共 50 条
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
来源:
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.
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页码:23 / 30
页数:8
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