Vibrational energy redistribution of ethanol oligomers and dissociation of hydrogen bonds after ultrafast infrared excitation

被引:41
作者
Laenen, R [1 ]
Rauscher, C [1 ]
Laubereau, A [1 ]
机构
[1] Tech Univ Munich, Dept Phys, D-85748 Garching, Germany
关键词
D O I
10.1016/S0009-2614(97)01301-8
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
2-color infrared spectroscopy of associated ethanol molecules is carried out viith subpicosecond time resolution in the solvent carbon tetrachloride (1.2 M) at room temperature. After excitation of the CH-vibration at 2974 cm(-1) rapid population redistribution with a time constant < 0.5 ps is observed within the CH-stretching region in agreement with earlier observations, while an effective population lifetime of 12 +/- 2 ps is measured. In addition, amazingly fast dissociation of H-bonds occurs, the dominant component of which is governed by a time constant of approximately 2 ps and proposed to be of thermal origin. Further spectral features are discussed, e.g. energy transfer between CH- and OH-vibrations. (C) 1998 Elsevier Science B.V.
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页码:7 / 14
页数:8
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