Some key factors of energy distributions in the products of complex-forming elementary reactions

被引:39
作者
Bonnet, L [1 ]
Rayez, JC
机构
[1] Univ Bordeaux 1, Lab Physicochim Mol, UMR 5803, F-33405 Talence, France
[2] CNRS, F-33405 Talence, France
关键词
D O I
10.1039/a809986c
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
We review some conceptual and technical tools that help in the understanding of the global shape of energy distributions in the products of complex-forming three-atom reactions governed by long-range forces. The phase space theory (PST) of chemical reactions is simplified so as to arrive at an analytical expression of the recoil energy distribution in which two major factors of the dynamics appear explicitly. These factors are called the angular excitation rho(1)' and the diatomic inertial contribution rho(2)' for physical reasons that are detailed in the paper. In the case of strong angular excitations, a third quantity is shown to play a role, namely, the total angular momentum dependence of the reaction probability. We also propose a straightforward procedure for estimating the statistical energy partitioning in the context of the previous findings. In this regard, the procedure should help the experimentalist significantly in the search for some of the physical factors influencing his results.
引用
收藏
页码:2383 / 2400
页数:18
相关论文
共 149 条
[101]   ENERGY-DEPENDENCE OF THE CHEMI-LUMINESCENT BA(6S5DD-1(2)+O-2-]BAOSTAR+O REACTION [J].
MESTDAGH, JM ;
MEYNADIER, P ;
DEPUJO, P ;
SUBLEMONTIER, O ;
VISTICOT, JP ;
ALCARAZ, C ;
BERLANDE, J ;
CUVELLIER, J .
CHEMICAL PHYSICS LETTERS, 1989, 164 (01) :5-11
[103]   COLLISION DYNAMICS AND THE THERMAL RATE COEFFICIENT FOR THE REACTION H+O2-]OH+O [J].
MILLER, JA .
JOURNAL OF CHEMICAL PHYSICS, 1981, 74 (09) :5120-5132
[104]  
MILLER WB, 1967, DISCUSS FARADAY SOC, P108, DOI 10.1039/df9674400108
[105]   TUNNELING AND STATE SPECIFICITY IN UNIMOLECULAR REACTIONS [J].
MILLER, WH .
CHEMICAL REVIEWS, 1987, 87 (01) :19-27
[106]   QUASI-CLASSICAL TRAJECTORY STUDY OF THE LI+CS-2 REACTION [J].
MORAIS, VMF ;
VARANDAS, AJC .
MOLECULAR PHYSICS, 1995, 84 (05) :957-969
[107]   DYNAMICS OF THE LI+LI-2-]LI-2+LI ISOERGIC EXCHANGE-REACTION - A COMPARATIVE-STUDY ON 2 POTENTIAL-ENERGY SURFACES [J].
MORAIS, VMF ;
VARANDAS, AJC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1989, 85 :1-10
[108]   ARE THE REACTIONS LI+NA2 AND NA+K2 DIRECT OR INDIRECT - A DYNAMICS STUDY OF SEMIEMPIRICAL VALENCE-BOND POTENTIAL-ENERGY SURFACES [J].
MORAIS, VMF ;
VARANDAS, AJC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1987, 83 :2247-2260
[109]   Nonstatistical unimolecular dissociation over a barrier [J].
Mordaunt, DH ;
Osborn, DL ;
Neumark, DM .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (06) :2448-2457
[110]   CLASSICAL DYNAMICS OF THE REACTION OF S(3P) WITH O2(3-SIGMA-G-) [J].
MURRELL, JN ;
CRAVEN, W ;
FARANTOS, SC .
MOLECULAR PHYSICS, 1983, 49 (05) :1077-1084