摩尔质量
聚合
双功能
环氧乙烷
开环聚合
化学
高分子化学
催化作用
链式转移
活性聚合
环氧乙烷
遥爪聚合物
共聚物
有机化学
“结束”组
聚合物
自由基聚合
作者
Chao Chen,Yves Gnanou,Xiaoshuang Feng
出处
期刊:Macromolecules
[American Chemical Society]
日期:2022-11-21
卷期号:55 (23): 10662-10669
被引量:16
标识
DOI:10.1021/acs.macromol.2c02078
摘要
The design of reactive species that can either serve to initiate the ring-opening polymerization of epoxides for the synthesis of high molar mass polyethers or be alternatively used to catalyze the synthesis of polyether telechelics in the presence of chain transfer agents has long been an elusive goal. Here, we report the synthesis of a series of bifunctional borinane-based catalysts that enable the living ring-opening polymerization of epoxides with an unprecedented activity (TOF ≥ 1.8 × 105 h–1) and a molar mass up to 106 g/mol under mild conditions. When used along with chain transfer agents to generate low Mn telechelics, the same borinane-based catalysts exhibit high productivity even for loading amounts as low as 50 ppb for ethylene oxide polymerization. These newly designed catalysts also afford the polymerization of oxetane with record TOF values and molar masses.
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