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通过 CO/环氧化物的同步 ROCOP 和乙烯基单体的 RAFT 聚合一步法制备 CO 基嵌段共聚物。

A One-Step Route to CO -Based Block Copolymers by Simultaneous ROCOP of CO /Epoxides and RAFT Polymerization of Vinyl Monomers.

机构信息

School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.

Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, CAS, Changchun, 130022, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2018 Mar 26;57(14):3593-3597. doi: 10.1002/anie.201710734. Epub 2018 Feb 28.

Abstract

The one-step synthesis of well-defined CO -based diblock copolymers was achieved by simultaneous ring-opening copolymerization (ROCOP) of CO /epoxides and RAFT polymerization of vinyl monomers using a trithiocarbonate compound bearing a carboxylic group (TTC-COOH) as the bifunctional chain transfer agent (CTA). The double chain-transfer effect allows for independent and precise control over the molecular weight of the two blocks and ensures narrow polydispersities of the resultant block copolymers (1.09-1.14). Notably, an unusual axial group exchange reaction between the aluminum porphyrin catalyst and TTC-COOH impedes the formation of homopolycarbonates. By taking advantage of the RAFT technique, it is able to meet the stringent demand for functionality control to well expand the application scopes of CO -based polycarbonates.

摘要

通过使用带有羧酸基团的三硫代碳酸酯化合物(TTC-COOH)作为双官能团链转移剂(CTA),同时进行 CO/环氧化物的开环共聚(ROCOP)和乙烯基单体的 RAFT 聚合,实现了具有明确结构的 CO 基两嵌段共聚物的一步合成。双链转移效应允许对两个嵌段的分子量进行独立和精确的控制,并确保所得嵌段共聚物具有较窄的多分散性(1.09-1.14)。值得注意的是,铝卟啉催化剂和 TTC-COOH 之间的异常轴向基团交换反应阻碍了均聚碳酸酯的形成。通过利用 RAFT 技术,能够满足对功能控制的严格要求,从而很好地扩展了 CO 基聚碳酸酯的应用范围。

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