Stimulated emission pumping of intermolecular vibrations in OH–Ar(X 2Π)

Stimulated emission pumping of intermolecular vibrations in OH–Ar(X 2Π)
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OH–Ar(X 2Π) 中分子间振动的受激发射泵浦

DOI:
10.1063/1.462342
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发表时间:
1992
影响因子:
4.4
通讯作者:
M. Lester
M. Lester
中科院分区:
化学2区
文献类型:
--
作者:
Mary T. Berry;Richard A. Loomis;L. Giancarlo;M. Lester

文献摘要

被引文献

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受激发射光谱已被用于访问由OH(X 2Π)+Ar(1 S 0)势能面支持的分子间弯曲和拉伸振动。OH-Ar弯曲能级的流形与OH(2 <$3/2)的转动能级j=(3)/(2),(5)/(2)和(7)/(2)相关,分子间伸缩为0 ~ 3个量子。在与OH(2Π1/2)相关的自旋轨道激发态的分子间振动能级上也制备了OH-Ar配合物。第一个解离极限,产生OH(2 <$3/2)v=0,j=(3)/(2)+Ar(1 S 0)碎片,已被确定位于零点能级以上93至103 cm−1之间。在亚稳态水平制备的复合物,检测到超过第一解离极限200 cm−1,通过使用OH旋转或自旋轨道激发来破坏OH-Ar分子间键进行预解离。
Stimulated emission spectroscopy has been used to access the intermolecular bending and stretching vibrations supported by the OH(X 2Π)+Ar(1S0) potential‐energy surfaces. Manifolds of OH–Ar bending levels, correlating with the j= (3)/(2) , (5)/(2) , and (7)/(2) rotational levels of OH(2Π3/2), have been observed with zero to three quanta of intermolecular stretch. OH–Ar complexes have also been prepared in intermolecular vibrational levels of the spin–orbit excited state correlating with OH(2Π1/2). The first dissociation limit, producing OH(2Π3/2) v=0, j= (3)/(2) +Ar(1S0) fragments, has been determined to lie between 93 and 103 cm−1 above the zero‐point level. Complexes prepared in metastable levels, detected up to 200 cm−1 beyond the first dissociation limit, undergo predissociation by using OH rotational or spin–orbit excitation to break the OH–Ar intermolecular bond.