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The Extent Of Non-born-oppenheimer Coupling In The Reaction Of Ci(~2p) With Para-h_2

机译:Ci(〜2p)与对-h_2反应中非出生型奥本海默偶联的程度

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Elementary triatomic reactions offer a compelling test of our understanding of the extent of electron-nuclear coupling in chemical reactions, which is neglected in the widely applied Born-Oppenheimer (BO) approximation. The BO approximation predicts that in reactions between chlorine (Cl) atoms and molecular hydrogen, the excited spin-orbit state (Cl*) should not participate to a notable extent. We report molecular beam experiments, based on hydrogen-atom Rydberg tagging detection, that reveal only a minor role of Cl*. These results are in excellent agreement with fully quantum-reactive scattering calculations based on two sets of ab initio potential energy surfaces. This study resolves a previous disagreement between theory and experiment and confirms our ability to simulate accurately chemical reactions on multiple potential energy surfaces.
机译:基本的三原子反应为我们对化学反应中电子核耦合程度的理解提供了令人信服的测试,而在广泛应用的Born-Oppenheimer(BO)近似中却忽略了这一点。 BO近似值预测,在氯(Cl)原子与分子氢之间的反应中,受激自旋轨道状态(Cl *)不应显着参与。我们报告了基于氢原子Rydberg标签检测的分子束实验,该实验仅揭示了Cl *的微小作用。这些结果与基于两组从头算势能面的完全量子反应性散射计算非常吻合。这项研究解决了理论与实验之间的先前分歧,并确认了我们能够准确模拟多个势能面上的化学反应的能力。

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