Chain-Growth Condensation Polymerization for Controlled Synthesis of Polymers

被引:10
|
作者
Ohta, Yoshihiro [1 ]
Yokozawa, Tsutomu [1 ]
机构
[1] Kanagawa Univ, Dept Mat & Life Chem, Kanagawa Ku, Yokohama, Kanagawa 2218686, Japan
关键词
Catalyst-transfer; Chain-growth condensation polymerization; Living polymerization; Polycondensation; pi-Conjugated polymers; CATALYST-TRANSFER POLYCONDENSATION; TRANSFER RADICAL POLYMERIZATION; CONTROLLED MOLECULAR-WEIGHT; BETA-(4-HYDROXYPHENYL) PROPIONIC-ACID; OPENING METATHESIS POLYMERIZATION; PREFERENTIAL OXIDATIVE ADDITION; CONJUGATED TRIBLOCK COPOLYMERS; CONDUCTING BLOCK-COPOLYMERS; WELL-DEFINED POLYTHIOPHENE; CROSS-COUPLING REACTIONS;
D O I
10.1007/12_2013_248
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Typical condensation polymerization is classified as a step-growth polymerization, in which the molecular weight of polymer obtained is difficult to control and the molecular weight distribution theoretically approaches 2 at high conversion. However, the mechanism of condensation polymerization of some monomers has been converted from step-growth to chain-growth by means of activation of the polymer end group by changing substituent effects between the monomer and the polymer, and activation of the polymer end group by intramolecular transfer to it of the catalyst. In this review, we describe the development of chain-growth condensation polymerization (CGCP) through the substituent effect and by catalyst transfer. Furthermore, construction of well-defined polymer architectures, such as block copolymers, star polymers, and graft copolymers by utilizing CGCP is also presented.
引用
收藏
页码:191 / 238
页数:48
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