负离子光脱离作为双分子过渡态的探针:F + H2反应

A. Weaver, D. Neumark
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引用次数: 47

摘要

利用负离子FH-2、FD-2和FDH -的光电子能谱研究了F + H2、F + D2和F + HD反应的过渡态区。这些阴离子的光剥离可以进入中性的三个电子态,但通过调节光剥离激光器的偏振可以选择性地观察到反应向基态势能表面的跃迁。在这些条件下,FH-2光谱与Zhang和Miller最近使用T5a势能面模拟F + H2反应的结果相似。所有三种同位素阴离子的光谱都是通过与先前的反应散射计算的比较来解释的。这一比较强烈地表明,光电子能谱中的几个峰是由于向散射共振的转变而产生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Negative-ion photodetachment as a probe of bimolecular transition states: the F + H2 reaction
The transition-state region of the F + H2, F + D2 and F + HD reactions has been studied by photoelectron spectroscopy of the negative ions FH–2, FD–2 and FDH–. Photodetachment of these anions can access three electronic states of the neutral, but transitions to the ground-state potential-energy surface for the reaction can be observed selectively by adjusting the polarization of the photodetachment laser. Under these conditions, the FH–2 spectrum is similar to the recent simulation by Zhang and Miller which used the T5a potential-energy surface for the F + H2 reaction. The spectra of all three isotopic anions are interpreted by comparison to previous reactive scattering calculations. This comparison strongly suggests that several of the peaks in the photoelectron spectra are due to transitions to scattering resonances.
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