The reversible addition-fragmentation chain transfer process and the strength and limitations of modeling: Comment on "the magnitude of the fragmentation rate coefficient"

被引:151
作者
Barner-Kowollik, C [1 ]
Coote, ML
Davis, TP
Radom, L
Vana, P
机构
[1] Univ New S Wales, Sch Chem Engn & Ind Chem, Ctr Adv Macromol Design, Sydney, NSW 2052, Australia
[2] Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia
[3] Univ Gottingen, Inst Chem Phys, D-37077 Gottingen, Germany
关键词
living free-radical polymerization; kinetics (polym.); reversible addition-fragmentation chain transfer (RAFT); modeling; quantum chemistry;
D O I
10.1002/pola.10854
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
There is appreciable uncertainty concerning the magnitude of the fragmentation rate coefficient of the intermediate radical in reversible addition-fragmentation chain transfer (RAFT) polymerizations. A large proportion of the experimental and theoretical evidence suggests that it is a stable species with a lifetime longer than 0.0001 s. This is particularly the case when the intermediate macro-RAFT radical is stabilized by a phenyl group attached to the radical center or has a poor leaving group. Although the occurrence to some extent of irreversible termination reactions cannot be excluded, we argue that such reactions are more likely to be a result of slow fragmentation of the intermediate macro-RAFT radical. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:2828 / 2832
页数:5
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