Structure-reactivity relationships in radical reactions: A novel method for the simultaneous determination of absolute rate constants and structural features

被引:58
作者
Gatlik, I
Rzadek, P
Gescheidt, G
Rist, G
Hellrung, B
Wirz, J
Dietliker, K
Hug, G
Kunz, M
Wolf, JP
机构
[1] Univ Basel, Inst Phys Chem, CH-4056 Basel, Switzerland
[2] Ciba Specialty Chem Inc, Addit, CH-4002 Basel, Switzerland
关键词
D O I
10.1021/ja991008f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Analysis of the ESR line width in time-resolved (TR-ESR) experiments is shown to be a suitable tool for the measurement of addition constants of phosphinoyl and substituted benzoyl radicals. Compared with kinetic investigations, which make use of the resonance intensity or integral, observation of the line width as a function of monomer concentration has the advantage that the experimental parameter is not affected by spin-polarization processes and, therefore, a lengthy determination of these polarization parameters is avoided. The resulting addition constants are discussed with respect to the experimental hyperfine coupling constants and the geometry of the radicals. TR-ESR experiments simultaneously provide rate constants and ESR parameters and allow structure-reactivity relationships to be established.
引用
收藏
页码:8332 / 8336
页数:5
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