Journal of chromatography. A 2014-10-10

Direct high-performance liquid chromatographic enantioseparation of secondary amino acids on Cinchona alkaloid-based chiral zwitterionic stationary phases. Unusual temperature behavior.

István Ilisz, Zsanett Gecse, Zoltán Pataj, Ferenc Fülöp, Géza Tóth, Wolfgang Lindner, Antal Péter

Index: J. Chromatogr. A. 1363 , 169-77, (2014)

Full Text: HTML

Abstract

Two chiral stationary phases containing a quinine- or a quinidine-based zwitterionic ion-exchanger as chiral selector were applied for the enantioseparation of 27 unusual cyclic secondary α-amino acids. The effects of the nature and concentration of the bulk solvent, the acid and base additives, the structures of the analytes and temperature on the enantioresolution were investigated. To study the effects of temperature and to obtain thermodynamic parameters, experiments were carried out at constant mobile phase compositions in the temperature range -5 to 55 °C. The thermodynamic parameters indicated that in most cases the separations were enthalpy-driven, but some entropy-driven separations were also observed. The sequence of elution of the enantiomers was determined in most cases.Copyright © 2014 Elsevier B.V. All rights reserved.

Related Compounds

Structure Name/CAS No. Articles
Formic Acid Structure Formic Acid
CAS:64-18-6
Acetonitrile Structure Acetonitrile
CAS:75-05-8
Methanol Structure Methanol
CAS:67-56-1
acetic acid Structure acetic acid
CAS:64-19-7
L-Hydroxyproline Structure L-Hydroxyproline
CAS:3398-22-9
Triethylamine Structure Triethylamine
CAS:121-44-8
Ammonia Structure Ammonia
CAS:7664-41-7
Propylamine Structure Propylamine
CAS:107-10-8
Diethylamine Structure Diethylamine
CAS:109-89-7
Stanolone Structure Stanolone
CAS:521-18-6