๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Preparation and evaluation of a vancomycin-immobilized silica monolith as chiral stationary phase for CEC

โœ Scribed by Xiaoli Dong; Jing Dong; Junjie Ou; Yan Zhu; Hanfa Zou


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
306 KB
Volume
28
Category
Article
ISSN
0173-0835

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

Enantiomeric separations in CEC with the macrocyclic antibiotic vancomycin immobilized silica monolith as a chiral stationary phase are presented. The monolithic silica capillary columns were prepared by a solโ€“gel process in fusedโ€silica capillaries with an inner diameter of 50โ€…ฮผm and subsequently in situ immobilization of vancomycin as a chiral selector by reductive amination. Enantioselectivity was obtained for eight pairs of enantiomers in nonaqueous polar organic or aqueous mobile phases and most of them were baselineโ€separated with high column efficiencies. It was observed that the organic modifier ratio (MeOH/ACN) in the polar organic mobile phase played a significant role in controlling the resolution and efficiency of the enantiomers. In enantiomeric separation of propranolol, repeatability for column efficiency and resolution in the nonaqueous mobile phase was given in terms of RSD values at 1.1 and 2.3% (nโ€…=โ€…5) for runโ€toโ€run injections and 7.2 and 9.6% (nโ€…=โ€…5) for columnโ€toโ€column testing while repeatability for the separation of thalidomide in the aqueous mobile phase was given in terms of RSD values at 1.5, 2.8% and 6.1, 10.5%, respectively.


๐Ÿ“œ SIMILAR VOLUMES


New Stationary Phase Prepared by Immobil
โœ Silva, Cesar R. ;Jardim, Isabel C. S. F. ;Airoldi, Claudio ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 91 KB ๐Ÿ‘ 2 views

Chromatographic silica (10 lm) was chemically modified with the silylating agent: [3-(2-aminoethyl)aminopropyl]trimethoxysilane (AEAPTS). The reaction product was characterized by elemental analysis and infrared and 13 C and 29 Si NMR spectra. The chemically modified silica was treated with Cu(II) i

(S)-Leucine and [(S)-1-(1-Naphthyl)ethyl
โœ Anna Iuliano; Emanuele Attolino; Piero Salvadori ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 295 KB ๐Ÿ‘ 3 views

Two selectors derived from [(S)-1-(1-naphthyl)ethyl]amine and (S)-leucine have been chemically bonded to one another and the resulting chiral auxiliary linked covalently to silica gel, to produce a new chiral stationary phase (CSP) for the HPLC resolution of enantiomers. The CSP is able to separate