Lane Joseph R, Kjaergaard Henrik G, Plath Kathryn L, Vaida Veronica
Department of Chemistry, University of Otago, Dunedin, New Zealand.
J Phys Chem A. 2007 Jun 28;111(25):5434-40. doi: 10.1021/jp0688005. Epub 2007 Jun 2.
Vapor-phase OH-stretching overtone spectra of methanesulfonic acid and trifluoromethanesulfonic acid were recorded in the Deltav(OH) = 4 and 5 regions using cavity ring-down spectroscopy. We compare these spectra to those of sulfuric acid to consider the effect on vibrational overtone spectra of replacing one of the OH groups with a more or less electronegative group. We complement our experimental work with anharmonic oscillator local mode calculations of the OH-stretching frequencies and intensities. The presence of a weak intramolecular interaction between the hydrogen atom of the OH group and the oxygen atom of the adjacent S=O group in methanesulfonic acid lowers its OH-stretching frequency from what would otherwise be predicted based on the electronegativity of the methyl group.
使用光腔衰荡光谱法在Δv(OH) = 4和5区域记录了甲磺酸和三氟甲磺酸的气相OH伸缩倍频光谱。我们将这些光谱与硫酸的光谱进行比较,以考虑用一个电负性或多或少的基团取代其中一个OH基团对振动倍频光谱的影响。我们用OH伸缩频率和强度的非谐振子局域模式计算来补充我们的实验工作。甲磺酸中OH基团的氢原子与相邻S=O基团的氧原子之间存在弱分子内相互作用,这使其OH伸缩频率低于基于甲基电负性所预测的值。