McDonald D C, Wagner J P, McCoy A B, Duncan M A
Department of Chemistry , University of Georgia , Athens , Georgia 30602 , United States.
Department of Chemistry , University of Washington , Seattle , Washington 98195 , United States.
J Phys Chem Lett. 2018 Oct 4;9(19):5664-5671. doi: 10.1021/acs.jpclett.8b02499. Epub 2018 Sep 13.
Near-infrared spectroscopy measurements are presented for protonated water clusters, H(HO) , in the size range of n = 1-8. Clusters are produced in a pulsed-discharge supersonic expansion, mass selected, and studied with infrared laser photodissociation spectroscopy in the regions of 3600-4550 and 4850-7350 cm. Although there is some variation with cluster size, the main features of these spectra are a broad absorption near 5300 cm, a sharp doublet near 7200 cm, as well as a structured absorption near 4100 cm for n ≥ 2. The vibrational patterns measured for the hydronium, Zundel, and Eigen ions are compared to those predicted by different forms of anharmonic theory. Second-order vibrational perturbation theory (VPT2) and a local mode treatment of the OH stretches both capture key aspects of the spectra but suffer understandable deficiencies in the quantitative description of band positions and intensities.
本文给出了质子化水团簇H(HO)ₙ(n = 1 - 8)的近红外光谱测量结果。团簇通过脉冲放电超声速膨胀产生,进行质量选择,并在3600 - 4550 cm⁻¹和4850 - 7350 cm⁻¹区域用红外激光光解离光谱进行研究。尽管这些光谱的主要特征随团簇大小有一些变化,但主要特征是在5300 cm⁻¹附近有一个宽吸收峰,在7200 cm⁻¹附近有一个尖锐的双峰,以及对于n≥2在4100 cm⁻¹附近有一个结构化吸收峰。将测量得到的水合氢离子、曾德尔离子和艾根离子的振动模式与不同形式的非谐理论预测的模式进行了比较。二阶振动微扰理论(VPT2)和对OH伸缩振动的局域模式处理都捕捉到了光谱的关键特征,但在谱带位置和强度的定量描述方面存在一些可以理解的不足。