硝化作用
苯酚
化学
光解
食腐动物
光化学
丙醇
动能
硝酸盐
溶剂
酒
重组
笼效应
无机化学
乙醇
有机化学
激进的
物理
基因
量子力学
生物化学
作者
Davide Vione,Babita Sur,Binay K. Dutta,Valter Maurino,Claudio Minero
标识
DOI:10.1016/j.jphotochem.2011.09.008
摘要
It is shown that the enhancement by 2-propanol of the nitration of phenol upon nitrate photolysis is compatible with the inhibition by the alcohol of in-cage recombination between O− and NO2. This effect would increase the availability of NO2 that is involved into phenol nitration, despite the enhancement by the alcohol of the production of superoxide that is a scavenger of NO2. A kinetic model is proposed to describe the experimental data and to get insight into the processes involved. Kinetic calculations suggest that in the absence of 2-propanol less than 25% of cage O− and NO2 would evolve into bulk species, the remainder undergoing recombination to nitrate. If reaction between cage O− and phenol were not negligible, the percentage of bulk species formation would be even lower. The data also show that most of the recombination between OH/O− and NO2 would take place in the solvent cage instead of the solution bulk.
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