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.
引用
收藏
页码:593 / 605
页数:13
相关论文
共 40 条
  • [21] Temperature dependence of rate coefficients and branching ratios for the NH2+NO reaction via microcanonical variational transition state theory
    Diau, EWG
    Smith, SC
    JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (30): : 12349 - 12354
  • [22] The separation of the reaction coordinate in transition state theory: Regularity and dimensionality reduction resulting from local symmetry
    Lorquet, J. C.
    JOURNAL OF CHEMICAL PHYSICS, 2019, 150 (16):
  • [23] Calculation of the transition state theory rate constant for a general reaction coordinate: Application to hydride transfer in an enzyme
    Watney, JB
    Soudackov, AV
    Wong, KF
    Hammes-Schiffer, S
    CHEMICAL PHYSICS LETTERS, 2006, 418 (1-3) : 268 - 271
  • [24] Quantized dynamical bottlenecks and transition state control of the reaction of D with H2:: Effect of varying the total angular momentum
    Chatfield, DC
    Mielke, SL
    Allison, TC
    Truhlar, DG
    JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (19): : 8387 - 8408
  • [25] Microcanonical transition state theory for activated gas-surface reaction dynamics:: Application to H2/Cu(111) with rotation as a spectator
    Abbott, Heather L.
    Harrison, Ian
    JOURNAL OF PHYSICAL CHEMISTRY A, 2007, 111 (39): : 9871 - 9883
  • [26] Canonical Variational Transition-State Theory Study of the CF3CHFCH2F + OH Reaction
    Gonzalez-Lafont, Angels
    Lluch, Jose M.
    Varela-Alvarez, Adrian
    Sordo, Jose A.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (08): : 2768 - 2777
  • [27] A RANDOM-MATRIX TRANSITION-STATE THEORY FOR THE PROBABILITY-DISTRIBUTION OF STATE-SPECIFIC UNIMOLECULAR DECAY-RATES - GENERALIZATION TO INCLUDE TOTAL ANGULAR-MOMENTUM CONSERVATION AND OTHER DYNAMICAL SYMMETRIES
    HERNANDEZ, R
    MILLER, WH
    MOORE, CB
    POLIK, WF
    JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (02): : 950 - 962
  • [28] Complex angular momentum theory of state-to-state integral cross sections: resonance effects in the F plus HD → HF(v′=3) + D reaction
    Sokolovski, D.
    Akhmatskaya, E.
    Echeverria-Arrondo, C.
    De Fazio, D.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2015, 17 (28) : 18577 - 18589
  • [29] Application of the canonical flexible transition state theory to CH3, CF3, and CCl3 recombination reactions
    Pesa, M
    Pilling, MJ
    Robertson, SH
    Wardlaw, DM
    JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (44): : 8526 - 8536
  • [30] Canonical variational transition-state theory study of the CF3CH2CH3+OH reaction
    Gonzalez-Lafont, Angels
    Lluch, Jose M.
    Varela-Alvarez, Adrian
    Sordo, Jose A.
    JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (02): : 328 - 335