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Electronic Angular Momentum Polarizations of Atomic Fragments in Diatomic Photodissociations: Correlations between Electronic States in the Molecular and the Asymptotic Regions

机译:双原子光解离中原子片段的电子角动量极化:分子和渐近区中电子态之间的相关性

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摘要

To understand electronic angular momentum polarization phenomena of atomic photofragments in diatomic photodissociations, Wigner-Witmer correlation rules should be augmented to treat these problems quantitatively. The essential step to achieve this goal is to find the transformation relationships between basis functions of Hund's coupling cases (a) (or (b)) and (c). Because the partition of a united electronic configuration into two separated electronic configurations is undertaken, in general no analytical transformation can be established. To illustrate the present scheme in acquiring the transformation relationships, the direct photodissociation of O_2(B~3Σ_u~-)into O(~1D) + O(~3P) is explicitly considered. The electronic angular momentum polarization of oxygen atoms in|~1D, J=2, M_J=0> observed in the recent experiment on O_2 photodissociation can be rationalized by this quantitative correlation rule.
机译:要了解双原子光解离中原子光碎片的电子角动量极化现象,应增强Wigner-Witmer相关规则,以定量地解决这些问题。实现此目标的关键步骤是找到洪德耦合情况(a)(或(b))和(c)的基函数之间的转换关系。因为进行了将统一的电子配置分为两个单独的电子配置的操作,所以通常无法建立分析转换。为了说明本方案在获取转换关系中的方案,明确考虑了O_2(B〜3Σ_u〜-)直接光解为O(〜1D)+ O(〜3P)。通过该定量相关规则可以合理化在最近的O_2光解离实验中观察到的氧原子的电子角动量极化|| 1D,J = 2,M_J = 0>。

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