RAFT Copolymerization of Glycidyl Methacrylate and N,N-Dimethylaminoethyl Methacrylate

被引:9
|
作者
Cao Jun [1 ]
Zhang Lifen [1 ]
Pan Xiangqiang [1 ]
Cheng Zhenping [1 ]
Zhu Xiulin [1 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
reversible addition-fragmentation chain transfer; living radical polymerization; kinetics (polym; reactivity ratios; glycidyl methacrylate; N; N-dimethylaminoethyl methacrylate; FRAGMENTATION CHAIN TRANSFER; FREE-RADICAL POLYMERIZATION; REACTIVITY RATIOS; LINEAR METHODS; GENE DELIVERY; 2-(DIMETHYLAMINO)ETHYL METHACRYLATE; AMBIENT-TEMPERATURE; TRANSFECTION; POLYMERS; VECTORS;
D O I
10.1002/cjoc.201200625
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, copolymerization of two functional monomers, glycidyl methacrylate (GMA) and N,N-dimethylaminoethyl methacrylate (DMAEMA), was firstly carried out via reversible addition-fragmentation chain transfer (RAFT) polymerization successfully. The copolymerization kinetics was investigated under the molar ratio of n[GMA+DMAEMA]0/n[AIBN]0/n[CPDN]0=300/1/3 at 60 degrees C. The copolymerization showed typical "living" features such as first-order polymerization kinetics, linear increase of molecular weight with monomer conversion and narrow molecular weight distribution. The reactivity ratios of GMA and DMAEMA were calculated by the extended Kelen-Tudos linearization methods. The epoxy group of the copolymer PGMA-co-PDMAEMA remained intact under the conditions of RAFT copolymerization and could easily be post-modified by ethylenediamine. Moreover, the modified copolymer could be used as a gene carrier.
引用
收藏
页码:2138 / 2144
页数:7
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