Ultrafast intermolecular vibrational excitation transfer from solute to solvent: Observation of intermediate states

被引:22
作者
Son, Hyewon [1 ]
Park, Kwang-Hee [1 ]
Kwak, Kyung-Won [2 ]
Park, Sungnam [1 ,3 ]
Cho, Minhaeng [1 ,3 ]
机构
[1] Korea Univ, Dept Chem, Seoul 136713, South Korea
[2] Chung Ang Univ, Dept Chem, Seoul 156756, South Korea
[3] Korea Basic Sci Inst, Multidimens Spect Lab, Seoul 136713, South Korea
基金
新加坡国家研究基金会;
关键词
IR spectroscopy; Two-dimensional IR spectroscopy; Vibrational relaxation; Vibrational energy transfer; ENERGY TRANSFER; DYNAMICS; SPECTROSCOPY; PROBE; WATER;
D O I
10.1016/j.chemphys.2013.03.008
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
Ultrafast two-dimensional infrared (2DIR) and IR pump-probe (PP) spectroscopy was used to study the intermolecular vibrational energy transfer process from the excited state of asymmetric stretching vibration of HN3 to the overtone band of C-O stretching vibration of solvent methanol. A series of time-resolved 2DIR spectra indicate an intermolecular vibrational excitation transfer between the two modes, since the corresponding cross peaks appear at longer waiting times (>20 ps). However, detailed analyses of temperature-dependent FTIR, dispersed IR PP, and 2DIR spectra showed that the vibrational relaxation of the azido stretch mode and its energy transfer to solvent methanol C-O stretch overtone mode involve not only heat dissipation directly to the solvent bath modes but also production of transient intermediate states. The present experimental work demonstrates that ultrafast nonlinear IR spectroscopy is quite useful to shed light into the complicated vibrational relaxation dynamics of H-bonded solute-solvent systems. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:37 / 46
页数:10
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