光解
激发态
离解(化学)
光离子化
化学
氯
离子
氯化物
光化学
基态
原子物理学
物理化学
物理
电离
有机化学
作者
Christian T. Matthaei,D. Mukhopadhyay,Ingo Fischer
标识
DOI:10.1021/acs.jpca.0c11236
摘要
UV photodissociation of benzoyl chloride, Ph–CO–Cl, is associated with the loss of a chlorine atom. Here we excite benzoyl chloride to the S1, S2, and S3 excited states at 237, 253, 265, and 279.6 nm and detect the Cl photofragment by [1 + 1′] photoionization using 118.9 nm VUV radiation. The translational energy distribution of the Cl atom is measured by velocity map ion imaging. An isotropic image and a unimodal translational energy distribution are observed at all dissociation wavelengths, and a fraction of 18–20% of the excess energy is released into translation. The results indicate a dissociation that predominately proceeds from the vibrationally hot S0 ground state, although the observed translational energy release deviates significantly from a prior distribution. However, the impulsive model does also not represent the translational energy release. As a Cl/Cl* branching ratio of 9:1 or more is observed in one-color experiments at 235 nm, we conclude that direct dissociation from excited electronic states contributes only to a minor extent.
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