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纤维素2,3-位和2,3,6-位苯基氨基甲酸酯手性固定相的选择性研究
引用本文:常银霞,周玲玲,袁黎明. 纤维素2,3-位和2,3,6-位苯基氨基甲酸酯手性固定相的选择性研究[J]. 色谱, 2007, 25(2): 203-206
作者姓名:常银霞  周玲玲  袁黎明
作者单位:1.Faculty of Chemistry and Chemical Engineering, Yunnan Normal University, Kunming 650092, China; 2.College of Chemistry and Material Science, Shanxi Normal University, Linfen 041000, China
基金项目:国家自然科学基金;教育部高等学校优秀青年教师教学科研奖励计划;云南省自然科学基金
摘    要:合成了纤维素-2,3,6-三苯基氨基甲酸酯、纤维素-2,3-二苯基氨基甲酸酯、纤维素-2,3,6-三(3,5-二甲基苯基氨基甲酸酯)和纤维素-2,3-二(3,5-二甲基苯基氨基甲酸酯)4种纤维素衍生物手性固定相,用正己烷-异丙醇(体积比为9∶1)混合液作流动相,对9种手性化合物进行了高效液相色谱拆分。实验结果表明:对所测的9个样品,纤维素-2,3-二苯基氨基甲酸酯的手性选择性大大好于纤维素-2,3,6-三苯基氨基甲酸酯;而纤维素-2,3-二(3,5-二甲基苯基氨基甲酸酯)与纤维素-2,3,6-三(3,5-二甲基苯基氨基甲酸酯)的分离因子针对不同的对映体各有优点,但前者通常具有更小的保留因子,可以缩短一定的分析时间。

关 键 词:高效液相色谱  手性固定相  纤维素衍生物  
文章编号:1000-8713(2007)02-0203-04
收稿时间:2006-05-30
修稿时间:2006-05-30

Study on Enantioselectivity of Celluloses Derived by Phenylcarbamate at 2,3- or 2,3,6-Positions
CHANG Yinxia,ZHOU Lingling,YUAN Liming. Study on Enantioselectivity of Celluloses Derived by Phenylcarbamate at 2,3- or 2,3,6-Positions[J]. Chinese journal of chromatography, 2007, 25(2): 203-206
Authors:CHANG Yinxia  ZHOU Lingling  YUAN Liming
Affiliation:1.Faculty of Chemistry and Chemical Engineering, Yunnan Normal University, Kunming 650092, China; 2.College of Chemistry and Material Science, Shanxi Normal University, Linfen 041000, China
Abstract:Cellulose-2, 3, 6-trisphenylcarbamate, cellulose-2, 3-bisphenylcarbamate, cellulose2,3,6-tris(3,5-dimethylphenylcarbamate) and cellulose-2,3-bis(3,5-dimethylphenylcarbamate) were synthesized and respectively coated on silica gel as chiral stationary phases for high performance liquid chromatography (HPLC). Nine pairs of enantiomers, which are ( +/- )-phenyl-1, 2-ethanediol, ( +/- )-2-phenyl-1 -propanol, DL-alpha-methylbenzylamine, DL-mandelic acid, ( +/- ) -1-(1-naphthyl) ethanol, ( +/- ) -propranolol, ( +/- ) -3-benzyloxy-1, 2-propanediol, DL-tyrosine and ( +/- ) -di-O, O-p-toluyl-D-tartaric acid, were separated using hexane-isopropanol as mobile phase on the columns packed with the chiral stationary phases. For comparative reasons, the ratio of hexane/isopropanol in the eluent was kept at 9: 1 (v/v) in all experiments, and the chromatographic separations were performed at 30 degrees C with a flow rate of 0. 5 mL/min. All the test solutes were detected at 254 nm. The results showed that enantioseparation of cellulose-2,37bisphenylcarbamate was better than cellulose-2,3,6-trisphenylcarbamate for the test enantiomers, and cellulose-2,3-bis (3 ,5-dimethylphenylcarbamate) had low retention factors and short analysis times for most enantiomers and good separation factors for some racemates compared to cellulose-2,3,6-tris(3,5-dimethylphenylcarbamate).
Keywords:cellulose derivatives  chiral stationary phases  high performance liquid chromatography(HPLC)
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