Publikace

2019

• Jing, H.; Xu, M.; Xiang, Y.; Wang, E.; Liu, D.; Poryvai, A.; Kohout, M.; Éber, N.; Buka, A.:
  Light tunable gratings based on flexoelectric effect in photoresponsive bent-core nematics.
  Adv. Opt. Mater. 2019, 1801790 DOI: 10.1002/adom.201801790
  
  
• Pokluda, A.; Kohout, M.; Chudoba, J.; Krupička, M.; Cibulka, R.:
  Nitrosobenzene: Reagent for the Mitsunobu esterification reaction.
  ACS Omega 2019, 4, 5012-5018 DOI: 10.1021/acsomega.8b03551
  
  
• Spálovská, D.; Maříková, T.; Kohout, M.; Králík, F.; Kuchař, M.; Setnička, V.:
  Methylone and pentylone: Structural analysis of new psychoactive substances.
  Forensic Toxicol. 2019, 37, 366-377 DOI: 10.1007/s11419-019-00468-z
  
  
• 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.
  J. Mol. Liq. 2019, 275, 829-838 DOI: 10.1016/j.molliq.2018.11.058
  
  
• Geibel, C.; Dittrich, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; Lämmerhofer, M.:
  Evaluation of superficially porous particle based zwitterionic chiral ion exchangers against fully porous particle benchmarks for enantioselective ultra-high performance liquid chromatography.
  J. Chromatogr. A 2019, 1603, 130-140 DOI: 10.1016/j.chroma.2019.06.026
  
  
• Poryvai, A.; Vojtylová-Jurkovičová, T.; Šmahel, M.; Kolderová, N.; Tomášková, P.; Sýkora, 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.
  Molecules 2019, 24, 1099 DOI: 10.3390/molecules24061099
  
  
• Tlustý, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhoták, P.:
  Synthesis of upper rim-double-bridged calix[4]arenes bearing seven membered rings and related compounds.
  RSC Adv. 2019, 9, 22017-22030. DOI: 10.1039/C9RA05075B

2018

• Jurásek, B.; Králík, F.; Rimpelová S.; Čejka, J.; Setnička, V.; Ruml, T.; Kuchař, M.; Kohout, M.:
  Synthesis, Absolute Configuration and in vitro Cytotoxicity of Deschloroketamine Enantiomers: Rediscovered and Abused Dissociative Anaesthetic
  New. J. Chem. 2018, 42, 19360-19368 DOI: 10.1039/c8nj03107j
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• 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
  New J. Chem. 2018, 42, 20074-20086 DOI: 10.1039/C8NJ04690E
  
  
• Schmitt, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; Lämmerhofer, M.:
  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
  J. Chromatogr. A 2018, 1569, 149-159 DOI:10.1016/j.chroma.2018.07.056

• Spálovská, D.; Kralik, F.; Kohout, M.; Jurasek, B.; Habartová, L.; Kuchar, M.; Setnicka, V.: 
  Structure determination of butylone as a new psychoactive substance using chiroptical and vibrational spectroscopies 
  Chirality 2018, 30, 548-559 DOI:10.1002/chir.22825
  
  
• Wolrab, D.; Kohout, M.:
  Multimodální stacionární fáze pro kapalinovou chromatografii, způsob jejich přípravy a jejich použití.
  Národní patent č. 307339, číslo přihlášky 2017-193, datum udělení 2.5.2018, datum zveřejnění 13.6.2018.
  
  
• Kohout, M.; Wernisch, S.; Tuma, J.; Hettegger, H.; Picha, J.; Lindner W.: 
  Effect of different immobilization strategies on chiral recognition properties of Cinchona-based anion exchangers 
  J. Sep. Sci. 2018, 41, 1355-1364 DOI:10.1002/jssc.201701213
  
  
• Bajtai, A.; Fekete, B.; Palkó, M.; Fülöp, F.; Lindner, W.; Kohout, M.; Ilisz, I.; Péter, A.: 
  Comparative study on the liquid chromatographic enantioseparation of cyclic β-amino acids and the related cyclic β-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases 
  J. Sep. Sci. 2018, 41, 1216-1223 DOI:10.1002/jssc.201701190
  
  
• Sardella, R.; Macchiarulo, A.; Urbinati, F.; Ianni, F.; Carotti, A.; Kohout, M.; Lindner, W.; Péter, A.; Ilisz, I.: 
  Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers 
  J. Sep. Sci. 2018, 41, 1199-1207 DOI:10.1002/jssc.201701068
  
  
• Tuma, J.; Kohout, M.: 
  Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation 
  RSC Adv. 2018, 8, 1174-1181 DOI:10.1039/c7ra12658a
  
  
• Kozmik, V.; Rodinová, E.; Prausová, T.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Mesogens with central naphthalene core substituted at various positions 
  Liq. Cryst. 2018, 45, 744-756 DOI: 10.1080/02678292.2017.1380238
  
  
•  Bajzíková, K.; Vesely, J.; Kozmik, V.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Thiophene central core for the design of bent-shaped liquid crystals 
  J. Mol. Liq. 2018, 267, 496-503 DOI:10.1016/j.molliq.2018.02.009
  
  
• Horcic, M.; Svoboda, J.; Novotná, V.; Pociecha, D.; Gorecka, E.:
  Bent-core dimers with top-to-bottom linkage between central units 
  RSC Adv. 2018, 8, 22974-22985 DOI: 10.1039/c8ra04108c
  
  
• Marz, M.; Kohout, M.; Nevesely, T.; Chudoba, J.; Prukala, D.; Nizinski, S.; Sikorski, M.; Burdzinski, G.; Cibulka, R.:
  Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control
  Org. Biomol. Chem. 2018, 16, 6809-6817 DOI:10.1039/C8OB01822G
  
  

2017

• Maixner, J.; Jurásek, B.; Kohout, M.; Kuchar, M.; Kacer, P.:
  X-ray powder diffraction data for (S)-Deschloroketamine hydrochloride, C₁₃H₁₈ClNO.
  Powder Diffr. 2017, 32, 193-195. DOI:10.1017/S0885715617000586
  
  
• Bajzíková, K.; Svoboda, J.; Novotná, V.; Pociecha, D.; Gorecka E.:
  Bent-core mesogens with an aromatic unit at the terminal position
  New J. Chem. 2017, 41, 4672-4679 DOI: 10.1039/C6NJ03908A
  
  
• Žurek, J.; Svobodová, E.; Šturala, J.; Dvořáková, 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
  Tetrahedron Asymmetry 2017, asap DOI:10.1016/j.tetasy.2017.10.029
  
  

• Dobrovolny, K.; Ulbrich, P.; Svecova, M.; Rimpelova, S.; Malincik, J.; Kohout, M.; Svoboda, J.; Bartunek, V.: 
  Copper nanoparticles in glycerol-​polyvinyl alcohol matrix: In situ preparation, stabilization and antimicrobial activity
  Journal of Alloys and Compounds 2017, 697, 147-155 DOI:10.1016/j.jallcom.2016.12.144
  
  
• Kolderova, N.; Nevesely, T.; Sturala, J.; Kuchar, M.; Holakovsky, R.; Kohout, M.:
  Enantioseparation of chiral sulfoxides on amylose-​based columns: comparison of normal phase liquid chromatography and supercritical fluid chromatography
  Chromatographia 2017, 80, 547-557 DOI: 10.1007/s10337-016-3234-6
  
  
• Kohout, M.; Alaasar, M.; Poryvai, A.; Novotna, V.; Poppe, S.; Tschierske, C.; Svoboda, J.: 
  Photosensitive bent-​core liquid crystals based on methyl substituted 3-​hydroxybenzoic acid
  RSC Advances 2017, 7, 35805-35813 DOI:10.1039/C7RA05632J
  
  
• Wolrab, D.; Fruehauf, P.; Gerner, C.; Kohout, M.; Lindner, W.: 
  Consequences of transition from liquid chromatography to supercritical fluid chromatography on the overall performance of a chiral zwitterionic ion-​exchanger
  Journal of Chromatography A 2017, 1517, 165-175 DOI:10.1016/j.chroma.2017.08.022
  
  
• Pallova, L.; Kozmik, V.; Kohout, M.; Svoboda, J.; Novotna, V.; Pociecha, D.: 
  Bent-​core liquid crystals with a 2-​substituted 3-​hydroxybenzoic acid central core
  Liquid Crystals 2017, 44, 1306-1315 DOI: 10.1080/02678292.2016.1276981
  
  

• Tlusty, M.; Slavik, P.; Kohout, M.; Eigner, V.; Lhotak, P.:
  Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring
  Org. Lett. 2017, 19, 2933-2936 DOI:10.1021/acs.orglett.7b01170
  
  
• Miksatko, J.; Eigner, V.; Kohout, M.; Lhotak, P.:
  Regio-/stereoselective Formation of Monosulfoxides from Thiacalix[4]arenes in All Possible Conformations
  Tetrahedron Letters 2017, 58, 1687–1691 DOI:10.1016/j.tetlet.2017.03.043
  
  
• Horčic, M.; Kohout, M.; Svoboda, J.; Novotna, V.; Pociecha, D.; Gorecka, E.:
  Core-to-core Dimers Forming Switchable Mesophase
  Chem.  Commun. 2017, 53, 2721-2724 DOI:10.1039/C6CC09983A
  
  
• März, M.; Chudoba, J.; Kohout, M.; Cibulka, R.:
  Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light
  Org. Biomol. Chem. 2017, 15, 1970-1975 DOI:10.1039/C6OB02770A

2016

• 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 system
  J. Mater. Chem. C 2016, 4, 11540-11547 DOI:10.1039/C6TC04346A
  
  
• Tůma, J.; Kohout, M.; Svoboda, J.; Novotná, 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
  Liq. Cryst. 2016, 43, 1889-1900 DOI:10.1080/02678292.2016.1230789
  
  
• Kohout, M.; Vandenbussche, J.; Roller, A.; Tůma, J.; Boqaerts, J.; Bultinck, P.; Herrebout, W.; Lindner, W.:
  Absolute configuration of the antimalarial erythro-mefloquine - vibrational dichroism and X-ray diffraction studies of mefloquine and its thiourea derivative
  RSC Advances 2016, 6, 81461-81465 DOI:10.1039/C6RA19367F 
  
  
• Kohout, M.; Bubnov, A.; Šťurala, J.; Novotná, V.; Svoboda, J.:
  Effect on alkyl chain length in the terminal ester group on mesomorphic properties of new chiral lactic acid derivatives
  Liq. Cryst. 2016, 43, 1472-1485 DOI:10.1080/02678292.2016.1185170
  
  
• Grecsó, N.; Kohout, M.; Carotti, A.; Sardella, R.; Natalini, B.; Fülöp, F.; Lindner, W.; Péter, A.; Ilisz, I.: 
  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
  J. Pharm. Biomed. Anal. 2016, 124, 164-173 DOI:10.1016/j.jpba.2016.02.043
  
  
• Wolrab, D.; Frühauf, 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
  J. Pharm. Biomed. Anal. 2016, 120, 306-315 DOI:10.1016/j.jpba.2015.12.023
  
  
• Tůma, J.; Kohout, M.; Svoboda, J.; Novotná, V.; Pociecha, D.: 
  Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core - Part II 
  Liq. Cryst. 2016, 43, 547-563 DOI: 10.1080/02678292.2015.1125535
  
  
• Slavik, P.; Kohout, M.; Böhm, S.; Eigner, V.; Lhotak, P.:
  Synthesis of Inherently Chiral Calixarenes via Direct Mercuration of the Partial Cone Conformation 
  Chem. Comm. 2016, 52, 2366-2360 DOI:10.1039/C5CC09388K

2015

• Trišović, N.; Antanasijević, J.; Tóth-Katona, T.; Kohout, M.; Salamonczyk, M.; Sprunt, S.; Jákli, A.; Fodor-Csorba, K.: Azo-containing asymmetric bent-core liquid crystals with modulated smectic phase RSC Adv. 2015, 5, 64886-64891. DOI: 10.1039/c5ra09764a
   
• 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 Tetrahedron 2015, 71, 2698-2707. DOI: 10.1016/j.tet.2015.03.037
   
• von Koschitzky, I.; Gerhardt, H.; Lämmerhofer, 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 Amino Acids 2015, 47, 1155-1166. DOI: 10.1007/s00726-015-1943-z
   
• Kohout, M.; Kozmík, V.; Slabochová, M.; Tůma, J.; Svoboda, J.; Novotná, V.; Pociecha, D.: Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core Liq. Cryst. 2015, 42, 87-103. DOI: 10.1080/02678292.2014.965232
   
• Kozmík, V.; Poznik, M.; Svoboda, J.; Frere, P.:
  Dithieno[3,2-b:2',3'-d]furan as a new building block for fused conjugated systems
  Tetrahedron Lett. 2015, 56, 6251-6253. DOI:10.1016/j.tetlet.2015.09.107
   
  

2014

• Lo Ch., Doucoure B. I., Aaron J.-J., Svoboda J., Kozmík V., Brochon J.-C., Henry H., Capochichi M.: Synthesis and optical properties of new fluorescent substituted thieno[3,2-b]indole derivatives. Spectrochim. Acta A, Molecular and Biomolecular Spectroscopy 2014, 120C, 47-54. DOI: 10.1016/j.saa.2013.09.134
   
  
• Kovářová A., Světlík S., Kozmík V., Svoboda J., Novotná V., Pociecha D., Gorecka E., Podoliak N.: Unusual polymorphism in new bent-shaped liquid crystals with hydroxybiphenylcarboxylic acid central unit. Beil. J. Org. Chem. 2014, 10, 794-807. DOI: 10.3762/bjoc.10.75
    
• Olšinová M., Jurkiewicz P., Pozník M., Šachl R., Prausová T., Hof M., Kozmík V., Teplý F., Svoboda J., Cebecauer M.: Di- and tri-oxalkyl derivatives of boron dipyrromethene (BODIPY) rotor dye in lipid bilayers. PhysChemChemPhys. 2014, 16, 10688-10697. DOI: 10.1039/C4CP00888J
   
  
• Hetteger H., Kohout M., Mimini V., Lindner W.: Novel carbamoyl type quinine and quinidine based chiral anion exchangers implementing alkyne-azide cycloaddition immobilization chemistry. J. Chromatogr. A 2014, 1337, 85-94. DOI: 10.1016/j.chroma.2014.02.026

2013

• Machara A., Svoboda J.: Thiophenium-ylides: synthesis and reactivity. Chem. Papers 2013, 67, 59-65. DOI: 10.2478/s11696-012-0222-7
   
  
• Kohout M., Tůma J., Svoboda J., Novotná V., Gorecka E., Pocicha D.: 3-Hydroxycinnamic acid - a new central core for the design of bent-shaped liquid crystals. J. Mater. Chem. C 2013, 1, 4962-4969. DOI: 10.1039/C3TC30664J
   
  
• Novotná V., Baumeister U., Kohout M., Svoboda J.: Mesomorphic properties of a bent-shaped liquid crystalline monomer. Phase Trans. 2013, 86, 503-515. DOI: 10.1080/01411594.2012.702279
   
  
• Horčic M., Kozmík V., Svoboda J., Novotná 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: 10.1039/C3TC31593B
   
  
• Seidler A., Svoboda J., Dekoj V., Chocholoušová J., Vacek J., Stará I. G., Starý I.: The synthesis of pi-electron molecular rods with a thiophene or thieno[3,2-b]thiophene core units and sulphur alligator clips. Tetrahedron Lett. 2013, 54, 2795-2798. DOI: 10.1016/j.tetlet.2013.03.084
   
  
• Novotná V., Glogarová M., Kozmík V., Svoboda J., Hamplová V., Kašpar M., Pociecha D.: Frustrated phases induced in binary mixtures of hockey-stick and chiral rod-like mesogens. Soft Matter 2013, 9, 647-653. DOI: 10.1039/C2SM27194J
   
  
• Wolrab D., Macíková 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. J. Chromatogr. A 2013, 1317, 59-66. DOI: 10.1016/j.chroma.2013.08.037
   
  
• Gargano A. F. G., Buchinger S., Kohout M., Lindner W., Lämmerhofer M.: Single-step Ugi multicomponent reaction for the synthesis of phosphopeptidomimetics. J. Org. Chem. 2013, 78, 10077-10087. DOI: 10.1021/jo401372x
   
  
• 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. Anal. Bioanal. Chem. 2013, 405, 8011-8026. DOI: 10.1007/s00216-013-6932-z
   
  
• Gargano A. F. G., Kohout M., Macíková P., Lämmerhofer M., Lindner W.: Direct high-performance liquid chromatographic separation of free alpha-, beta- and gamma-aminophosphonic acids employing cinchona-based chiral zwitterionic ion exchangers. Anal. Bioanal. Chem. 2013, 405, 8027-8038. DOI: 10.1007/s00216-013-6938-6
   
  
• Wolrab D., Frühauf P., Kohout M., Lindner W.: Click chemistry immobilization strategies in the development of strong cation exchanger chiral stationary phases for HPLC. J. Sep. Sci. 2013, 36, 2826-2837. DOI: 10.1002/jssc.201300559
   
  
• Wolrab D., Kohout M., Boras M., Lindner W.: Strong cation exchange-type chiral stationary phase for enantiseparation of chiral amines in subcritical fluid chromatography. J. Chromatogr. A 2013, 1289, 94-104. DOI: 10.1016/j.chroma.2013.03.018

2012

• Mallet C., Savitha G., Allain M., Kozmík 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.
• Kovářová A., Kozmík V., Svoboda J., Novotná V., Glogarová M., Pociecha D.: Naphthalene-based bent-shaped liquid crystals with a semifluorinated terminal chain. Liq. Cryst. 2012, 39, 755-767.
• Kozmík V., Horčic M., Svoboda J., Novotná V., Pociecha D.: 3-Aminophenol based bent-shaped liquid crystals with an amide linking group. Liq. Cryst. 2012, 39, 943-955.
• Kohout M., Kählig 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.

2011

• Kohout M., Svoboda J., Novotná 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.
• Kozmík V., Henke A., Řehová L., Kurfürst M., Slabochová M., Svoboda J., Novotná V., Glogarová M.: Liquid crystalline benzothiophene derivatives. Part 2. 2,5-Disubstituted benzothiophenes. Liq. Cryst. 2011, 38, 1245-1261.
• Aaron J.-J., Párkányi C., Adenier A.,Potin C., Zajíčková Z., Martínez O. R., Svoboda J., Pihera P., Váchal P.: Fluorescence properties and dipole moments of novel fused thienobenzofurans. Solvent and structural effects. J. Fluorescence 2011, 21, 2133-2141.

2010

• Kovářová A., Svoboda J., Novotná V., Glogarová M., Salamonczyk M., Pociecha D., Gorecka E.: [2]Benzothiophene bent-shaped liquid crystals. Liq. Cryst. 2010, 37, 1501-1513.
• Kozmík V., Polášek P., Seidler A., Kohout M., Svoboda J., Novotná V., Glogarová 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.
• Kohout M., Svoboda J., Novotná V., Glogarová M., Pociecha D.: Non-symmetrical bent-shaped liquid crystals with five ester groups. Liq. Cryst. 2010, 37, 987-996.
• Obadović D. Ž., Vajda A., Jákli A., Menyhárd A., Kohout M., Svoboda J., Stojanović M., Éber N., Galli G., Fodor-Csorba K.: Mesophase behaviour of binary mixtures of bell-shaped and calamitic compounds. Liq. Cryst. 2010, 37, 527-536.
• Kohout M., Chambers M., Vajda A., Galli G., Domján A., Svoboda J., Bubnov A., Jákli A., Fodor-Csorba K.: Properties of non-symmetric bent-core liquid crystals with variable flexible chain length. Liq. Cryst. 2010, 37, 537-545.
• Ledesma A. E., Contreras C., Svoboda J., Vektariane A., Brandán S. A.: Theoretical structures and experimental vibrational spectra of isomeric benzofused thieno[3,2-b]furan compounds. J. Mol. Struc. 2010, 967, 159-165.
• Žurek J., Cibulka R., Dvořáková 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.
• Weissflog W., Pelzl G., Kresse H., Baumeister U., Brand K., Schröder 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.
• Lô C., Aaron J.-J., Kozmík 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.
• Glogarová M., Hampl F.,Lejček L., Novotná 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.

2009

• Kohout M., Svoboda J., Novotná V., Pociecha D., Glogarová 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.
• Machara J., Kozmík V., Pojarová M., Dvořáková H., Svoboda J.: Preparation and rearrangement study of novel thiophenium- and selenophenium-ylides. Collect. Czech. Chem. Commun. 2009, 74, 785-798.
• 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.
• Vaupotić N., Szydlowska J., Salamonczyk M., Kovářová 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)
• Salamonczyk M., Kovářová A., Svoboda J., Pociecha D., Gorecka E.: Switchable fluorescent liquid crystals. Appl. Phys. Lett. 2009, 95, 171901.

2008

• Kurfürst M., Kozmík V., Svoboda J., Novotná V., Glogarová M.: Liquid crystalline benzothiophene derivatives. Liq. Cryst. 2008, 35, 21.
• Sedlák M., Drabina P., Lánský 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.
• Lô C., Adenier A., Maurel F., Aaron J.-J., Kozmík 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.
• Novotná V., Žurek J., Kozmík V., Svoboda J., Glogarová M.: Novel hockey-stick mesogens with the nematic, synclinic and anticlinic smectic C phase sequence. Liq. Cryst. 2008, 35, 1023.
• Lô 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.
• Obadović D.Z., Vajda A., Jákli A., Kohout M., Stojanović M., Éber N., Fodor-Csorba K., Galli G.: Phase Sequences of Mixtures Formed by Bell-shaped and Calamitic Compound. J. Res. Phys. 2008, 32, 69-74.

2007

• Machara A., Pojarová M., Svoboda J.: Synthesis and cycloaddition reaction of 3-vinylthieno[3,2-b][1]benzothiophene. Collect. Czech. Chem. Commun. 2007, 72, 952-964.

2006

• Kozmík V., Kovářová A., Kuchař M., Svoboda J., Novotná V., Glogarová M., Kroupa J.: Novel polymerizable bent-shaped monomeric molecules. Liq. Cryst., 2006, 33, 41.
• Kozmík V., Košata B., Svoboda J., Kuchař M.: A study of 5-nitroindole alkylation Collect. Czech. Chem. Commun., 2006, 71, 679.
• Lô C., Adenier A., Chane-Ching K., Maurel F., Aaron J. J., Košata 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.
• Černovská K., Košata B., Svoboda J., Novotná V., Glogarová 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.
• Aaron J.-J., Mézlová 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.