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Isolating the spectral signature of H3O+ in the smallest droplet of dissociated HCl acid

机译:在离解的HCl酸的最小液滴中分离H3O +的光谱特征

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摘要

The centrally important role of acids in aqueous chemistry has stimulated the search for the smallest droplet of hydrochloric acid. Based on several independent quantum calculations, this appears to be the HCl(H2O)(4) cluster, which dissociates into the so-called solvent ion pair (SIP), H3O+(H2O)(3)Cl-. Experimental verification of this prediction via infra-red spectroscopy is a major challenge and despite several recent reports of this SIP, there remains uncertainty about these observations. In this report, we present a calculation of the IR spectrum of the SIP in a fashion that isolates the contribution from the signature hydronium ion, H3O+. The computed spectrum indicates that the vibrational states of H3O+ are highly mixed, resulting in dispersed spectral features between 1300 and 3000 cm(-1), with the region between 2100 and 2900 cm(-1) being especially rich. These predictions point out the complexity of the SIP spectrum and offer guidelines for experiment. The energies of the HCl stretch fundamentals for three minima of the undissociated HCl(H2O)(4) cluster are also reported.
机译:酸在水性化学中的重要作用促使人们寻找最小的盐酸滴。根据几个独立的量子计算,这似乎是HCl(H2O)(4)团簇,它分解成所谓的溶剂离子对(SIP)H3O +(H2O)(3)Cl-。通过红外光谱对这一预测进行实验验证是一项重大挑战,尽管最近有几篇有关此SIP的报告,但有关这些观察仍存在不确定性。在此报告中,我们以一种将签名的水合氢离子H3O +的作用隔离开来的方式,对SIP的IR光谱进行了计算。计算出的光谱表明H3O +的振动状态高度混合,导致1300至3000 cm(-1)之间的分散光谱特征,其中2100至2900 cm(-1)之间的区域特别丰富。这些预测指出了SIP频谱的复杂性,并为实验提供了指导。还报告了三个未解离的HCl(H2O)(4)簇的最小值的HCl拉伸基本能的能量。

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