真空紫外激光/飞行时间光谱法研究Cl2。

R. Lipson, S. Dimov, P. Wang, I. Okuda
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引用次数: 0

摘要

由于广泛的激发态扰动,Cl2的真空紫外(VUV)光谱非常不规则,过去很难解释1。这种情况在很大程度上被Peyerimhoff和Beunker2的从头计算所抵消。他们发现,在145 nm以下最强的VUV跃迁涉及第三层1∑u +离子对价态解离成Cl+(1Dg) + Cl-(1Sg),它与接近等能的4pp π 1∑u + Rydberg态相互作用,导致形成双阱势曲线,标记为1 1∑u +。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vacuum Ultraviolet Laser / Time-of-flight Spectroscopy of Cl2.
Vacuum ultraviolet (VUV) spectra of Cl2 are highly irregular due to extensive excited state perturbations, and in the past, have been difficult to interpret1. This situation was offset substantially by the ab initio calculations of Peyerimhoff and Beunker2. They showed that the strongest VUV transition below 145 nm involves a third tier 1 ∑ u + ion-pair valence state dissociating to Cl+(1Dg) + Cl-(1Sg), which interacts with the near isoenergetic 4pπ 1 ∑ u + Rydberg state leading to the formation of a double well potential curve, labelled 1 1 ∑ u + .
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