Matrix Isolation and Computational Study on the Photolysis of CHCl2COCl

Nobuaki Tanaka
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引用次数: 4

Abstract

UV light photolysis of dichloroacetyl chloride (CHCl2COCl) has been investigated by infrared spectroscopy in cryogenic Ar, Kr, Xe, and O2 matrices. The formation of CHCl3 and CO was found to be the dominant process over the ketene formation. The C-C bond cleaved products CHCl2 and COCl were also observed. As the number of the chlorine atom substitution to methyl group of acetyl chloride increased, the C-C bond cleaved product yield in the triplet state increased, which can be attributed to an internal heavy-atom effect where the intersystem crossing rate was enhanced.
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CHCl2COCl光解的基质分离与计算研究
用红外光谱法研究了低温氩、氪、氙和氧基质中紫外光解二氯乙酰氯(CHCl2COCl)的反应。CHCl3和CO的形成是酮烯形成的主要过程。C-C键裂解产物CHCl2和COCl也被观察到。随着氯原子取代到乙酰氯甲基的次数增加,三态C-C键裂解产物的产率增加,这可归因于内部重原子效应,系统间的交叉速率增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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