Star-polymer synthesis via radical reversible addition-fragmentation chain-transfer polymerization

被引:207
作者
Stenzel-Rosenbaum, M [1 ]
Davis, TP [1 ]
Chen, V [1 ]
Fane, AG [1 ]
机构
[1] Univ New S Wales, Ctr Adv Macromol Design, Sch Chem Engn & Ind Chem, Sydney, NSW 2052, Australia
关键词
polystyrene stars; RAFT; living radical; termination;
D O I
10.1002/pola.1256
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polystyrene stars were synthesized by reversible addition-fragmentation chain-transfer (RAFT) polymerization using hexakis(thiobenzoylthiomethyl)benzene (I) as a hexafunctional RAFT agent at 80, 100, and 120 degreesC. The polymerizations conformed to pseudo-first-order kinetic behavior. TI-ie molecular weight distributions displayed characteristics consistent with a living radical process. A number of salient features were observed in the molecular weight distributions with the star distribution accompanied by a linear polymer-chain distribution and shoulders on the distributions that can be attributed to radical-radical-termination events. The evidence suggests that high temperatures are required to activate all the RAFT active sites on I, and a hypothesis proposes that there is significant steric hindrance in the initial stages of the RAFT process with I. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:2777 / 2783
页数:7
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