## Abstract Naphthylcarbamate‐substituted (3‐(2‐O‐β‐cyclodextrin)‐2‐hydroxypropoxy)‐propylsilyl‐appended silica gel (NSCD‐HPS) has been synthesized via a convenient liquid‐solid phase reaction on a silica gel surface. The chromatographic behavior of NSCD‐HPS in high‐performance liquid chromatograph
Application of bromoacetate-substituted β-CD-bonded silica particles as chiral stationary phase for HPLC
✍ Scribed by Sennappan K. Thamarai Chelvi; E. L. Yong; Yinhan Gong
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 323 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
Abstract
Bromoacetate‐substituted [3‐(2‐O‐β‐cyclodextrin)‐2‐hydroxypropoxy]propylsilyl‐appended silica particles (BACD‐HPS), an important and useful synthetic intermediate for preparation of novel types of macrocycles‐capped β‐CD‐bonded silica particles including crown ether/cyclam/calix[4]arene‐capped β‐CD‐bonded silica particles, have been prepared and used as chiral stationary phase for HPLC. This synthetic stationary phase is characterized by means of elemental analysis. For the first time, the chromatographic behavior of BACD‐HPS was systematically evaluated with several disubstituted benzenes and some chiral drug compounds under both normal and RP conditions in HPLC. The results show that BACD‐HPS has excellent selectivity for the separation of aromatic positional isomers and chiral isomers of some drug compounds when used as stationary phase in HPLC.
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## Abstract Perphenylcarbamoylated β‐cyclodextrin bonded‐silica particles (5 μm) were packed into 75‐μm fused‐silica capillaries, and used for the enantiomer separation of neutral and basic solutes by pressure‐assisted capillary electrochromatography. Triethylammonium acetate and phosphate buffer w