Synthesis of covalently bonded cellulose derivative chiral stationary phases with a bifunctional reagent of 3-(triethoxysilyl)propyl isocyanate


Autoria(s): Chen, XM; Liu, YQ; Qin, F; Kong, L; Zou, HF
Data(s)

29/08/2003

Resumo

A bifunctional reagent of 3-(triethoxysilyl)propyl isocyanate (TEPI) was initially adopted as a spacer reagent to prepare the bonded types of chiral stationary phases (CSPs) with cellulose derivatives. The silica-based CSPs were chemically prepared with non-regioselective and regioselective approaches and their chiral resolving capabilities were evaluated in terms of HPLC resolution of test enantiomers. It was observed that the chiral recognition capabilities of the non-regioselectively prepared CSPs were influenced by the amount of TEPI used. And also, the regioselectively prepared CSP generally showed a slightly higher resolution power than the non-regioselectively prepared CSP, while the non-regioselective procedures were highly advantageous to rapid preparation. In addition, chiral recognition of the prepared CSPs was affected by the properties of the used silica matrices. (C) 2003 Elsevier B.V. All rights reserved.

Identificador

http://159.226.238.44/handle/321008/83447

http://www.irgrid.ac.cn/handle/1471x/139106

Idioma(s)

英语

Fonte

陈小明;刘月启;秦峰;孔亮;邹汉法.Synthesis of covalently bonded cellulose derivative chiral stationary phases with a bifunctional reagent of 3-(triethoxysilyl)propyl isocyanate,Journal of Chromatography A,2003,1010():185-194

Palavras-Chave #chiral stationary phases #LC #enantiomer separation #cellulose #triethoxysilylpropyl isocyanate
Tipo

期刊论文