CORIOLIS COUPLING IN AR-HCL

被引:12
|
作者
REEVE, SW
DVORAK, MA
FIRTH, DW
LEOPOLD, KR
机构
[1] Department of Chemistry, University of Minnesota, Minneapolis
基金
美国国家科学基金会;
关键词
D O I
10.1016/0009-2614(91)90364-F
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The PI-bending state of Ar-HCl has been examined by tunable far-infrared spectroscopy and the J dependence of the Coriolis coupling to the SIGMA-bending and SIGMA-stretching vibrations analyzed. The Coriolis coupling constants obtained are only slightly smaller than those previously observed in the complex containing a quantum of HCl of vibrational excitation (3.2% for the PI-SIGMA-bend coupling and 4.5% for the PI-SIGMA-stretch coupling). Deperturbed rotational constants determined for the SIGMA-bending state of the Cl-35 and Cl-37 species cannot be used in conjunction with simple moment of inertia expressions to support the predicted antihydrogen bonded geometry for that state. Comparisons between the ground states and the PI-states of the series Ar-HX (X = F, Cl, Br) are discussed.
引用
收藏
页码:259 / 266
页数:8
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