Integration of CuAAC Polymerization and Controlled Radical Polymerization into Electron Transfer Mediated "Click-Radical" Concurrent Polymerization

被引:17
|
作者
Xue, Wentao [1 ,2 ]
Wang, Jie [1 ,2 ]
Wen, Ming [1 ,2 ]
Chen, Gaojian [1 ,2 ]
Zhang, Weidong [1 ,2 ]
机构
[1] Soochow Univ, Ctr Soft Condensed Matter Phys & Interdisciplinar, Suzhou 215006, Peoples R China
[2] Soochow Univ, State & Local Joint Engn Lab Novel Funct Polymer, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
click-radical concurrent polymerization; controlled radical polymerization (CRP); CuAAC polymerization; electron transfer; one-pot; ALKYNE CYCLOADDITION CUAAC; ONE-POT REACTION; HYPERBRANCHED POLYMERS; RAFT POLYMERIZATION; BLOCK-COPOLYMERS; CHEMISTRY; ATRP; COMBINATION; FUNCTIONALIZATION; AZIDES;
D O I
10.1002/marc.201600733
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The successful chain-growth copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) polymerization employing Cu(0)/pentamethyldiethylenetriamine (PMDETA) and alkyl halide as catalyst is first investigated by a combination of nuclear magnetic resonance, gel-permeation chromatography, and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. In addition, the electron transfer mediated "click-radical" concurrent polymerization utilizing Cu(0)/PMDETA as catalyst is successfully employed to generate well-defined copolymers, where controlled CuAAC polymerization of clickable ester monomer is progressed in the main chain acting as the polymer backbone, the controlled radical polymerization (CRP) of acrylic monomer is carried out in the side chain. Furthermore, it is found that there is strong collaborative effect and compatibility between CRP and CuAAC poly-merization to improve the controllability.
引用
收藏
页数:6
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