Mechanism-Guided Design of Chain-Growth Click Polymerization Based on a Thiol-Michael Reaction

被引:12
|
作者
Jiang, Suqiu [1 ]
Huang, Hanchu [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Allylic Sulfide; Chain-Growth Polymerization; Click Polymerization; Ring-Opening Polymerization; Thiol-Michael Reaction; RING-OPENING POLYMERIZATION; STEP-GROWTH; PHOTOCAGED SUPERBASE; CONJUGATE ADDITION; POLYMERS; POLYSULFONES; CHEMISTRY; MONOMERS; TOOL;
D O I
10.1002/anie.202217895
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of chain-growth click polymerization is challenging yet desirable in modern polymer chemistry. In this work, we reported a novel chain-growth click polymerization based on the thiol-Michael reaction. This polymerization could be performed efficiently under ambient conditions and spatiotemporally regulated by ultraviolet light, allowing the synthesis of sulfur-containing polymers in excellent yields and high molecular weights. Density functional theory calculations indicated that the thiolate addition to the Michael acceptor is the rate-determining step, and introducing the phenyl group could facilitate the chain-growth process. This polymerization is a new type of chain-growth click polymerization, which will provide a unique approach to creating functional polymers.
引用
收藏
页数:7
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