How mobile phase composition and column temperature affect enantiomer elution order of liquid crystals on amylose tris(3‐chloro‐5‐methylphenylcarbamate) as chiral selector

• Published in: Electrophoresis Vol. 42; no. 17-18; pp. 1844 - 1852
• Main Authors: Vaňkátová, Petra, Kubíčková, Anna, Kalíková, Květa
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 01-09-2021
• Subjects: Acetonitrile; Additives; Amylose - analogs & derivatives; Chlorine; Chromatography, High Pressure Liquid; Elution; Enantiomer elution order; Enantiomers; Enantioseparation; Ions; Liquid Crystals; Phase composition; Phenylcarbamates; Polysaccharide chiral stationary phase; Silica gel; Silicon dioxide; Solvents; Stereoisomerism; Temperature; Enantiomer elution order; Enantioseparation; Polysaccharide chiral stationary phase; Liquid crystals
• ISSN: 0173-0835; 1522-2683
• DOI: 10.1002/elps.202000350

A comprehensive study into the effects of mobile phase composition and column temperature on enantiomer elution order was conducted with a set of chiral rod‐like liquid crystalline materials. The analytes were structurally similar and comprised variances such as length of terminal alkyl chain, presence of chlorine, number of phenyl rings, and type of chiral center. Experiments were carried out in polar organic and reversed‐phase modes using amylose tris(3‐chloro‐5‐methylphenylcarbamate) immobilized on silica gel as the chiral stationary phase. For all liquid crystals, reversal of elution order of enantiomers was observed based on type of used cosolvent and/or its content in the mobile phase; for some of the liquid crystals a temperature‐induced reversal was also observed. Both linear and nonlinear dependencies of natural logarithm of enantioselectivity on temperature were found. Tested mobile phases comprised pure organic solvents and binary and tertiary mixtures of acetonitrile with organic solvents and/or water. Effect of acidic/basic mobile phase additives was also tested. Effect of structure of chiral selector is briefly discussed.