Flexible transition state theory for a variable reaction coordinate: Derivation of canonical and microcanonical forms with angular momentum conservation

被引:13
|
作者
Robertson, SH
Wardlaw, DM
Wagner, AF
机构
[1] Accelrys Inc, Cambridge CB4 0WN, England
[2] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
[3] Argonne Natl Lab, Argonne, IL 60439 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2002年 / 117卷 / 02期
关键词
D O I
10.1063/1.1480271
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
This paper extends work previously presented [J. Chem. Phys. 113, 2648 (2000)] to establish a rigorous expression for the angular momentum resolved microcanonical reactive flux. A kinetic energy expression in terms of the angular momentum, based on the coordinate system described in the above reference, is derived. Analytic integration over momenta conjugate to the coordinates that describe the relative orientation of the fragments is effected at the canonical level. The Laplace transform relation between canonical and microcanonical coefficients is then exploited to yield the angular momentum dependent microcanonical reactive flux. Evaluation of the resulting rate expression involves a numerical integral whose dimension, in most cases, is the same as the integrals in corresponding canonical and standard microcanonical forms. (C) 2002 American Institute of Physics.
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页码:593 / 605
页数:13
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