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Reference type: Conference Proceeding
Authors: Dong HX, Tong F, Li JQ, Wang ZX, Wang YH, Shen XD
Publication date: 2010
Article title: Chiral resolution of racemic ()-1,1'-Bi (2-naphthol) by use of molecularly imprinted polymers.
Page numbers: 150-159
DOI: 10.4028/www.scientific.net/AMR.150-151.150

Proceedings title: Advanced Materials Research
Editors: Liu XH, Jiang ZY, Han JT
Publisher: Scientific.net
ISBN: ISSN: 10226680 ISBN: 978-087849201-5
Volume number: 150-151
Conference information: Manufacturing Processes and Systems

Abstract: Polymers imprinted with (S)-(-)-1,1'-bi (2-naphthol) and (R)-(+)-1,1'-bi (2-naphthol) have been prepared by non-covalent imprinting. A combinational procedure was used to optimize the functional monomer and crosslinker. A copolymer of 2-vinylpyridine and divinylbenzene resulted in the best chiral recognition. The ratio of template to functional monomer and solvent in the pre-polymerization mixture were also optimized. The imprinted polymers were used as stationary phases in high-performance liquid chromatography (HPLC). The molecularly imprinted polymers (MIPs) were more selective when prepared using a less polar solvent. Effective separations of the enantiomers of racemic ()-1, 1'-Bi (2-naphthol) were achieved by use of acetonitrile as mobile phase; no cross-selectivity was observed. Interactions between functional monomers and template were investigated by 1H NMR spectroscopy. The results suggest that hydrogen-bonding between the functional monomer and the template and π-π stacking interaction between the cross-linker and the template may contribute to chiral recognition. (2011) Trans Tech Publications
Template and target information: (S)-(-)-1,1'-bi (2-naphthol), (R)-(+)-1,1'-bi (2-naphthol)
Author keywords: ()-1,1'-Bi (2-naphthol), 1H NMR, high performance liquid chromatography, Molecularly imprinted polymers


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