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首页> 外文期刊>Physical chemistry chemical physics: PCCP >Velocity-map ion-imaging of the NO fragment from the UV-photodissociation of nitrosobenzene
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Velocity-map ion-imaging of the NO fragment from the UV-photodissociation of nitrosobenzene

机译:亚硝基苯的紫外光解离生成NO片段的速度图离子成像

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摘要

The velocity and angular distribution of NO fragments produced by UV photodissociation of nitrosobenzene have been determined by velocity-map ion-imaging. Excitation of the S-2-state by irradiation into the peak of the first UV absorption band at 290.5 nm leads to a completely isotropic velocity distribution with Gaussian shape. The average kinetic energy in both fragments correlates with the rotational energy of the NO fragment and increases from 6% of the excess energy for j = 6.5 to 11% for j = 29.5. A similar isotropic distribution albeit with larger average velocity is observed when the ionization laser at 226 nm is also used for photodissociation, corresponding to excitation into a higher electronic state S-n (n greater than or equal to 3) of nitrosobenzene. It is concluded that photodissociation occurs on a timescale much slower than rotation of the parent molecule, and after redistribution of the excess energy into the vibrational degrees of freedom. [References: 57]
机译:通过速度图离子成像确定了亚硝基苯的紫外光解离所产生的NO片段的速度和角分布。通过辐照到290.5 nm处的第一个UV吸收带的峰中激发S-2-状态,导致具有高斯形状的完全各向同性的速度分布。两个片段中的平均动能与NO片段的旋转能相关,并且从j = 6.5的过剩能量的6%增加到j = 29.5的11%。当在226 nm处的电离激光也用于光离解时,观察到相似的各向同性分布,尽管平均速度较大,这对应于激发成亚硝基苯的更高电子态S-n(n大于或等于3)。结论是,光解离发生在比母体分子旋转慢得多的时间尺度上,并且在将多余的能量重新分配到振动自由度之后。 [参考:57]

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