Infrared spectroscopy of hydrated alkali metal cations: Evidence of multiple photon absorption

被引:24
作者
Beck, Jordan P. [1 ]
Lisy, James M. [1 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
美国国家科学基金会;
关键词
alkali metal compounds; hydrogen bonds; infrared spectra; molecule-photon collisions; multiphoton processes; photodissociation; photoexcitation; positive ions; predissociation; solvation; VIBRATIONAL PREDISSOCIATION SPECTROSCOPY; AB-INITIO CALCULATIONS; CLUSTER IONS; GAS-PHASE; MULTIPHOTON DISSOCIATION; WATER CLUSTERS; PHOTODISSOCIATION SPECTROSCOPY; EXCESS PROTON; SPECTRA; MOLECULES;
D O I
10.1063/1.3609760
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Infrared predissociation spectra of M+(H2O)(4-7), where M = alkali metal, are presented. Hydrogen bonding O-H stretching features are strongly dependent on which fragmentation channel is monitored. Spectra recorded by monitoring the loss of multiple waters show a preference for one absorption feature in the hydrogen-bonded region centered at similar to 3430-3500 cm(-1), which is assigned to linear-type hydrogen bonded OH stretches. Cyclic- and bent-type hydrogen bonded OH stretches have diminished photodissociation cross sections in the multiple ligand loss channels. Evidence from Rice-Ramsperger-Kassel-Marcus-evaporative ensemble calculations and laser fluence dependence experiments indicates that the multiple water loss channels are primarily the result of multiple photon absorption which we propose could be due to multiple, independent oscillators within a cluster ion each absorbing a photon during a single, 10 ns laser pulse. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3609760]
引用
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页数:6
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