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首页> 外文期刊>The Journal of Chemical Physics >Infrared absorption of gaseous ClCS detected with time-resolved Fourier-transform spectroscopy
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Infrared absorption of gaseous ClCS detected with time-resolved Fourier-transform spectroscopy

机译:时间分辨傅里叶变换光谱检测到的气态ClCS的红外吸收

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A transient infrared absorption spectrum of gaseous ClCS was detected with a step-scan Fourier-transform spectrometer coupled with a multipass absorption cell. ClCS was produced upon irradiating a flowing mixture of Cl2CS and N-2 or CO2 with a KrF excimer laser at 248 nm. A transient band in the region of 1160-1220 cm(-1), which diminished on prolonged reaction, is assigned to the C-S stretching (nu(1)) mode of ClCS. Calculations with density-functional theory (B3P86 and B3LYP/aug-cc-pVTZ) predict the geometry, vibrational wave numbers, and rotational parameters of ClCS. The rotational contour of the spectrum of ClCS simulated based on predicted rotational parameters agrees satisfactorily with experimental observation; from spectral simulation, the band origin is determined to be at 1194.4 cm(-1). Reaction kinetics involving ClCS, CS, and CS2 are discussed. (C) 2007 American Institute of Physics.
机译:气态ClCS的瞬态红外吸收光谱是通过与多程吸收池耦合的步进扫描傅立叶变换光谱仪检测的。用248 nm的KrF准分子激光辐照流动的Cl2CS和N-2或CO2的混合物后生成ClCS。瞬态带在1160-1220 cm(-1)的区域中,该区域在长时间的反应中会减小,它被分配给ClCS的C-S拉伸(nu(1))模式。利用密度泛函理论(B3P86和B3LYP / aug-cc-pVTZ)进行的计算可预测ClCS的几何形状,振动波数和旋转参数。根据预测的旋转参数模拟的ClCS光谱的旋转轮廓与实验观察结果令人满意;从光谱模拟中,确定带的起点为1194.4 cm(-1)。讨论了涉及ClCS,CS和CS2的反应动力学。 (C)2007美国物理研究所。

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