Collisional relaxation of vibrationally excited complex molecules following laser excitation: effect of supercollisions

1999 ◽  
Author(s):  
G. A. Zalesskaya ◽  
D. L. Yakovlev ◽  
E. G. Sambor ◽  
D. I. Baranovsky
1976 ◽  
Vol 54 (6) ◽  
pp. 943-948 ◽  
Author(s):  
Fa-Mei Wang ◽  
B. S. Rabinovitch

This paper describes an approach to the study of intramolecular energy relaxation of highly vibrationally excited complex molecules. The features of the decomposition of a series of chemically activated alkylcyclobutanes are outlined, including variable selectivity of the initial, non-randomized state of excitation. It is shown how this can afford both a qualitative test of the postulate of internal energy randomization employed in the Rice–Ramsperger–Kassel–Marcus treatment of unimolecular reactions, as well as a quantitative measure of the rate of relaxation. The study of the first members of this series, ethyl and dimethyl cyclobutane, is described. As expected, the first members can provide a lower limit to the relaxation rate, namely, λ > 1012 s−1.


1988 ◽  
Vol 124 (3) ◽  
pp. 359-369 ◽  
Author(s):  
Thomas G. Kreutz ◽  
Jack Gelfand ◽  
Richard B. Miles ◽  
Herschel Rabitz

2002 ◽  
Vol 117 (19) ◽  
pp. 8603-8606 ◽  
Author(s):  
Mathieu P. Schmid ◽  
Plinio Maroni ◽  
Rainer D. Beck ◽  
Thomas R. Rizzo

1966 ◽  
Vol 45 (6) ◽  
pp. 2322-2323 ◽  
Author(s):  
S. Penzes ◽  
O. P. Strausz ◽  
H. E. Gunning

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