Chiral monolithic columns for enantioselective capillary electrochromatography prepared by copolymerization of a monomer with quinidine functionality.: 2.: Effect of chromatographic conditions on the chiral separations

被引:115
作者
Lammerhofer, M [1 ]
Svec, F
Fréchet, JMJ
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Vienna, Inst Analyt Chem, A-1090 Vienna, Austria
关键词
D O I
10.1021/ac000323d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The effect of chromatographic conditions on the performance of chiral monolithic poly(O-[2-(methacryloyloxy)-ethylcarbamoyl]-10,11-dihydroquinidine-co-ethylene dimethacrylate-co-2-hydroxyethyl methacrylate) columns in the capillary electrochromatography of enantiomers has been studied. The now velocity was found to be proportional to the pore size of the monolith and both the pH and the composition of the mobile phase. The length off both open and monolithic segments of the capillary column was found to exert a substantial effect on the run times. The use of monoliths as short as 8.5 cm and the "short-end" injection technique enabled the separations to be achieved in similar to 5 min despite the high retentitivity of the quinidine selector. Very high column efficiencies of close to 250 000 plates/m and good selectivities were achieved for the separations of numerous enantiomers using the chiral monolithic capillaries with the optimized chromatographic conditions.
引用
收藏
页码:4623 / 4628
页数:6
相关论文
共 56 条
[11]   Enantiomeric separations of cationic and neutral compounds by capillary electrochromatography with β-cyclodextrin-bonded charged polyacrylamide gels [J].
Koide, T ;
Ueno, K .
ANALYTICAL SCIENCES, 1999, 15 (08) :791-794
[12]   Enantiomeric separations of cationic and neutral compounds by capillary electrochromatography with charged polyacrylamide gels incorporating chiral selectors [J].
Koide, T ;
Ueno, K .
ANALYTICAL SCIENCES, 1998, 14 (05) :1021-1023
[13]  
Koide T, 2000, HRC-J HIGH RES CHROM, V23, P59
[14]   Enantioseparations in normal- and reversed-phase nano-high-performance liquid chromatography and capillary electrochromatography using polyacrylamide and polysaccharide derivatives as chiral stationary phases [J].
Krause, K ;
Girod, M ;
Chankvetadze, B ;
Blaschke, G .
JOURNAL OF CHROMATOGRAPHY A, 1999, 837 (1-2) :51-63
[15]  
Krause K, 1999, ELECTROPHORESIS, V20, P2772
[16]   Chiral anion exchangers applied to capillary electrochromatography enantioseparation of oppositely charged chiral analytes:: investigation of stationary and mobile phase parameters [J].
Lämmerhofer, M ;
Tobler, E ;
Lindner, W .
JOURNAL OF CHROMATOGRAPHY A, 2000, 887 (1-2) :421-437
[17]  
Lammerhofer M, 1998, AM LAB, V30, P71
[18]   High-efficiency chiral separations of N-derivatized amino acids by packed-capillary electrochromatography with a quinine-based chiral anion-exchange type stationary phase [J].
Lämmerhofer, M ;
Lindner, W .
JOURNAL OF CHROMATOGRAPHY A, 1998, 829 (1-2) :115-125
[19]   Quinine and quinidine derivatives as chiral selectors .1. Brush type chiral stationary phases for high-performance liquid chromatography based on cinchonan carbamates and their application as chiral anion exchangers [J].
Lammerhofer, M ;
Lindner, W .
JOURNAL OF CHROMATOGRAPHY A, 1996, 741 (01) :33-48
[20]  
LAMMERHOFER M, IN PRESS J CHROMAT A