Synthesis of graft copolymer with pendant macrocycles via combination of ATRP and click chemistry

被引:21
|
作者
Li, Min [1 ]
Liu, Chao [1 ]
Hong, Chun-Yan [1 ]
Pan, Cai-Yuan [1 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Cyclic polymer; Graft copolymer; Graft onto; GLASS-TRANSITION TEMPERATURE; CYCLIC POLYMERS; DIBLOCK COPOLYMERS; BLOCK-COPOLYMERS; WELL; RING; POLYMERIZATION; TOPOLOGIES; STAR; CONSTRUCTION;
D O I
10.1016/j.polymer.2015.06.046
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Graft copolymers with pendant macrocycles were synthesized via " graft onto" method. First, cyclic polystyrene (PS) was achieved by the combination of atom transfer radical polymerization (ATRP) and Cu-catalyzed azideealkyne cycloaddition (CuAAc), and then an alkynyl group was introduced to cyclic PS. Meanwhile, poly(3-azide-2-hydroxypropyl methacrylate) (PGMA-N-3) was synthesized by ATRP of glycidyl methacrylate (GMA) and successive ring-opening of pendant epoxide ring with NaN3. The graft copolymer was achieved by the following click reaction between PGMA-N-3 and alkynyl-containing cyclic PS. GPC and H-1 NMR were utilized to characterize the obtained graft copolymers, and a maximal grafting density of 20% was observed. Thermal behaviors of linear PS, cyclic PS and PGMA grafted with cyclic PS (PGMA-g-cPS) were investigated by differential scanning calorimeter (DSC), and T-g of PGMA-g-cPS is higher than those of linear and cyclic PS. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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