首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Dependence of Calculated Product Rotational Polarizations on the Scattering Angle for the O(~1D) + HCl Reaction
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Dependence of Calculated Product Rotational Polarizations on the Scattering Angle for the O(~1D) + HCl Reaction

机译:O(〜1D)+ HCl反应的产物旋转极化对散射角的依赖性

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摘要

To investigate the effect of the structure of the potential energy surface on the vector properties of the O(~1D) + HCl reaction, we carried out a quasiclassical trajectory study of some two and three vector correlations. The analysis of the allocation of the angular momentum and of the variation with the scattering angle of the second Legendre moment related to the distribution of the product rotational angular momentum with respect to relative velocity indicated that the formation of an intermediate complex is responsible for deviations from the kinematic limiting behavior. The complex formation explains also the agreement of trajectory results with those of a statistical model reaction proposed by Herschbach (Case, D. A.; Herschbach, D. R. Mol. Phys. 1975, 30, 1537).
机译:为了研究势能表面的结构对O(〜1D)+ HCl反应的矢量性质的影响,我们对大约两个和三个矢量相关性进行了准经典轨迹研究。对角动量的分配以及第二勒让德矩的散射角随产品旋转角动量相对于相对速度的分布的变化的变化的分析表明,中间复合物的形成是导致与运动极限行为。络合物的形成还解释了轨迹结果与赫希巴赫提出的统计模型反应的轨迹的一致性(Case,D.A。; Herschbach,D.R.Mol.Phys.1975,30,1537)。

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