Enantiorecognition ability of different chiral selectors for separation of liquid crystals in supercritical fluid chromatography, critical evaluation

0534674 - FZÚ 2021 RIV NL eng J - Článek v odborném periodiku
Vaňkátová, Petra - Folprechtová, D. - Kalíková, K. - Kubíčková, A. - Armstrong, D.W. - Tesařová, E.
Enantiorecognition ability of different chiral selectors for separation of liquid crystals in supercritical fluid chromatography, critical evaluation.
Journal of Chromatography A. Roč. 1622, July (2020), s. 1-8, č. článku 461138. ISSN 0021-9673. E-ISSN 1873-3778
Grant CEP: GA MŠMT(CZ) EF16_019/0000760
Grant ostatní: OP VVV - SOLID21(XE) CZ.02.1.01/0.0/0.0/16_019/0000760
Institucionální podpora: RVO:68378271
Klíčová slova: supercritical fluid chromatography * chiral stationary phases * liquid crystals * enantioseparation * additives
Obor OECD: Analytical chemistry
Impakt faktor: 4.759, rok: 2020
Způsob publikování: Omezený přístup
https://doi.org/10.1016/j.chroma.2020.461138

Comprehensive study of enantioselective potential of eight different chiral stationary phases for chiral liquid crystal-forming molecules was conducted. The tested columns were: (i) polysaccharide-based Trefoil AMY1, CEL1 and CEL2 and (ii) superficially porous particles packed TeicoShell, VancoShell, TagShell, DMP-MaltoShell, and NicoShell. Twenty racemic mixtures of rod-like liquid crystalline materials comprising three different types of chiral centres and various other structural differences were used. Mobile phases consisting of supercritical carbon dioxide and alcohol as cosolvent were used. Effect of acidic and/or basic additives on enantioselectivity was also evaluated. Chiral stationary phases based on polysaccharides were found to have the greatest enantioselective potential for rod-like molecules that form liquid crystals, followed by TeicoShell, which proved suitable for enantioseparation of non-halogenated liquid crystals with lactic acid-based chiral centre.

Trvalý link: http://hdl.handle.net/11104/0312849