Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers

Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer...

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Veröffentlicht in:Macromolecules 2007-03, Vol.40 (5), p.1395-1400
Hauptverfasser: Southard, Glen E., Van Houten, Kelly A., Murray, George M.
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container_title Macromolecules
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creator Southard, Glen E.
Van Houten, Kelly A.
Murray, George M.
description Soluble molecularly imprinted polymers (MIPs) were prepared by reversible addition fragmentation chain transfer (RAFT) polymerization followed by ring-closing metathesis (RCM). The polymerization was done in the presence of a template to generate a processable star MIP. The core of the star polymer was a dithiobenzoate-substituted tris(β-diketonate)europium(III) complex. The tris(β-diketonate)europium(III) complex served as a polymerization substrate for the three-armed RAFT-mediated star polymer and as a luminescent binding site for dicrotophos, an organophosphonate pesticide. The star arms were AB block copolymers. Block A was either 1-but-3-enyl-4-vinylbenzene or a mixture of 1-but-3-enyl-4-vinylbenzene and styrene. Block B was styrene or methyl methacrylate. The but-3-enyls of block A were reacted by RCM with a second generation Grubbs catalyst to give an intramolecularly cross-linked core. The intramolecularly cross-linked MIP was soluble in common organic solvents. The 30% cross-linked soluble and processable star MIP was applied to the determination of dicrotophos with sub-ppb level detection limits.
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subjects Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Polymers with particular properties
Preparation, kinetics, thermodynamics, mechanism and catalysts
title Soluble and Processable Phosphonate Sensing Star Molecularly Imprinted Polymers
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