Improved Procedure for Preparation of Covalently Bonded Cellulose Tris-phenylcarbamate Chiral Stationary Phases
✍ Scribed by Qin Feng; Chen Xiao-Ming; Liu Yue-Qi; Zou Han-Fa; Wang Jun-De
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 69 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0256-7660
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The classical method for preparation of covalently boned cellulose derivative chiral stationary phases (CSP) with diisocyanate as spacer was improved. Diisocyanate was firstly allowed to react with 3‐aminopropyltriethoxysilane, and the resulting product was then applied as the spacer reagent to immobilize cellulose derivatives onto silica gel. Influences of the amount and the length of the spacer on the optical resolution ability of the CSP were investigated. Comparing improved procedure to classical diisocyanate method, the cross‐linking between the glucose units of the cellulose derivatives was avoided to the most extent. With the improved procedure, regio‐nonselective ways could be adopted to prepare covalently bonded CSP, which showed an advantage for the rapid preparation.
📜 SIMILAR VOLUMES
## Abstract A novel cellulose tris(__N__‐3,5‐dimethylphenylcarbamate) (CDMPC) chiral stationary phase (CSP) was prepared by coating CDMPC on TiO~2~/SiO~2~, which was prepared by coating titania nanoparticles on silica through a self‐assemble technique. At first, 2‐hydroxyl‐phenyl acetonitrile and _
## Abstract A novel chiral stationary phase based on chitosan covalently bonded onto silica gels has been prepared and used for the separation of various α‐amino acid enantiomers as well as α‐hydroxycarboxylic acid enantiomers by chiral ligand‐exchange chromatography with copper(II) as a complexing