Peroxyl radical clocks

被引:60
|
作者
Roschek, B
Tallman, KA
Rector, CL
Gillmore, JG
Pratt, DA
Punta, C
Porter, NA
机构
[1] Vanderbilt Univ, Dept Chem, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Ctr Mol Toxicol, Nashville, TN 37235 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2006年 / 71卷 / 09期
关键词
D O I
10.1021/jo0601462
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of peroxyl radical clocks has been developed and calibrated based on the competition between the unimolecular beta-fragmentation (k(beta)) of a peroxyl radical and its bimolecular reaction with a hydrogen atom donor (k(H)). These clocks are based on either methyl linoleate or allylbenzene and were calibrated directly with alpha-tocopherol or methyl linoleate, which have well-established rate constants for reaction with peroxyl radicals (k(H-tocopherol) = 3.5 x 10(6) M-1 s(-1), k(H-linoleate) = 62 M-1 s(-1)). This peroxyl radical clock methodology has been successfully applied to determine inhibition and propagation rate constants ranging from 10(0) to 10(7) M-1 s(-1).
引用
收藏
页码:3527 / 3532
页数:6
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