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Infrared spectra of carbon monoxide-hydrogen sulfide van der Waals complexes in the C-O stretching region

机译:一氧化碳-硫化氢范德华配合物在C-O拉伸区的红外光谱

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The CO-stretching vibration-rotation spectra of CO-H2S, CO-D2S, and CO-HDS complexes have been studied in the 2150 cm(-1) region using a supersonic slit-jet expansion and a tunable diode laser spectrometer. The spectra were analyzed with the help of very recent microwave pure rotational studies of the same complexes. Two bands were assigned for each of the symmetric hydrogen sulfide isotopes, corresponding to the two nuclear spin modifications, para and ortho. The band origins were blue shifted, relative to the free CO molecule, by about 3.8 cm(-1) for CO-H2S and 4.3 cm(-1) for CO-D2S. These are considerably smaller shifts than exhibited by the related CO-water complexes, indicating that the intermolecular forces in CO-H2S are weaker and more isotropic. Crown Copyright (C) 2004 Published by Elsevier Inc. All rights reserved.
机译:使用超音速狭缝喷射扩展和可调二极管激光光谱仪研究了2150 cm(-1)区域中CO-H2S,CO-D2S和CO-HDS配合物的CO拉伸振动旋转光谱。借助最新的相同配合物的微波纯旋转研究对光谱进行了分析。为每个对称硫化氢同位素分配了两个谱带,分别对应于两个核自旋修饰(对位和邻位)。相对于游离的CO分子,谱带起源发生蓝移,CO-H2S约为3.8 cm(-1),CO-D2S约为4.3 cm(-1)。与相关的CO-水络合物相比,这些位移要小得多,这表明CO-H2S中的分子间作用力更弱且各向同性。 Crown版权所有(C)2004,由Elsevier Inc.出版。保留所有权利。

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