Stereospecific Living Radical Polymerization: Dual Control of Chain Length and Tacticity for Precision Polymer Synthesis

被引:267
作者
Satoh, Kotaro [1 ]
Kamigaito, Masami [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Nagoya, Aichi 4648603, Japan
基金
日本学术振兴会;
关键词
ASYMMETRIC INCLUSION POLYMERIZATION; RADIATION-INDUCED POLYMERIZATION; SYNDIOTACTIC POLY(VINYL ALCOHOL); POROUS COORDINATION POLYMERS; BOND-ASSISTED STEREOCONTROL; HANDED HELICAL CONFORMATION; ELECTRON-SPIN-RESONANCE; ISOTACTIC POLY(METHYL METHACRYLATE); CHIRAL RECOGNITION ABILITY; PHASE-TRANSITION BEHAVIOR;
D O I
10.1021/cr900115u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A review of the special issue of Chemical Review covers stereospecific living radical polymerizations for dual control of molecular weights and tacticity of the resulting polymers. These polymers have been achieved by combining controlled or living radical polymerization and stereospecific radical polymerization. It also treats fundamental aspects and the latest developments in each topic before discussing the simultaneous control in detail. It reveals most of the developed controlled and living radical polymerizations are based on the controlled formation of the growing radical species from the polymer terminus through reversible activation of the dormant species. Most of the polymer chain ends are in the dormant state, while a significantly small fraction of the dormant terminals are activated into the highly active growing radical species to allow an intermittent propagation during these polymerizations.
引用
收藏
页码:5120 / 5156
页数:37
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