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Synthesis of chiral amphiphilic diblock copolymers via consecutive RAFT polymerizations and their aggregation behavior in aqueous solution
Authors:Jian Wang  Wenliang Xu  Zhenping Cheng  Xiulin Zhu  Zhengbiao Zhang  Jian Zhu  Wei Zhang
Institution:1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow (Suzhou) University, Suzhou 215123, China;2. School Science of Jiangnan University, Wuxi 214000, China
Abstract:Two chiral amphiphilic diblock copolymers with different relative lengths of the hydrophobic and hydrophilic blocks, poly(6‐O‐p‐vinylbenzyl‐1,2:3,4‐Di‐O‐isopropylidene‐D ‐galactopyranose)‐b‐poly(N‐isopropylacrylamide) or poly(VBCPG)‐b‐poly(NIPAAM) and poly(20‐(hydroxymethyl)‐pregna‐1,4‐dien‐3‐one methacrylate)‐b‐poly(N‐isopropylacrylamide) or poly(MAC‐HPD)‐b‐poly(NIPAAM) were synthesized via consecutive reversible addition‐fragmentation chain‐transfer polymerizations of VBCPG or MAC‐HPD and NIPAAM. The chemical structures of these diblock copolymers were characterized by 1H nuclear magnetic resonance spectroscopy. These amphiphilic diblock copolymers could self‐assemble into micelles in aqueous solution, and the morphologies of micelles were investigated by transmission electron microscopy. By comparison with the lower critical solution temperatures (LCST) of poly(NIPAAM) homopolymer in deionized water (32 °C), a higher LCST of the chiral amphiphilic diblock copolymer (poly(VBCPG)‐b‐poly(NIPAAM)) was observed and the LCST increased with the relative length of the poly(VBCPG) block in the copolymer from 35 to 47 °C, respectively. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7690–7701, 2008
Keywords:amphiphilic copolymers  chiral  reversible addition‐fragmentation chain transfer (RAFT)  self‐assembly
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