"color: #333333; font-size: 15px;\">Tobrman, T; Krupi\u010dka, M.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; \u010cubi\u0148\u00e1k, M.; Babor, M.; Dvo\u0159\u00e1k, D., <\/span>Diastereoselective Cyclopropanation through Michael Addition\u2010Initiated Ring Closure between \u03b1,\u03b1\u2010Dibromoketones and \u03b1,\u03b2\u2010Unsaturated Fischer Carbene Complexes. <em style=\"font-weight: inherit;\">Eur. J. Org. Chem.<\/em> <strong style=\"font-size: 15px;\">2020<\/strong><span style=\"color: #333333; font-size: 15px;\">, 429<span _ngcontent-c15=\"\">\u2013<\/span>436. DOI: <a href=\"http:\/\/dx.doi.org\/10.1016\/ejoc.201901503\" target=\"_blank\" rel=\"follow noopener\">10.1002\/ejoc.201901503<\/a><br><br><\/span><\/li>\r\n<li>Guricov\u00e1, M.; Tobrman, T; Pi\u017el, M.; \u017di\u017ekov\u00e1, S.; Hoskovcov\u00e1, I.; Dvo\u0159\u00e1k, D., Synthesis, characterisation and electrochemical properties of Cr(0) aminocarbene complexes containing condensed heteroaromatic moiety. <em>J. Organomet. Chem.<\/em> <strong>2020<\/strong>, <em>905<\/em>, 121023 DOI: <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jorganchem.2019.121023\" target=\"_blank\" rel=\"follow noopener\">10.1016\/j.jorganchem.2019.121023<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<p><strong>2019<\/strong><\/p>\r\n<ul>\r\n<li>Tobrman, T.; \u010cubi\u0148\u00e1k, M.; Dvo\u0159\u00e1k, D., Stereoselective synthesis of trisubstituted alkenyl Fischer aminocarbenes through self-mediated \u03b1-haloketone olefination. <em style=\"font-weight: inherit;\">J. Organomet. Chem.<\/em> <strong style=\"font-size: 15px;\">2019<\/strong><span style=\"color: #333333; font-size: 15px;\">, 902, 120971. DOI: <a href=\"http:\/\/dx.doi.org\/10.1016\/j.jorganchem.2019.120971\" target=\"_blank\" rel=\"follow noopener\">10.1016\/j.jorganchem.2019.120971<\/a><br><br><\/span><\/li>\r\n<li>\u010cubi\u0148\u00e1k, M.; Edlov\u00e1, T.; Pol\u00e1k, P.; Tobrman, T., Indolylboronic Acids: Preparation and Applications.<br><em>Molecules<\/em> <strong>2019<\/strong>, 24, 3523 DOI: <a href=\"https:\/\/doi.org\/10.3390\/molecules24193523\" target=\"_blank\" rel=\"follow noopener\">10.3390\/molecules24193523<\/a><br><br><\/li>\r\n<li>V\u00e1\u0148ov\u00e1, H.; Tobrman, T.; Babor, M.; Dvo\u0159\u00e1k, D., Reaction of lithiated thiophene-derived aminocarbene complexes with inorganic halides: Preparation of a heteroatom containing mono- and multicarbene complexes. <em>J. Organomet. Chem.<\/em> <strong>2019<\/strong>, 882, 90<span _ngcontent-c15=\"\">\u2013<\/span>95 DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2018.12.015\" target=\"_blank\" rel=\"follow noopener\">10.1016\/j.jorganchem.2018.12.015<\/a><br><br><\/li>\r\n<li>Tobrman, T.; Pol\u00e1k, P.; \u010cubi\u0148\u00e1k, M.; Dvo\u0159\u00e1kov\u00e1, H.; Dvo\u0159\u00e1k, D., Dichotomy within 1,4-addition of organolithium and Grignard reagents to \u03b1,\u03b2-unsaturated Fischer alkoxycarbenes: A new synthesis of Fischer carbenes. <em>Tetrahedron<\/em> <strong>2019<\/strong>, <em>75<\/em>, 2175<span _ngcontent-c15=\"\">\u2013<\/span>2181 DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.tet.2019.02.038\" target=\"_blank\" rel=\"follow noopener\">10.1016\/j.tet.2019.02.038<\/a><br><br><\/li>\r\n<li>Pol\u00e1k, P.; Tobrman, T., Novel Selective Approach to Terminally Substituted [n]Dendralenes<br><em>Eur. J. Org. Chem.<\/em> <strong>2019<\/strong>, 957<span _ngcontent-c15=\"\">\u2013<\/span>968. DOI:<a href=\"https:\/\/doi.org\/10.1002\/ejoc.201801522\" target=\"_blank\" rel=\"follow noopener\">10.1002\/ejoc.201801522<\/a><br><br><\/li>\r\n<\/ul>\r\n<p><strong>2018<\/strong><\/p>\r\n<ul>\r\n<li>\u010cubi\u0148\u00e1k, M.; Eigner, V.; Tobrman, T., Bench-Stable Sulfoxide-Based Boronates: Preparation and Application in a Tandem Suzuki Reaction. <em>Adv. Synth. Catal.<\/em> <strong>2018<\/strong>, <em>360<\/em>, 4604<span _ngcontent-c15=\"\">\u2013<\/span>4614 DOI: <a href=\"https:\/\/doi.org\/10.1002\/adsc.201801000\" target=\"_blank\" rel=\"follow noopener\">10.1002\/adsc.201801000<\/a><br><br><\/li>\r\n<\/ul>\r\n<p><strong>2017<\/strong><\/p>\r\n<ul>\r\n<li><span class=\"\">Polak, P.; Dvorak, D.; Tobrman, T., <\/span>Cyanogen: A Versatile Reagent for Diversity-\u200bOriented Synthesis<br><em>Synthesis<\/em> <strong>2017<\/strong>, <em>49<\/em>, 1757<span _ngcontent-c15=\"\">\u2013<\/span>1766 DOI:<a href=\"http:\/\/dx.doi.org\/10.1055\/s-0036-1588410\" target=\"_blank\" rel=\"follow noopener\">10.1055\/s-0036-1588410<\/a><br><br><\/li>\r\n<li><span class=\"modra0\"><span class=\"cerna0\">Polak, P.; Tobrman, T.<span class=\"\">, <\/span><\/span><\/span>The synthesis of polysubstituted indoles from 3-\u200bbromo-\u200b2-\u200bindolyl phosphates. <em>Org. Biomol. Chem.<\/em> <strong>2017<\/strong>, <em>15<\/em>, 6233<span _ngcontent-c15=\"\">\u2013<\/span>6241 DOI:<a href=\"http:\/\/dx.doi.org\/10.1039\/C7OB01127J\" target=\"_blank\" rel=\"follow noopener\">10.1039\/C7OB01127J<\/a><br><br><\/li>\r\n<li><span class=\"modra0\"><span class=\"cerna0\">Polak, P.; Tobrman, T.<span class=\"\">, <\/span><\/span><\/span>Dearomatization Strategy for the Synthesis of Arylated 2H-\u200bPyrroles and 2,\u200b3,\u200b5-\u200bTrisubstituted 1H-\u200bPyrroles. <em>Org. Lett.<\/em><strong> 2017<\/strong>, <em>19<\/em>, 460<span _ngcontent-c15=\"\">\u2013<\/span>4611 DOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b02219\" target=\"_blank\" rel=\"follow noopener\">10.1021\/acs.orglett.7b02219<\/a><br><br><\/li>\r\n<li><span class=\"cerna0\"><span class=\"\">\u0160im\u016fnkov\u00e1, N.; Tobrman, T.;<\/span> Eigner, V.; <span class=\"\">Dvo\u0159\u00e1k, D<\/span>.<span class=\"\">, <\/span><\/span>A Study on the Intramolecular Mitsunobu Reaction of N6-(\u03c9-hydroxyalkyl)adenines. <em>J. Heterocyclic Chem<\/em> <strong>2017<\/strong>, asap DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/jhet.2982\" target=\"_blank\" rel=\"follow noopener\">&nbsp;10.1002\/jhet.2982<\/a><\/li>\r\n<\/ul>\r\n<div>\r\n<p><\/p>\r\n<\/div>\r\n<p><\/p>\r\n<p><strong>2016<\/strong><\/p>\r\n<ul>\r\n<li>V\u00e1\u0148ov\u00e1, H.; Tobrman, T.; Hoskovcova, I.; Dvo\u0159\u00e1k, D.<span class=\"\">, <\/span>Modular synthesis of Fischer biscarbene complexes of chromium. <em>Organometallics<\/em> <strong>2016<\/strong>, <em>35<\/em>, 2999<span _ngcontent-c15=\"\">\u2013<\/span>3006. DOI:<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.organomet.6b00527\" target=\"_blank\" rel=\"follow noopener\">10.1021\/acs.organomet.6b00527<\/a><br><br><\/li>\r\n<li>Kotek, V.; Pol\u00e1k, P.; Dvo\u0159\u00e1kov\u00e1, H.; Tobrman, T.<span class=\"\">, <\/span>Aluminium Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues. <em>Eur. J. Org. Chem.<\/em> <strong>2016<\/strong>, 5037<span _ngcontent-c15=\"\">\u2013<\/span>5044. DOI:<a href=\"http:\/\/dx.doi.org\/10.1002\/ejoc.201600959\" target=\"_blank\" rel=\"follow noopener\">10.1002\/ejoc.201600959<\/a><br><br><\/li>\r\n<li>Pol\u00e1k, P.; V\u00e1\u0148ov\u00e1, H.; Dvo\u0159\u00e1k, D.; Tobrman, T.<span class=\"\">, <\/span>Recent Progress in Transition Metal-Catalyzed Stereoselective Synthesis of Acyclic All-Carbon Tetrasubstituted Alkenes. <em>Tetrahedron Lett.<\/em> <strong>2016<\/strong>, <em>57<\/em>, 3684<span _ngcontent-c15=\"\">\u2013<\/span>3693. DOI:<a href=\"http:\/\/dx.doi.org\/10.1016\/j.tetlet.2016.07.030\" target=\"_blank\" id=\"ddDoi\" class=\"S_C_ddDoi\" rel=\"follow noopener\">10.1016\/j.tetlet.2016.07.030<\/a>&nbsp;<br><br><\/li>\r\n<li><span class=\"cerna0\"><span class=\"\">Kote<\/span><span class=\"\">k, V.;<\/span><span class=\"\">&nbsp;Pol\u00e1k, P.;&nbsp;T<\/span><span class=\"\">obrman, T., <\/span>Efficient and Simple Preparation of Functionalized 1,1-Dibromoenol Phosphates.<\/span> <em><span class=\"biblioTitle\">Monat. Chem.<\/span><\/em>&nbsp;<strong>2016<\/strong>, <em>147<\/em>, 405<span _ngcontent-c15=\"\">\u2013<\/span>412. DOI:<a href=\"http:\/\/dx.doi.org\/10.1007\/s00706-015-1613-6\" target=\"_blank\" rel=\"follow noopener\">10.1007\/s00706-015-1613-6<\/a><\/li>\r\n<\/ul>\r\n<p><\/p>\r\n<p><strong><br>2015<\/strong><\/p>\r\n<ul>\r\n<li>Kotek V., Dvo\u0159\u00e1kov\u00e1 H., Tobrman T.<span class=\"\">,<\/span> Modular and highly stereoselective approach to all-carbon tetrasubstituted alkenes. <em>Org. Lett.<\/em>, <strong>2015<\/strong>, <em>17<\/em>, 608<span _ngcontent-c15=\"\">\u2013<\/span>611. DOI: <a href=\"https:\/\/doi.org\/10.1021\/ol503624v\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/ol503624v<\/a><\/li>\r\n<li>K\u0159ov\u00e1\u010dek M., Dvo\u0159\u00e1k D.: Synthesis of potentially biologically active 6-(1,3-butadiynyl)purines. <em>J. Heterocyclic Chem.<\/em>, <strong>2015<\/strong>, <em>52<\/em>, 40<span _ngcontent-c15=\"\">\u2013<\/span>47. DOI: <a href=\"https:\/\/doi.org\/10.1002\/jhet.1938\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/jhet.1938<\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2014<\/strong><\/p>\r\n<ul>\r\n<li>Tobrman T., Jur\u00e1skov\u00e1 I., Dvo\u0159\u00e1k D.<span class=\"\">,<\/span> Negishi cross-coupling reaction as a simple and efficient route to functionalized amino and alkoxy carbene complexes of chromium, molybdenum, and tungsten. <em>Organometallics<\/em>, <strong>2014<\/strong>, <em>33<\/em>, 6593<span _ngcontent-c15=\"\">\u2013<\/span>6603. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om500925m\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om500925m<\/a><\/li>\r\n<li>Kvapilov\u00e1 H., Eigner V., Hoskovcov\u00e1 I., Tobrman T., \u010cejka J., Z\u00e1li\u0161 S., Structural flexibility of 2-hetaryl chromium aminocarbene complexes: Experimental and theoretical evidence. <em>Inorg. Chim. Acta<\/em>, <strong>2014<\/strong>, <em>421<\/em>, 439<span _ngcontent-c15=\"\">\u2013<\/span>445. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.ica.2014.06.028\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.ica.2014.06.028<\/a><\/li>\r\n<li>Vrzal L., Fl\u00eddrov\u00e1 K., Tobrman T, Dvo\u0159\u00e1kov\u00e1 H., Lhot\u00e1k, P., Use of residual dipolar couplings in conformational analysis of meta-disubstituted calix[4]arenes. <em>Chem. Commun.<\/em>, <strong>2014<\/strong>, <em>50<\/em>, 7590<span _ngcontent-c15=\"\">\u2013<\/span>7592. DOI: <a href=\"https:\/\/doi.org\/10.1039\/C4CC02274B\" target=\"_blank\" class=\"text--small\" title=\"Link to landing page via DOI\" rel=\"follow noopener\">10.1039\/C4CC02274B<\/a><\/li>\r\n<li>Tobrman T, Jur\u00e1skov\u00e1 I., V\u00e1\u0148ov\u00e1 H., Dvo\u0159\u00e1k D, Lithiation of chromium and tungsten aminocarbene complexes: An easy approach to functionalized aminocarbene complexes. <em>Organometallics<\/em>, <strong>2014<\/strong>, <em>33<\/em>, 2990<span _ngcontent-c15=\"\">\u2013<\/span>2996. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om500182p\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om500182p<\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., Regioselective and facile synthesis of 7,9-dialkyl-8-oxopurines from 7,9-dialkyl-7,8-dihydropurines: Total synthesis of Heteromines I and J. <em>Synthesis<\/em>, <strong>2014<\/strong>, <em>46<\/em>, 660<span _ngcontent-c15=\"\">\u2013<\/span>668. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0033-1340499\" target=\"_blank\" rel=\"follow noopener\"><span>10.1055\/s-0033-1340499<\/span><\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2013<\/strong><\/p>\r\n<ul>\r\n<li>Mary\u0161ka M., Chud\u00edkov\u00e1 N., Kotek V., Dvo\u0159\u00e1k D., Tobrman T., Regioselective and efficient synthesis of <em>N<\/em><sup>7<\/sup>-substituted adenines, guanines, and 6-mercaptopurines. <em>Monatsh. Chem<\/em>. <strong>2013<\/strong>, <em>144<\/em>, 501<span _ngcontent-c15=\"\">\u2013<\/span>507. DOI: <a href=\"https:\/\/link.springer.com\/article\/10.1007%2Fs00706-012-0899-x#citeas\" target=\"_blank\" rel=\"follow noopener\"><span>10.1007\/s00706-012-0899-x<\/span><\/a><\/li>\r\n<li>Koukal P., Dvo\u0159\u00e1kov\u00e1 H., Dvo\u0159\u00e1k D., Tobrman T., Palladium-Catalyzed Claisen Rearrangement of Allyloxypurines. <em>Chem. Pap.<\/em>, <strong>2013<\/strong>, <em>67<\/em>, 3<span _ngcontent-c15=\"\">\u2013<\/span>8. DOI: <a href=\"https:\/\/link.springer.com\/article\/10.2478%2Fs11696-012-0239-y#citeas\" target=\"_blank\" rel=\"follow noopener\"><span>10.2478\/s11696-012-0239-y<\/span><\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2012<\/strong><\/p>\r\n<ul>\r\n<li>Metelkov\u00e1 R., Tobrman T., Kvapilov\u00e1 H., Hoskovcov\u00e1 I., Ludv\u00edk J., Synthesis, characterization and electrochemical investigation of hetaryl chromium(0) aminocarbene complexes. <em>Electrochim. Acta<\/em>, <strong>2012<\/strong>, <em>82<\/em>, 470<span _ngcontent-c15=\"\">\u2013<\/span>477. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2012.05.027\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.electacta.2012.05.027<\/a><\/li>\r\n<li>Kotek V., Tobrman T., Dvo\u0159\u00e1k D., Highly Efficient and Broad-Scope Protocol for the Preparation of 7-Substituted 6-halopurines via N9-Boc-Protected 7,8-dihydropurines. <em>Synthesis<\/em> <strong>2012<\/strong>, 44, 610<span _ngcontent-c15=\"\">\u2013<\/span>618. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0031-1290068\" target=\"_blank\" rel=\"follow noopener\"><span>10.1055\/s-0031-1290068<\/span><\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2011<\/strong><\/p>\r\n<ul>\r\n<li>Hoskovcov\u00e1 I., Zv\u011b\u0159inov\u00e1 R., Roh\u00e1\u010dov\u00e1 J., Dvo\u0159\u00e1k D., Tobrman T., Z\u00e1li\u0161 S., Ludv\u00edk J, Fischer aminocarbene complexes of chromium and iron: Anomalous electrochemical reduction of p-carbonyl substituted derivatives. <em>Electrochim. Acta<\/em> <strong>2011<\/strong>, <em>56<\/em>, 6853<span _ngcontent-c15=\"\">\u2013<\/span>6859. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2011.05.096\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.electacta.2011.05.096<\/a><\/li>\r\n<li>Tobrmanov\u00e1 M., Tobrman T., Dvo\u0159\u00e1k D., Pd-Catalyzed Allylic Substitution of Purin-8-yl(allyl) Acetate: Route to (E)-Alkenylpurines. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2011<\/strong>, <em>76<\/em>, 311<span _ngcontent-c15=\"\">\u2013<\/span>326. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/76\/4\/0311\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc2011030<\/span><\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2010<\/strong><\/p>\r\n<ul>\r\n<li>Negishi E.-i., Tobrman T., Rao H., Xu S., Lee Ch.-T., Highly (98 %) Selective Alkene Synthesis of Wide Applicability via Fluride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes. <em>Isr. J. Chem.<\/em> <strong>2010<\/strong>, <em>50<\/em>, 696<span _ngcontent-c15=\"\">\u2013<\/span>701. DOI: <a href=\"https:\/\/doi.org\/10.1002\/ijch.201000051\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/ijch.201000051<\/a><\/li>\r\n<li>Kotek V., Chud\u00edkov\u00e1 N., Tobrman T., Dvo\u0159\u00e1k D., Selective Synthesis of 7-substituted Purines via 7,8-dihydropurines. <em>Org. Lett.<\/em> <strong>2010<\/strong>, <em>12<\/em>, 5724<span _ngcontent-c15=\"\">\u2013<\/span>5727. DOI: <a href=\"https:\/\/doi.org\/10.1021\/ol1025525\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/ol1025525<\/a><\/li>\r\n<li>Pa\u0159\u00edk P., Kulh\u00e1nek J., Ludwig M., Wagner R., Rotrekl I., Draho\u0148ovsk\u00fd D., Meca L., \u0160m\u00eddkov\u00e1 M., Tobrman T., Dvo\u0159\u00e1k D., Acidity of Benzoic Acids Bearing the (CO)<sub>5<\/sub>Cr=CN(CH<sub>3<\/sub>)<sub>2<\/sub> Group. <em>Organometallics<\/em> <strong>2010<\/strong>, <em>29<\/em>, 4135<span _ngcontent-c15=\"\">\u2013<\/span>4138. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om100608x\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om100608x<\/a><\/li>\r\n<li>Hoskovcov\u00e1 I., Roh\u00e1\u010dov\u00e1 J., Dvo\u0159\u00e1k D., Tobrman T., Z\u00e1li\u0161 S., Zv\u011b\u0159inov\u00e1 R., Ludv\u00edk J., Synthesis and electrochemical study of iron, chromium and tungsten aminocarbenes: Role of ligand structure and central metal nature. <em>Electrochim. Acta<\/em>, <strong>2010<\/strong>, <em>55<\/em>, 8341<span _ngcontent-c15=\"\">\u2013<\/span>8351. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2010.02.057\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.electacta.2010.02.057<\/a><\/li>\r\n<li>Kle\u010dka M., K\u0159ov\u00e1\u010dek M., Tobrman T., Dvo\u0159\u00e1k D., Synthesis of (<em>E<\/em>)-6-Alkenylpurines via Pd-Catalyzed Stannation\/Protodestannation Tandem Process of Alkynylpurines. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2010<\/strong>, <em>75<\/em>, 313<span _ngcontent-c15=\"\">\u2013<\/span>332. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/75\/3\/0313\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc2009563<\/span><\/a><\/li>\r\n<li>Wang C., Xu Z., Tobrman T., Negishi E.-i., Arylethyne Bromoboration-Negishi Coupling Route to <em>E<\/em>- or <em>Z<\/em>-Aryl-Substituted Trisubstituted Alkenes of &gt;98% Isomeric Purity. New Horizon in the Highly Selective Synthesis of Trisubstituted Alkenes. <em>Adv. Synth Catal.<\/em>, <strong>2010<\/strong>, <em>352<\/em>, 627<span _ngcontent-c15=\"\">\u2013<\/span>631. DOI: <a href=\"https:\/\/doi.org\/10.1002\/adsc.200900766\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/adsc.200900766<\/a><\/li>\r\n<\/ul>\r\n<p><strong>&nbsp;&nbsp;<\/strong><\/p>\r\n<p><strong><a><\/a>2009-1996<\/strong><\/p>\r\n<ul>\r\n<li>Wang C., Tobrman T., Xu Z., Negishi E.-i., Highly Regio- and Stereoselective Synthesis of (<em>Z<\/em>)-Trisubstituted Alkenes via Propyne Bromoboration and Tandem Pd-Catalyzed Cross-Coupling. <em>Org. Lett.<\/em> <strong>2009<\/strong>, <em>11<\/em>, 4092<span _ngcontent-c15=\"\">\u2013<\/span>4095. DOI: <a href=\"https:\/\/doi.org\/10.1021\/ol901566e\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/ol901566e<\/a><\/li>\r\n<li>Keder R., Dvo\u0159\u00e1kov\u00e1 H., Dvo\u0159\u00e1k D., New Approach to the Synthesis of N-7-Arylguanines and N-7-Aryladenines. <em>Eur. J. Org. Chem.<\/em> <strong>2009<\/strong>, 1522<span _ngcontent-c15=\"\">\u2013<\/span>1531. DOI: <a href=\"https:\/\/doi.org\/10.1002\/ejoc.200801002\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/ejoc.200801002<\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., Heck reactions of 6- and 2-halopurines. <em>Eur. J. Org. Chem.<\/em> <strong>2008<\/strong>, 2923\u20132928. DOI: <a href=\"https:\/\/doi.org\/10.1002\/ejoc.200800091\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/ejoc.200800091<\/a><\/li>\r\n<li>Krou\u017eelka J., Linhart I., Tobrman T., Synthesis of 3-(2-hydroxy-1-phenylethyl)- and 3-(2-hydroxy-2-phenylehtyl)adenine, DNA adducts derived from styrene. <em>J. Heterocyclic Chem.<\/em> <strong>2008<\/strong>, <em>45<\/em>, 789\u2013795. DOI: <a href=\"https:\/\/doi.org\/10.1002\/chin.200838155\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/chin.200838155<\/a><\/li>\r\n<li>Tobrman T., \u0160tepni\u010dka P., C\u00edsa\u0159ov\u00e1 I., Dvo\u0159\u00e1k D., Preparation and crystal structures of purine 2,2\u2019-, 6,6\u2019-, and 8,8\u2019-dimers. <em>Eur. J. Org. Chem.<\/em> <strong>2008<\/strong>, 2167\u20132174. DOI: <a href=\"https:\/\/doi.org\/10.1002\/ejoc.200800017\" target=\"_blank\" class=\"epub-doi\" rel=\"follow noopener\" aria-label=\"Digital Object Identifier\">10.1002\/ejoc.200800017<\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., Reductive Dimerization of 2- and 6-Iodopurines: Side reaction in Pd-Catalyzed Cross Coupling of Iodopurines. <em>Collect. Czech Chem. Comm.<\/em> <strong>2007<\/strong>, <em>72<\/em>, 1365<span _ngcontent-c15=\"\">\u2013<\/span>1374. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/72\/10\/1365\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20071365<\/span><\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., Selective magnesiation of chloro-iodopurines: An efficient approach to new purine derivatives. <em>Org. Lett.<\/em> <strong>2006<\/strong>, <em>8<\/em>, 1291<span _ngcontent-c15=\"\">\u2013<\/span>1294. DOI: <a href=\"https:\/\/doi.org\/10.1021\/ol053013w\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/ol053013w<\/a><\/li>\r\n<li>Tobrman T., Meca L., Dvo\u0159\u00e1kov\u00e1 H., \u010cern\u00fd J., Dvo\u0159\u00e1k D., Study of the Origin of the Hindered Rotation of an Aryl Ring in the Chromium Aminocarbene Complexes Bearing Aromatic Ring Atteched to the Carbene Carbon Atom. <em>Organometalics<\/em> <strong>2006<\/strong>, <em>25<\/em>, 5540<span _ngcontent-c15=\"\">\u2013<\/span>5548. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om0605837\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om0605837<\/a><\/li>\r\n<li>Kle\u010dka M., Tobrman T., Dvo\u0159\u00e1k D., Cu(I)-catalyzed coupling of (9-benzylpurin-6-yl)magnesium chloride with allyl halides: an approach to 6-allylpurine derivatives. <em>Collect. Czech Chem. Comm.<\/em> <strong>2006<\/strong>, <em>71<\/em>, 1221<span _ngcontent-c15=\"\">\u2013<\/span>1228. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/71\/8\/1221\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20061221<\/span><\/a><\/li>\r\n<li>Hoskovcov\u00e1 I., Roh\u00e1\u010dov\u00e1 J., Meca L., et al., Electrochemistry of chromium(0)-aminocarbene complexes: The use of intramolecular interaction LFER for characterization of the oxidation and reduction centre of the complex. <em>Electrochim. Acta<\/em> <strong>2005<\/strong>, <em>50<\/em>, 4911<span _ngcontent-c15=\"\">\u2013<\/span>4915. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.electacta.2004.12.047\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.electacta.2004.12.047<\/a><\/li>\r\n<li>Draho\u0148ovsk\u00fd D., \u0160t\u011bpni\u010dka P., Dvo\u0159\u00e1k D., P-chiral 2-{1 '-[butyl(phenyl)phosphanyl]ferrocen-1-yl} -4-isopropyl-4,5-dihydrooxazoles: A second chirality center in catalytic system. <em>Collect. Czech Chem. Comm.<\/em> <strong>2005<\/strong>, <em>70<\/em>, 361<span _ngcontent-c15=\"\">\u2013<\/span>369. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/70\/3\/0361\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20050361<\/span><\/a><\/li>\r\n<li>Meca L., Dvo\u0159\u00e1k D., Ludv\u00edk J., et al., Synthesis, structures, and electrochemistry of group 6 aminocarbenes with a P-chelating 1'-(Diphenylphosphino)ferrocenyl substituent <em>Organometallics<\/em> <strong>2004<\/strong>, <em>23<\/em>, 2541<span _ngcontent-c15=\"\">\u2013<\/span>2551. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om040007f\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om040007f<\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., 'Reductive Heck reaction' of 6-halopurines. <em>Tetrahedron Lett.<\/em> <strong>2004<\/strong>, <em>45<\/em>, 273<span _ngcontent-c15=\"\">\u2013<\/span>276. DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2003.10.181\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.tetlet.2003.10.181<\/a><\/li>\r\n<li>Tobrman T., Dvo\u0159\u00e1k D., 6-Magnesiated purines: Preparation and reaction with aldehydes. <em>Org. Lett.<\/em> <strong>2003<\/strong>, <em>5<\/em>, 4289<span _ngcontent-c15=\"\">\u2013<\/span>4291. DOI: <a href=\"https:\/\/doi.org\/10.1021\/ol0355027\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/ol0355027<\/a><\/li>\r\n<li>Hocek M., Dvo\u0159\u00e1k D., Havelkov\u00e1 M., Covalent analogues of nucleobase-pairs. <em>Nucleoside Nucleotides &amp; Nucleic Acids<\/em> <strong>2003<\/strong>, <em>22<\/em>, 775<span _ngcontent-c15=\"\">\u2013<\/span>777. DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1081\/NCN-120022632\" target=\"_blank\" rel=\"follow noopener\">10.1081\/NCN-120022632<\/a><\/li>\r\n<li>Meca L., C\u00edsa\u0159ov\u00e1 I., Dvo\u0159\u00e1k D., Thermolysis of iron N-allylaminocarbene complexes: Formation of eta(3)-1-azaallylirontricarbonyl complexes. Synthetic and theoretical study. <em>Organometallics<\/em> <strong>2003<\/strong>, <em>22<\/em>, 3703<span _ngcontent-c15=\"\">\u2013<\/span>3709. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om0301280\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om0301280<\/a><\/li>\r\n<li>Draho\u0148ovsk\u00fd D., Borgo V., Dvo\u0159\u00e1k D., Fischer chromium carbene complexes as nucleophiles in palladium-catalyzed allylic substitution reactions. <em>Tetrahedron Lett.<\/em> <strong>2002<\/strong>, <em>43<\/em>, 7867<span _ngcontent-c15=\"\">\u2013<\/span>7869. DOI: <a href=\"https:\/\/doi.org\/10.1016\/S0040-4039(02)01913-5\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/S0040-4039(02)01913-5<\/a><\/li>\r\n<li>Havelkov\u00e1 M., Dvo\u0159\u00e1k D., Hocek M., Covalent analogues of DNA base-pairs and triplets. Part 3: Synthesis of 1 ,4-and 1,3-bis(purin-6-yl)benzenes and 1-(1,3-dimethyluracil-5-yl)-3 or 4-(purin-9-yl)benzenes. <em>Tetrahedron<\/em> <strong>2002<\/strong>, <em>58<\/em>, 7431<span _ngcontent-c15=\"\">\u2013<\/span>7435. DOI: <a href=\"https:\/\/doi.org\/10.1016\/S0040-4020(02)00833-5\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/S0040-4020(02)00833-5<\/a><\/li>\r\n<li>Havr\u00e1nek M., Dvo\u0159\u00e1k D., 3,3-disubstituted allyl alcohols from palladium-catalyzed coupling of hydroaluminated propargyl alcohols with aryl iodides. <em>J. Org. Chem.<\/em> <strong>2002<\/strong>, <em>67<\/em>, 2125<span _ngcontent-c15=\"\">\u2013<\/span>2130. DOI: <a href=\"https:\/\/doi.org\/10.1021\/jo0162235\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/jo0162235<\/a><\/li>\r\n<li>Vyklick\u00fd L., Dvo\u0159\u00e1kov\u00e1 H., Dvo\u0159\u00e1k D., Iron aminocarbene complexes containing a double C=C bond in the N-substituent: Preparation and reactivity. <em>Organometallics<\/em> <strong>2001<\/strong>, <em>20<\/em>, 5419<span _ngcontent-c15=\"\">\u2013<\/span>5424. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om010533w\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om010533w<\/a><\/li>\r\n<li>Havelkov\u00e1 M., Dvo\u0159\u00e1k D., Hocek M., The Suzuki-Miyaura cross-coupling reactions of 2-, 6-or 8-halopurines with boronic acids leading to 2-, 6-or 8-aryl- and -alkenylpurine derivatives. <em>Synthesis<\/em> <strong>2001<\/strong>, 1704<span _ngcontent-c15=\"\">\u2013<\/span>1710. DOI: <a href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-1999-2753\" target=\"_blank\" rel=\"follow noopener\"><span>10.1055\/s-1999-2753<\/span><\/a><\/li>\r\n<li>Draho\u0148ovsk\u00fd D., C\u00edsa\u0159ov\u00e1 I., \u0160t\u011bpni\u010dka P., et al., An alternative approach to chiral 2-[1 '-(diphenylphosphanyl)ferrocenyl]-4,5-dihydrooxazoles. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2001<\/strong>, <em>66<\/em>, 588<span _ngcontent-c15=\"\">\u2013<\/span>604. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/66\/4\/0588\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20010588<\/span><\/a><\/li>\r\n<li>Rotrekl I., Vyklick\u00fd L., Dvo\u0159\u00e1k D., Reaction of iron aminocarbene complexes with electronically deficient alkenes. <em>J. Organometallic Chem.<\/em> <strong>2001<\/strong>, <em>617<\/em>, 329<span _ngcontent-c15=\"\">\u2013<\/span>333. DOI: <a href=\"https:\/\/doi.org\/10.1016\/S0022-328X(00)00707-5\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/S0022-328X(00)00707-5<\/a><\/li>\r\n<li>Havelkov\u00e1 M., Studenovsk\u00fd M., Dvo\u0159\u00e1k D., <em>N<\/em>-1-substituted hypoxanthine derivatives from the reaction of 6-halopurines with Michael acceptors under the conditions of Heck reaction. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 797<span _ngcontent-c15=\"\">\u2013<\/span>804. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/65\/5\/0797\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20000797<\/span><\/a><\/li>\r\n<li>Havr\u00e1nek M., Dvo\u0159\u00e1k D., 3-(tributylstannyl)allyl alcohols: Useful building blocks for solid-phase synthesis of skipped dienes and trienes. <em>Collect. Czech. Chem. Commun.<\/em> <strong>2000<\/strong>, <em>65<\/em>, 434<span _ngcontent-c15=\"\">\u2013<\/span>454. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/65\/3\/0434\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc20000434<\/span><\/a><\/li>\r\n<li>Havelkov\u00e1 M., Hocek M., \u010cesnek M., et al., The Suzuki-Miyaura cross-coupling reactions of 6-halopurines with boronic acids leading to 6-aryl- and 6-alkenylpurines. <em>Synlett<\/em> <strong>1999<\/strong>, 1145<span _ngcontent-c15=\"\">\u2013<\/span>1147. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-1999-2753\" target=\"_blank\" rel=\"follow noopener\"><span>10.1055\/s-1999-2753<\/span><\/a><\/li>\r\n<li>Such\u00fd P., Dvo\u0159\u00e1k D., Havelkov\u00e1 M., Unexpected course of the reaction of 1,3-bis(dimethylamino)trimethinium perchlorate with 3-substituted prop-2-ynals leading to 1-aryl-2,4,6-triformylbenzenes. <em>Collect. Czech. Chem. Commun.<\/em> <strong>1999<\/strong>, <em>64<\/em>, 119<span _ngcontent-c15=\"\">\u2013<\/span>129. DOI: <span>1<a href=\"http:\/\/cccc.uochb.cas.cz\/64\/1\/0119\/\" target=\"_blank\" rel=\"follow noopener\">0.1135\/cccc19990119<\/a><\/span><\/li>\r\n<li>Dvo\u0159\u00e1kov\u00e1 H., Dvo\u0159\u00e1k D., Hol\u00fd A., Synthesis of acyclic nucleotide analogues derived from 6-(sec- or tert-alkyl)purines via coupling of 6-chloropurine derivatives with organocuprates. <em>Collect. Czech. Chem. Commun.<\/em> <strong>1998<\/strong>, <em>63<\/em>, 2065<span _ngcontent-c15=\"\">\u2013<\/span>2074. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/63\/12\/2065\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc19982065<\/span><\/a><\/li>\r\n<li>Havr\u00e1nek M., Dvo\u0159\u00e1k D., Transmetallation from aluminum to tin: A facile preparation of tributylstannylprop-2-en-1-ols. <em>Synthesis<\/em> <strong>1998<\/strong>, 1264<span _ngcontent-c15=\"\">\u2013<\/span>1268. DOI: <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-1998-6101\" target=\"_blank\" rel=\"follow noopener\"><span>10.1055\/s-1998-6101<\/span><\/a><\/li>\r\n<li>Dvo\u0159\u00e1k D., Ludwig M., [(<em>N<\/em>,<em>N<\/em>-dimethylamino)carboxymethylene]pentacarbonyl-chromium(0): The first Fischer carbene complex with a free carboxyl group attached directly to the carbene atom. <em>Organometallics<\/em> <strong>1998<\/strong>, <em>17<\/em>, 3627<span _ngcontent-c15=\"\">\u2013<\/span>3629. DOI: <a href=\"https:\/\/doi.org\/10.1021\/om980082o\" target=\"_blank\" title=\"DOI URL\" rel=\"follow noopener\">10.1021\/om980082o<\/a><\/li>\r\n<li>Dvo\u0159\u00e1k D., <a href=\"http:\/\/www.chemicke-listy.cz\/docs\/full\/1997_04_216-226.pdf\" target=\"_blank\" rel=\"follow noopener\">Transition metals in organic synthesis - Basic principles<\/a>. <em>Chemick\u00e9 Listy<\/em> <strong>1997<\/strong>, <em>91<\/em>, 216<span _ngcontent-c15=\"\">\u2013<\/span>226.<\/li>\r\n<li>Arnold Z., Dvo\u0159\u00e1k D., Havr\u00e1nek M., Convenient preparation of 1,3-bis(dimethylamino)trimethinium perchlorate, tetrafluoroborate and hexafluorophosphate. <em>Collect. Czech. Chem. Commun.<\/em> <strong>1996<\/strong>, <em>61<\/em>, 1637<span _ngcontent-c15=\"\">\u2013<\/span>1641. DOI: <a href=\"http:\/\/cccc.uochb.cas.cz\/61\/11\/1637\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc19961637<\/span><\/a><\/li>\r\n<li>Wagner R., Dvo\u0159\u00e1k D., Hol\u00fd A.: New application of the Stille coupling in the synthesis of 5-substituted uracils. <em>Collect. Czech. Chem. Commun.<\/em> <strong>1996<\/strong>, <em>61<\/em>, S118<span _ngcontent-c15=\"\">\u2013<\/span>S119 Sp. Iss. SI. DOI: <a href=\"http:\/\/pikka.uochb.cas.cz\/61\/special_issue\/0118\/\" target=\"_blank\" rel=\"follow noopener\"><span>10.1135\/cccc1996s118<\/span><\/a><\/li>\r\n<li>Dvo\u0159\u00e1kov\u00e1 H., Dvo\u0159\u00e1k D., Hol\u00fd A., Coupling of 6-chloropurines with organocuprates derived from Grignard reagents: A convenient route to sec and tert 6-alkylpurines. <em>Tetrahedron Lett.<\/em> <strong>1996<\/strong>, <em>37<\/em>, 1285<span _ngcontent-c15=\"\">\u2013<\/span>1288. DOI: <a href=\"https:\/\/doi.org\/10.1016\/0040-4039(95)02375-5\" target=\"_blank\" class=\"doi\" title=\"Persistent link using digital object identifier\" rel=\"follow noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/0040-4039(95)02375-5<\/a><\/li>\r\n<\/ul>\";s:13:\"urlnadstranka\";s:0:\"\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";}","class":"stranka","autonomni":"1","pod_uzly":["54131"],"poduzly_count":1,"poduzly_count_aut":0,"poduzly":{"poduzly_count_aut_sum":0,"54131":{"idvazba":"168046","nad_uzel":"136641","pod_uzel":"54131","url":"","sablona":"4","nazev":"Tobrman's Group","_url_prefix":null,"poradi":"1","skupina_www":"everyone","platne_od":"27.04.2020 17:21:00","platne_do":null,"iduzel":"54131","class":"infobox","autonomni":"0","poduzly_count":0,"poduzly_count_aut":0}}}}}}},"117005":{"idvazba":"144424","nad_uzel":"116983","pod_uzel":"117005","url":"\/contact","sablona":"49","nazev":"Contact","_url_prefix":"{\/\/uoch.vscht.cz\/contact}","poradi":"4","skupina_www":"everyone","platne_od":"08.06.2026 20:40:00","platne_do":null,"iduzel":"117005","obsah":"a:14:{s:5:\"nazev\";s:22:\"Contact \u2013 Department\";s:9:\"seo_title\";s:7:\"Contact\";s:8:\"seo_desc\";s:0:\"\";s:5:\"autor\";s:0:\"\";s:11:\"autor_email\";s:0:\"\";s:8:\"autor_no\";s:1:\"1\";s:5:\"perex\";s:0:\"\";s:5:\"ikona\";s:0:\"\";s:7:\"obrazek\";s:0:\"\";s:5:\"vyska\";s:2:\"md\";s:9:\"ogobrazek\";s:0:\"\";s:6:\"pozadi\";s:0:\"\";s:5:\"obsah\";s:713:\"<h2>Address<\/h2>\r\n<p>Department of Organic Chemistry<br>UCT Prague - Faculty of Chemical Technology<br>Technick\u00e1 5<br>166 28 Praha 6 - Dejvice<br>Czech Republic<\/p>\r\n<p>&nbsp;<\/p>\r\n<hr>\r\n<h2>Department's office<\/h2>\r\n<p><a href=\"https:\/\/emil.vscht.cz\/maps\/30482\">A278<\/a><\/p>\r\n<p><\/p>\r\n<p><strong>Head of Department<\/strong>: Prof. Ing. Radek Cibulka, PhD.<\/p>\r\n<p><strong>Secretary of Department:<\/strong> Ing. Mark\u00e9ta Ryb\u00e1\u010dkov\u00e1, Ph.D.<\/p>\r\n<p><strong>Administrative Support&nbsp;of Department:<\/strong> Veronika P\u00edpalov\u00e1<\/p>\r\n<p><strong>Economist of Department: <\/strong>Ing. 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