Miller Benjamin J, Howard Daryl L, Lane Joseph R, Kjaergaard Henrik G, Dunn Meghan E, Vaida Veronica
Department of Chemistry, University of Otago, P.O. Box 56, Dunedin, New Zealand.
J Phys Chem A. 2009 Jul 2;113(26):7576-83. doi: 10.1021/jp9017162.
Vibrational spectra of vapor-phase ethanethiol and tert-butylthiol have been recorded in the 1000 to 12,000 cm(-1) region. Both the gauche and trans conformers of ethanethiol are observed. The intensities of SH-stretching vibrations are found to be significantly weaker than the equivalent CH-stretching vibrations and the OH-stretching vibrations in the corresponding alcohols. The relative strength of the SH-stretching vibrations in ethanethiol and tert-butylthiol compared with the OH-stretching vibrations in the corresponding alcohols are approximately 0.2 in the fundamental region and approximately 0.03 in the overtone regions. The SH- and OH-stretching intensities have been modeled with an anharmonic oscillator local mode model with ab initio calculated dipole moment functions. The weak nature of SH-stretching transitions is shown to be a result of both low anharmonicity of the vibrational mode and relatively small dipole moment derivatives.
已记录了气相乙硫醇和叔丁硫醇在1000至12000厘米⁻¹区域的振动光谱。观察到了乙硫醇的 gauche 和反式构象异构体。发现SH伸缩振动的强度明显弱于相应醇类中等效的CH伸缩振动和OH伸缩振动。在基频区域,乙硫醇和叔丁硫醇中SH伸缩振动与相应醇类中OH伸缩振动的相对强度约为0.2,在倍频区域约为0.03。利用具有从头算计算偶极矩函数的非谐振荡器局域模式模型对SH和OH伸缩强度进行了模拟。结果表明,SH伸缩跃迁的弱特性是振动模式的低非谐性和相对较小的偶极矩导数共同作用的结果。