Enantiomer separation by capillary electrochromatography on a cyclodextrin-modified monolith
✍ Scribed by Dorothee Wistuba; Volker Schurig
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 157 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0173-0835
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✦ Synopsis
Enantiomer separation by capillary electrochromatography on a cyclodextrinmodified monolith
A chiral monolithic stationary phase was prepared by packing a capillary with bare porous silica and sintering the silica bed at high temperature. The resulting silica monolith was polymer-coated with Chirasil-Dex, a permethylated b-cyclodextrin covalently linked via an octamethylene spacer to dimethylpolysiloxane. Subsequently, Chirasil-Dex was thermally immobilized on the silica support and a chiral monolith of very high stability (30 kV, more than 400 bar pressure) was obtained. The enantiomer separation of various chiral compounds by monolithic (rod) capillary electrochromatography (rod-CEC) was feasible. This method was compared with capillary liquid chromatography (LC) in a single-column mode using unified equipment. About two to three times higher efficiency was found in the rod-CEC mode as compared to rod-LC. The influence of pressure-driven flow support on efficiency, resolution, elution time and baseline stability was investigated. The amount and nature of organic modifier strongly influences efficiency and resolution.
📜 SIMILAR VOLUMES
## Abstract Three new chiral selectors, 6‐__tert__‐butyldimethylsilyl‐2,3‐diethyl‐a‐cyclodextrin, 6‐__tert__‐butyldimethylsilyl‐2,3‐diethyl‐ and dipropyl‐β‐cyclodextrin (TBDE‐α‐CD, TBDE‐β‐CD, TBDP‐β‐CD) were synthesized and tested as chiral stationary phases in capillary gas chromatography. TBDE‐β‐