Issue 7, 2011

Azobenzene-containing molecularly imprinted polymer microspheres with photoresponsive template binding properties

Abstract

The first successful preparation of azobenzene (azo)-containing molecularly imprinted polymer (MIP) microspheres with photoresponsive template binding properties is described. A methacrylate azo functional monomer with a pyridine group was used for this purpose, and its good solubility in acetonitrile allowed the implementation of molecular imprinting viaprecipitation polymerization, leading to azo-containing MIP microspheres (number-average diameter = 1.33 μm, polydispersity index = 1.15) with obvious molecular imprinting effects towards the template 2,4-dichlorophenoxyacetic acid (2,4-D), rather fast template rebinding kinetics, and appreciable selectivity over structurally related compounds. The binding association constant Ka and apparent maximum number Nmax for high-affinity sites of the imprinted polymer in the dark environment were determined by Scatchard analysis to be 2.3 × 104 M−1 and 10.0 μmol g−1, respectively. Most importantly, the binding affinity of the imprinted sites in azo-containing MIP microspheres was found to be photoresponsive towards the template, which decreased upon UV light irradiation (as revealed by the resulting lower Ka value for high-affinity sites and reduced specific bindings), whereas it could be recovered during the subsequent thermal (or visible light-induced) back-isomerization. Furthermore, this photoregulation process proved to be highly repeatable under photoswitching conditions.

Graphical abstract: Azobenzene-containing molecularly imprinted polymer microspheres with photoresponsive template binding properties

Supplementary files

Article information

Article type
Paper
Submitted
01 Sep 2010
Accepted
01 Nov 2010
First published
17 Dec 2010

J. Mater. Chem., 2011,21, 2320-2329

Azobenzene-containing molecularly imprinted polymer microspheres with photoresponsive template binding properties

L. Fang, S. Chen, Y. Zhang and H. Zhang, J. Mater. Chem., 2011, 21, 2320 DOI: 10.1039/C0JM02898C

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