The H+H2 reactive system.: Progress in the study of the dynamics of the simplest reaction

被引:114
作者
Aoiz, FJ [1 ]
Bañares, L
Herrero, VJ
机构
[1] Univ Complutense, Fac Quim, Dept Quim Fis, E-28040 Madrid, Spain
[2] CSIC, Inst Estructura Mat, E-28006 Madrid, Spain
关键词
D O I
10.1080/01442350500195659
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
Progress in the understanding of the H+H-2 reaction and its isotopic variants is reviewed with special attention to the achievements of the last decade. The detailed agreement between theory and experiment attained during this period is emphasized and major experimental and theoretical advances are highlighted. The excellent description of most experimental findings, from state-resolved cross sections to thermal rate constants, provided by the available quantum mechanical treatments, as well as the good overall behaviour of classical mechanics are underlined. Debated issues on short-lived complexes and delayed scattering, resonances and interferences, or geometric phase effects are extensively discussed. Finally, the state-of-the-art is summarized and prospects for future research on this prototypic system are presented.
引用
收藏
页码:119 / 190
页数:72
相关论文
共 234 条
[61]   GLOBAL CONTROL OF SUPRATHRESHOLD REACTIVITY BY QUANTIZED TRANSITION-STATES [J].
CHATFIELD, DC ;
FRIEDMAN, RS ;
TRUHLAR, DG ;
GARRETT, BC ;
SCHWENKE, DW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (02) :486-494
[62]   Quantized dynamical bottlenecks and transition state control of the reaction of D with H2:: Effect of varying the total angular momentum [J].
Chatfield, DC ;
Mielke, SL ;
Allison, TC ;
Truhlar, DG .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (19) :8387-8408
[63]   CONTROL OF CHEMICAL-REACTIVITY BY QUANTIZED TRANSITION-STATES [J].
CHATFIELD, DC ;
FRIEDMAN, RS ;
SCHWENKE, DW ;
TRUHLAR, DG .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (06) :2414-2421
[64]  
CHATFIELD DC, 1995, DYNAMICS MOL CHEM RE
[65]  
Child MS., 1974, MOL COLLISION THEORY
[66]   CROSSED MOLECULAR-BEAMS STUDY OF THE REACTION D+H-2-]DH+H AT COLLISION ENERGIES OF 0.53 AND 1.01 EV [J].
CONTINETTI, RE ;
BALKO, BA ;
LEE, YT .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (08) :5719-5740
[67]   RESONANCE STRUCTURE IN THE ENERGY-DEPENDENCE OF STATE-TO-STATE DIFFERENTIAL SCATTERING CROSS-SECTIONS FOR THE D+H2(V,J)-]HD(V',J')+H REACTION - COMMENT [J].
CONTINETTI, RE ;
ZHANG, JZH ;
MILLER, WH .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (07) :5356-5357
[68]   Interference of quantized transition-state pathways in the H+D2→D+HD chemical reaction [J].
Dai, DX ;
Wang, CC ;
Harich, SA ;
Wang, XY ;
Yang, XM ;
Chao, SD ;
Skodje, RT .
SCIENCE, 2003, 300 (5626) :1730-1734
[69]   A unified quantal and classical description of the stereodynamics of elementary chemical reactions:: State-resolved k-k'-j' vector correlation for the H+D2(v=0, j=0) reaction [J].
de Miranda, MP ;
Aoiz, FJ ;
Bañares, L ;
Rábanos, VS .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (12) :5368-5383
[70]   Using quantum rotational polarization moments to describe the stereodynamics of the H+D2(v=0,j=0)→HD(v′,j′)+D reaction [J].
de Miranda, MP ;
Clary, DC ;
Castillo, JF ;
Manolopoulos, DE .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (08) :3142-3153