Synthesis of chiral stationary phases via bonding β-cyclodextrin with α-schiff base and chromatographic performance

Min Fang, Zhi Ming Zhou*, Ai Qin Luo

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Two chiral stationary phases (BCDs and YBCDs) were prepared by bonding β-cyclodextrin derivative with α-Schiff base group from β-cyclodextrin monoaldehyde to the silica gel via 3-glyci-dyloxypropyltrimethoxysilane as a coupling agent. Using acetonitrile-TEAA as mobile phase, good enantiomeric resolutions were obtained for DL-aminoacide on BCDs and YBCDs, including Leucine, Threonine and Valine. It is also observed that the higher separation factor of threonine was at pH 7.11 for both of the column, and the optimal column temperatures of Leucine appeared at 30°C or 40°C, respectively for YBCDs and BCDs.

Original languageEnglish
Pages (from-to)1443-1445
Number of pages3
JournalKao Teng Hsueh Hsiao Hua Heush Hsueh Pao/ Chemical Journal of Chinese Universities
Volume26
Issue number8
Publication statusPublished - Aug 2005

Keywords

  • HPLC
  • Schiff base
  • β-Cyclodextrin

Fingerprint

Dive into the research topics of 'Synthesis of chiral stationary phases via bonding β-cyclodextrin with α-schiff base and chromatographic performance'. Together they form a unique fingerprint.

Cite this