Issue 18, 2016

First double hydrophilic graft copolymer bearing a poly(2-hydroxylethyl acrylate) backbone synthesized by sequential RAFT polymerization and SET-LRP

Abstract

Two well-defined double hydrophilic graft copolymers comprising a hydrophilic poly(2-hydroxyethyl acrylate) (PHEA) backbone and hydrophilic poly(N-isopropylacrylamide) (PNIPAM) side chains were synthesized by the combination of reversible addition–fragmentation chain transfer (RAFT) polymerization, single-electron-transfer living radical polymerization (SET-LRP), and a grafting-from strategy. A 2-hydroxyethyl 2-((2-chloropropanoyloxy)methyl)acrylate monomer containing an SET-LRP initiating group (–OCOCH(CH3)Cl) was first RAFT homopolymerized to provide a PHEA-based homopolymer bearing a Cl-containing SET-LRP initiating group in every repeated unit with a narrow molecular weight distribution (Mw/Mn = 1.17). This homopolymer directly initiated SET-LRP of N-isopropylacrylamide at ambient temperature to afford the desired well-defined poly(2-hydroxyethyl acrylate)-graft-poly(N-isopropylacrylamide) graft copolymers (Mw/Mn ≤ 1.33) with hydroxyl in every repeated unit of the backbone without polymeric functionality transformation. The thermo-responsive phase behavior of the obtained double hydrophilic graft copolymers was investigated by UV/vis spectroscopy, 1H NMR, and dynamic light scattering (DLS).

Graphical abstract: First double hydrophilic graft copolymer bearing a poly(2-hydroxylethyl acrylate) backbone synthesized by sequential RAFT polymerization and SET-LRP

Supplementary files

Article information

Article type
Paper
Submitted
18 Mar 2016
Accepted
07 Apr 2016
First published
07 Apr 2016
This article is Open Access
Creative Commons BY license

Polym. Chem., 2016,7, 3156-3164

First double hydrophilic graft copolymer bearing a poly(2-hydroxylethyl acrylate) backbone synthesized by sequential RAFT polymerization and SET-LRP

Y. Cui, X. Jiang, C. Feng, G. Gu, J. Xu and X. Huang, Polym. Chem., 2016, 7, 3156 DOI: 10.1039/C6PY00489J

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