Long-range transition state theory

被引:252
作者
Georgievskii, Y [1 ]
Klippenstein, SJ [1 ]
机构
[1] Sandia Natl Labs, Combust Res Facil, Livermore, CA 94551 USA
基金
美国能源部;
关键词
D O I
10.1063/1.1899603
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 implementation of variational transition state theory (VTST) for long-range asymptotic potential forms is considered, with particular emphasis on the energy and total angular momentum resolved (mu J-VTST) implementation. A long-range transition state approximation yields a remarkably simple and universal description of the kinetics of reactions governed by long-range interactions. The resulting (mu J-VTST) implementation is shown to yield capture-rate coefficients that compare favorably with those from trajectory simulations (deviating by less than 10%) for a, wide variety of neutral and ionic long-range potential forms. Simple analytic results are derived for many of these cases. A brief comparison with a variety of low-temperature experimental studies illustrates the power of this approach as an analysis tool. The present VTST approach allows for a simple analysis of the applicability conditions for some related theoretical approaches. It also provides an estimate of the temperature or energy at which the "long-range transition state" moves to such short separations that short-range effects, such as chemical bonding, steric repulsion, and electronic state selectivity, must be considered. (c) 2005 American Institute of Physics.
引用
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页数:17
相关论文
共 68 条
[1]   ROLE OF ANGULAR-MOMENTUM IN STATISTICAL UNIMOLECULAR RATE THEORY [J].
AUBANEL, EE ;
WARDLAW, DM ;
ZHU, L ;
HASE, WL .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 1991, 10 (03) :249-286
[2]   MOLECULAR-MODELS FOR RECOMBINATION AND DISPROPORTIONATION OF RADICALS [J].
BENSON, SW .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1983, 61 (05) :881-887
[3]   Ultralow-temperature kinetics of CH(X(2)Pi) reactions: Rate coefficients for reactions with O-2 and NO (T=13-708 K), and with NH3 (T=23-295 K) [J].
Bocherel, P ;
Herbert, LB ;
Rowe, BR ;
Sims, IR ;
Smith, IWM ;
Travers, D .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (08) :3063-3069
[4]   Kinetics over a wide range of temperature (13-744 K): Rate constants for the reactions of CH(nu=0) with H-2 and D-2 and for the removal of CH(nu=1) by H-2 and D-2 [J].
Brownsword, RA ;
Canosa, A ;
Rowe, BR ;
Sims, IR ;
Smith, IWM ;
Stewart, DWA ;
Symonds, AC ;
Travers, D .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (18) :7662-7677
[5]   Low temperature rate coefficients for the reactions of CN and C2H radicals with allene (CH2=C=CH2) and methyl acetylene (CH3C≡CH) [J].
Carty, D ;
Le Page, V ;
Sims, IR ;
Smith, IWM .
CHEMICAL PHYSICS LETTERS, 2001, 344 (3-4) :310-316
[6]   ON STATISTICAL AND THERMODYNAMIC APPROACHES TO ION POLAR MOLECULE COLLISIONS [J].
CELLI, F ;
WEDDLE, G ;
RIDGE, DP .
JOURNAL OF CHEMICAL PHYSICS, 1980, 73 (02) :801-812
[7]   Neutral-neutral reactions at the temperatures sf interstellar clouds -: Rate coefficients for reactions of C2H radicals with O2, C2H2, C2H4 and C3H6 down to 15 K [J].
Chastaing, D ;
James, PL ;
Sims, IR ;
Smith, IWM .
FARADAY DISCUSSIONS, 1998, 109 :165-181
[8]   COLLISIONS IN A NON-CENTRAL FIELD - VARIATIONAL AND TRAJECTORY INVESTIGATION OF ION-DIPOLE CAPTURE [J].
CHESNAVICH, WJ ;
SU, T ;
BOWERS, MT .
JOURNAL OF CHEMICAL PHYSICS, 1980, 72 (04) :2641-2655
[9]  
CLARY DC, 1990, ANNU REV PHYS CHEM, V41, P61
[10]   RATES OF CHEMICAL-REACTIONS DOMINATED BY LONG-RANGE INTERMOLECULAR FORCES [J].
CLARY, DC .
MOLECULAR PHYSICS, 1984, 53 (01) :3-21