首页 | 本学科首页   官方微博 | 高级检索  
     检索      

微径高效液相色谱法分离三唑类手性化合物的对映体
引用本文:江正瑾,高如瑜,张锴,张智超,王琴孙,阎超.微径高效液相色谱法分离三唑类手性化合物的对映体[J].色谱,2001,19(3):253-255.
作者姓名:江正瑾  高如瑜  张锴  张智超  王琴孙  阎超
作者单位:[1]南开大学元素有机化学国家重点实验室,天津300071 [2]UnimicroTechnologies,Inc,4713FirstStreet,Pleasanton,CA
基金项目:国家自然科学基金青年基金(批准号:29907002)资助
摘    要: 采用微径高效液相色谱技术在手性纤维素色谱柱上分离了一系列 1 1,2 ,4 三唑类手性化合物。比较了微径液相色谱与传统液相色谱的分离结果 ,研究了化合物的苯环上不同取代基及取代基位置对分离的影响 ,并探讨了分离机理。

关 键 词:微径高效液相色谱  高效液相色谱  对映体分离  三唑类手性农药
文章编号:1000-8713(2001)03-0253-03
修稿时间:2000年9月28日

Enantiomeric Separations of 1-1,2,4-Triazole Compounds by Micro-High Performance Liquid Chromatography
JIANG Zheng jin ,GAO Ru yu ,ZHANG Kai ,ZHANG Zhi chao ,WANG Qin sun ,YAN Chao.Enantiomeric Separations of 1-1,2,4-Triazole Compounds by Micro-High Performance Liquid Chromatography[J].Chinese Journal of Chromatography,2001,19(3):253-255.
Authors:JIANG Zheng jin  GAO Ru yu  ZHANG Kai  ZHANG Zhi chao  WANG Qin sun  YAN Chao
Abstract:The enantiomeric separations of sixteen novel 1-1,2,4-triazole chiral compounds were investigated by micro-HPLC with a 200 mm x 100 microns i.d. capillary chiral OD column. The detection was performed at 223 nm. The mobile phase was a mixture of iso-propyl alcohol and n-hexane(20:80, V/V) at a flow rate of 30 microL/min and column head pressure of 6.9 MPa. Some of the enantiomers could be separated on baseline. In comparing with the separation results by the conventional HPLC method, the micro-HPLC method had the advantages of high-speed, economy, environmental friendliness etc. The effect of solute structure on enantio-selectivity was investigated and the chiral recognition mechanism was also discussed. It was found that the main separation mechanisms involve the pi-pi association and inclusion between the substituent R and the spiral pocket of OD-CSP.
Keywords:micro  high performance liquid chromatography  high performance liquid chromatography  enantiomer separation  1  1  2  4  triazole chiral compound  
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《色谱》浏览原始摘要信息
点击此处可从《色谱》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号