Comparison of monomeric and polymeric amino acid based surfactants for chiral separations

被引:37
作者
Billiot, FH
Billiot, EJ
Warner, IM [1 ]
机构
[1] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
[2] Texas A&M Univ, Dept Phys & Life Sci, Corpus Christi, TX 78412 USA
关键词
enantiomer separations; enantiomer separation; background electrolylte composition; pseudostationary phases; surfactants; binaphthol; lorazepam; binaphthyl dihydrogenphosphate; temazepam; propanolol; amino acids; peptides;
D O I
10.1016/S0021-9673(01)00865-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To better understand chiral recognition with polymeric amino acid based surfactants, the chromatographic performance of 18 monomeric and polymeric surfactants were compared for chiral analytes with various charge states and hydrophobicities. In this study, four amino acids (glycine, L-alanine, L-valine, and L-leucine) were chosen, and all possible combinations of the chiral single aminoacid and dipeptide surfactants were synthesized. The results indicate that polymeric surfactants usually provide better chiral resolution for enantiomers of lorazepam, temazepam, 1,1 ' -bi-2-naphthol, and propranolol as compared to monomeric surfactants. In contrast, monomers perform better for chiral recognition of the 1,1 ' -bi-2-naphthyl-2,2 ' -diyl hydrogenphosphate enantiomers. (C) 2001 Elsevier Science BN. All rights reserved.
引用
收藏
页码:329 / 338
页数:10
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