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Issue 12, 2015
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Synthesis of well-defined α,ω-telechelic multiblock copolymers in aqueous medium: in situ generation of α,ω-diols

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Abstract

The synthesis of well-defined α,ω-dihydroxyl telechelic multiblock copolymers by sequential in situ chain extensions via aqueous Cu(0) mediated living radical polymerization (SET-LRP) is reported. The rapid disproportionation of Cu(I)Br in the presence of Me6-TREN in water has been exploited to generate Cu(0) and [Cu(II)Br2/Me6-TREN] in situ, resulting in rapid reaction rate and narrow molecular weight distributions. Under optimized conditions, a telechelic heptablock copolymer was obtained within 2 hours with a final dispersity of ∼1.1 while the monomer conversion was >99% for each block. A range of acrylamides and acrylates have been successfully incorporated within the same polymer backbone, including N-isopropylacrylamide (NIPAAm), N,N-diethylacrylamide (DEA) and N,N-dimethylacrylamide (DMA) and poly(ethylene glycol) methyl ether acrylate (PEGA480). The thermo-responsive nature of these materials was subsequently demonstrated via cloud point measurements as both a function of molecular weight and backbone functionality. In addition, the typically unwanted hydrolysis of the α- and ω-end groups in aqueous media was further exploited via isocyanate post-polymerization modifications to alter the end group functionality.

Graphical abstract: Synthesis of well-defined α,ω-telechelic multiblock copolymers in aqueous medium: in situ generation of α,ω-diols

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Submitted
29 Dec 2014
Accepted
15 Jan 2015
First published
16 Jan 2015

Polym. Chem., 2015,6, 2226-2233
Article type
Paper

Synthesis of well-defined α,ω-telechelic multiblock copolymers in aqueous medium: in situ generation of α,ω-diols

A. Simula, V. Nikolaou, A. Anastasaki, F. Alsubaie, G. Nurumbetov, P. Wilson, K. Kempe and D. M. Haddleton, Polym. Chem., 2015, 6, 2226
DOI: 10.1039/C4PY01802H

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