PICOSECOND REAL-TIME STUDIES OF MODE-SPECIFIC VIBRATIONAL PREDISSOCIATION

被引:70
作者
SEMMES, DH
BASKIN, JS
ZEWAIL, AH
机构
[1] Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena
关键词
D O I
10.1063/1.457847
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
The vibrational predissociation of several van der Waals complexes of t-stilbene has been studied by directly measuring, in real time, the fluorescence intensity from the initial reactant state and from the individual product states formed in the dissociation process after exciting single vibrational levels of the complex. With the aid of a kinetic model involving sequential processes, the individual rates for intramolecular vibrational redistribution and vibrational predissociation in the overall dissociation process are resolved and distinguished in several cases. In the stilbene-He complex, the dissociation is significantly faster from low energy out-of-plane modes than it is from a higher energy in-plane mode. © 1990 American Institute of Physics.
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页码:3359 / 3376
页数:18
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