Nitroxide-Mediated Polymerization of 2-Hydroxyethyl Methacrylate (HEMA) Controlled with Low Concentrations of Acrylonitrile and Styrene

被引:5
|
作者
Mei, Wenwen [1 ]
Maric, Milan [1 ]
机构
[1] McGill Univ, 3610 Univ St, Montreal, PQ H3A 0C5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
2-hydroxyethyl methacrylate; copolymerization; nitroxide-mediated polymerization; FREE-RADICAL POLYMERIZATION; AMPHIPHILIC BLOCK-COPOLYMERS; O-BOND HOMOLYSIS; METHYL-METHACRYLATE; SUCCINIMIDYL-ESTER; STATISTICAL COPOLYMERS; PROPAGATION KINETICS; DIBLOCK COPOLYMERS; MODEL ALKOXYAMINES; SIDE-CHAINS;
D O I
10.1002/mren.201600067
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nitroxide-mediated controlled radical polymerization of 2-hydroxyethyl methacrylate (HEMA) is achieved using the copolymerization method with a small initial concentration of acrylonitrile (AN, 5-16 mol%)) or styrene (S, 5-10 mol%). The polymerization is mediated by N-tert-butyl-N-(1-diethyl phosphono-2,2-dimethyl propyl) nitroxide (SG1)-based BlocBuilder unimolecular alkoxyamine initiator modified with an N-succinimidyl ester group (N-hydroxysuccinimide-BlocBuilder). As little as 5% molar feed of acrylonitrile results in a controlled polymerization, as evidenced by a linear increase in number average molecular weight Mn with conversion and dispersities (D) as low as 1.30 at 80% conversion in N, N-dimethylformamide (DMF) at 85 degrees C. With S as the controlling comonomer, higher initial S composition (approximate to 10 mol%) is required to maintain the controlled copolymerization. Poly(HEMA-ran-AN) s with Mn ranging from 5 to 20 kg mol(-1) are efficiently chain extended using n-butyl methacrylate/styrene mixtures at 90.0 degrees C in DMF, thereby showing a route to HEMAbased amphiphilic block copolymers via nitroxide-mediated polymerization.
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页数:13
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