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Reference type: Journal
Authors: Mukawa T, Goto T, Nariai H, Aoki Y, Imamura A, Takeuchi T
Article Title: Novel strategy for molecular imprinting of phenolic compounds utilizing disulfide templates.
Publication date: 2003
Journal: Journal of Pharmaceutical and Biomedical Analysis
Volume: 30
Issue: (6)
Page numbers: 1943-1947.
DOI: 10.1016/S0731-7085(02)00538-1

Abstract: A molecularly imprinted polymer was synthesized by using allyl phenyl disulfide as a template. The mixture of allyl phenyl disulfide, divinylbenzene, and 2,2'-azobis(isobutyronitrile) in chloroform was polymerized by UV irradiation for 24 h at 5 degreesC and further 3 h at 80 degreesC. The disulfide bonds of the resulting polymer were reductively cleaved by NaBH4 in methanol to give thiol groups in the binding sites. The polymer selectively recognized phenol rather than thiophenol. In chromatographic study using polymer-packed columns, the retention factor of the IP for phenol was 5.60 and that of a reference polymer was 4.20. The higher retention for phenol was supported by ab initio calculation. (C) 2002 Elsevier Science B.V. All rights reserved

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