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Infrared spectra of OCS-C6H6, OCS-C6H6-He, and OCS-C6H6-Ne van der Waals complexes

机译:OCS-C6H6,OCS-C6H6-He和OCS-C6H6-Ne范德华配合物的红外光谱

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摘要

The infrared spectrum of weakly bound OCS\u2013C6H6 is studied in the region of the \u3bd1 fundamental band of OCS ( ~ 2050\u2002cm\u22121) using a tunable diode laser spectrometer to probe a pulsed supersonic jet expansion. This is one of the first direct infrared observations of a benzene-containing van der Waals complex. A very simple band is observed, corresponding to the parallel transition of a symmetric top. It is shifted by \u221211.1\u2002cm\u22121 with respect to the free OCS monomer. The isotopologues OCS\u201313C\u200912C5H6 and OC\u200934S\u2013C6H6 are observed, and the derived structure has OCS located along the benzene C6 symmetry axis in an S-bonded configuration with a center of mass separation of 4.42 \uc5, in good agreement with previous microwave spectra. Similar bands are observed for the trimers OCS\u2013C6H6\u2013He and OCS\u2013C6H6\u2013Ne, whose structure is obtained by adding an on-axis rare gas atom to the other side of the benzene. However, the analogous band for OCS\u2013C6H6\u2013Ar is not detected, raising the possibility that the stable form of this trimer may not have the same symmetrical structure. A \u201cmystery\u201d feature is observed close to the OCS\u2013C6H6 band origin and its possible assignment to a cluster such as OCS\u2013(C6H6)3 is discussed.
机译:使用可调谐二极管激光光谱仪在OCS基带(〜2050 \ u2002cm \ u22121)的区域中研究了弱束缚的OCS \ u2013C6H6的红外光谱,以探测脉冲超音速射流膨胀。这是含苯的范德华复合物的第一个直接红外观察结果。观察到一个非常简单的带,对应于对称顶部的平行过渡。相对于游离的OCS单体,它偏移了\ u221211.1 \ u2002cm \ u22121。观察到了同位素同位素OCS \ u201313C \ u200912C5H6和OC \ u200934S \ u2013C6H6,并且其衍生结构的OCS沿苯C6对称轴呈S键构型,质心分离度为4.42 \ uc5,与以前的微波光谱。对于三聚体OCS \ u2013C6H6 \ u2013He和OCS \ u2013C6H6 \ u2013Ne观察到相似的谱带,其结构是通过在苯的另一侧添加轴上稀有气体原子获得的。但是,未检测到OCS \ u2013C6H6 \ u2013Ar的类似谱带,这增加了此三聚体的稳定形式可能不具有相同对称结构的可能性。在靠近OCS \ u2013C6H6波段起点的地方观察到\ u201cmystery \ u201d特征,并讨论了其可能分配给诸如OCS \ u2013(C6H6)3之类的簇的情况。

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