化学
铈
钒
无机化学
光化学
氧化还原
异构化
碘化物
溴化物
电子转移
离子
卤化物
催化作用
有机化学
作者
Gábor Lente,József Kalmár,Zsuzsa Baranyai,Alíz Kun,Ildikó Kék,Dávid Bajusz,M. P. Takács,Lilla Veres,István Fábián
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2009-01-21
卷期号:48 (4): 1763-1773
被引量:235
摘要
The kinetics of the redox reactions of the peroxomonosulfate ion (HSO5−) with iron(II), vanadium(IV), cerium(III), chloride, bromide, and iodide ions were studied. Cerium(III) is only oxidized upon illumination by UV light and cerium(IV) is produced in a photoreaction with a quantum yield of 0.33 ± 0.03. Iron(II) and vanadium(IV) are most probably oxidized through one-electron transfer producing sulfate ion radicals as intermediates. The halide ions are oxidized in a formally two-electron process, which most likely includes oxygen-atom transfer. Comparison with literature data suggests that the activation entropies might be used as indicators distinguishing between heterolytic and homolytic cleavage of the peroxo bond in the redox reactions of HSO5−.
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