Statistical quantum studies on insertion atom-diatom reactions

被引:107
作者
Gonzalez-Lezana, Tomas [1 ]
机构
[1] CSIC, Inst Matemat & Fis Fundamental, Serrano 123, E-28006 Madrid, Spain
关键词
D O I
10.1080/03081070600933476
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 study of insertion atom-diatom reactions is usually complicated by the existence of deep potential wells between reactants and products. The large number of hound and resonance states to be properly described makes exact quantum mechanical calculations extremely demanding in terms of numerical effort. In this type of collision, the process proceeds via the formation of an intermediate complex of finite lifetime. The application of statistical quantum methods provides a valid alternative to investigate the dynamics of the reaction. In this work. studies performed with a statistical quantum method recently developed by Rackham et al. on a variety of different reactions are extensively reviewed. The overall dynamics of the processes selected to test this statistical model range from complex-forming mechanisms to a competition between insertion and direct abstraction reaction pathways. This review includes studies Of X + H-2 reactions, where X is one of the following electronically excited non-metallic atoms: C(D-1), N(D-2). O(D-1) or S(D-1). An ion-diatom collision, the H-3(+) system (with its isotope variants), is also investigated. Finally, results of the statistical of the H + O-2 reaction are discussed. In all cases, comparison with both exact quantum mechanical calculations and experimental measurements shows that the method provides valid and rigorous information about the underlying dynamics of the reactions under study.
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页码:29 / 91
页数:63
相关论文
共 237 条
[1]   Dynamics of the H+O2 → O+OHchain-branching reaction:: Accurate quantum mechanical and experimental absolute reaction cross sections [J].
Abu Bajeh, M ;
Goldfield, EM ;
Nanf, A ;
Kappel, C ;
Meijer, AJHM ;
Volpp, HR ;
Wolfrum, J .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (13) :3359-3364
[2]   Global potential energy surfaces for the H+3 system.: Analytical representation of the adiabatic ground-state 1 1A′ potential [J].
Aguado, A ;
Roncero, O ;
Tablero, C ;
Sanz, C ;
Paniagua, M .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (03) :1240-1254
[3]   THE INITIAL PRODUCT VIBRATIONAL-ENERGY DISTRIBUTION IN THE REACTION BETWEEN O(1D2) AND H2 [J].
AKER, PM ;
SLOAN, JJ .
JOURNAL OF CHEMICAL PHYSICS, 1986, 85 (03) :1412-1417
[4]   Exploring the reaction dynamics of nitrogen atoms:: A combined crossed beam and theoretical study of N(2D)+D2→ND+D [J].
Alagia, M ;
Balucani, N ;
Cartechini, L ;
Casavecchia, P ;
Volpi, GG ;
Pederson, LA ;
Schatz, GC ;
Lendvay, G ;
Harding, LB ;
Hollebeek, T ;
Ho, TS ;
Rabitz, H .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (18) :8857-8860
[5]   Crossed molecular beams and quasiclassical trajectory studies of the reaction O(1D)+H2(D2) [J].
Alagia, M ;
Balucani, N ;
Cartechini, L ;
Casavecchia, P ;
van Kleef, EH ;
Volpi, GG ;
Kuntz, PJ ;
Sloan, JJ .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (16) :6698-6708
[6]   O(1D2)+H2→OH|v′≤4,N′⟩+H -: The anatomy of a reaction [J].
Alexander, AJ ;
Blunt, DA ;
Brouard, M ;
Simons, JP ;
Aoiz, FJ ;
Banares, L ;
Fujimura, Y ;
Tsubouchi, M .
FARADAY DISCUSSIONS, 1997, 108 :375-386
[7]   Product state-resolved stereodynamics: Quasiclassical study of the reaction O(D-1)+HD->OH(OD) (v', j')+D(H) [J].
Alexander, AJ ;
Aoiz, FJ ;
Brouard, M ;
Simons, JP .
CHEMICAL PHYSICS LETTERS, 1996, 256 (06) :561-568
[8]   Product multiplet branching in the O(1D)+H2→OH(2Π)+H reaction [J].
Alexander, MH ;
Rackham, EJ ;
Manolopoulos, DE .
JOURNAL OF CHEMICAL PHYSICS, 2004, 121 (11) :5221-5235
[9]   The plane wave packet approach to quantum scattering theory [J].
Althorpe, SC .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 2004, 23 (02) :219-251
[10]   Quantum scattering with energy-filtered plane wave packets: Visualizing the F+HD "ridge" mechanism [J].
Althorpe, SC .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (37) :7152-7160