Macromolecular architectures based on organocatalytic ring-opening (co)polymerization of epoxides

被引:50
|
作者
Xia, Yening [1 ]
Zhao, Junpeng [1 ]
机构
[1] South China Univ Technol, Fac Mat Sci & Engn, 381 Wushan Rd, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer synthesis; Epoxide; Organocatalysis; Ring-opening polymerization; Copolymerization; GLYCIDYL PHENYL ETHER; N-BUTYLAMMONIUM FLUORIDE; ANIONIC ALTERNATING COPOLYMERIZATION; ACTIVATED MONOMER MECHANISM; CATIONIC VINYL-ADDITION; DEFINED POLY(PROPYLENE OXIDE); HIGH-MOLECULAR-WEIGHT; ONE-POT SYNTHESIS; ETHYLENE-OXIDE; BLOCK-COPOLYMERS;
D O I
10.1016/j.polymer.2018.03.047
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Epoxides are a major family of building materials for a variety of heterochain polymers that are of wide interests and great utilities in both academia and industry. Evolving the chemical tools for ring-opening (co)polymerization (ROP or ROCP) of epoxides and synthesis of epoxide-derived macromolecular structures have thus constituted a crucial part of synthetic polymer chemistry. Limitations can be broken and vigor be infused into this long-established field when it meets with the recently revived organocatalytic methods. In this feature article, the main organocatalytic systems applied to the ROP of epoxides are briefly described in terms of catalysts, mechanisms, and control over macromolecular characteristics. Then efforts made on diverse macromolecular architectures through epoxide-based organocatalytic (co)polymerization are specially summarized and discussed. Apart from synthesis of (co)polyether structures from ROP of epoxides, emphasis is also put on copolymer structures derived from epoxides and other types of compounds including vinyl monomers, cyclic esters, cyclic anhydrides, etc., through organocatalytic ROCP. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:343 / 361
页数:19
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