CLASSICAL PHASE-SPACE THEORY FOR PRODUCT STATE DISTRIBUTIONS WITH APPLICATION TO THE V-J VECTOR CORRELATION

被引:52
作者
KLIPPENSTEIN, SJ
CLINE, JI
机构
[1] UNIV NEVADA,DEPT CHEM,RENO,NV 89557
[2] UNIV NEVADA,CHEM PHYS PROGRAM,RENO,NV 89557
关键词
D O I
10.1063/1.470529
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
A classical phase space theory procedure for estimating product state distributions for ''barrierless'' dissociations is described. The distributions are determined in terms of an average over the available phase-space on a fixed dividing surface of the function describing the distribution of interest. The use of a weighting function corresponding to the contribution of each randomly sampled phase space point to the number of available states, as in related state counting algorithms, provides an efficient route to the determination of any particular product state distribution of correlation. The coordinates employed in this sampling are the Euler angles, describing the orientation in space of each of the fragments and of the line of centers connecting the two fragments, and their conjugate momenta. Sample applications focus on the determination of the vector correlation between the angular momentum of one fragment and the relative velocity of the fragments for the dissociations of 2-chloro-2-nitrosopropane (CNP), NCCN, and CF3NO. Comparisons with the corresponding experimental measurements for the CNP and NCCN dissociations provide further evidence for the presence of important dynamical effects in these dissociations. The calculations for CF3NO are presented with the hope of motivating an experimental verification of the predicted strong v-j correlation for the CF3 fragment in combination with the weak correlation for the NO fragment. Overall, these phase space theory results are found to provide a useful reference for the interpretation of experimental results. (C) 1995 American Institute of Physics.
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页码:5451 / 5460
页数:10
相关论文
共 58 条
[1]  
[Anonymous], 1986, AB INITIO MOL ORBITA
[2]   VECTOR CORRELATIONS IN MOLECULAR PHOTODISSOCIATION - H2O2, HONO2 AND (CH3)3COOH [J].
AUGUST, J ;
BROUARD, M ;
DOCKER, MP ;
HODGSON, A ;
MILNE, CJ ;
SIMONS, JP .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1988, 92 (03) :264-273
[3]   CALCULATED POTENTIAL-ENERGY SURFACES FOR THE ELECTRONIC STATES OF NCNO THAT DISSOCIATE TO THE PRODUCTS CN(X2-SIGMAT)+NO(X2II) [J].
BAI, YY ;
SEGAL, GA .
CHEMICAL PHYSICS LETTERS, 1988, 151 (1-2) :31-34
[4]   ROTATIONALLY MEDIATED VECTOR CORRELATIONS IN THE PHOTODISSOCIATION OF H2O (1,0,0) [J].
BAR, I ;
DAVID, D ;
ROSENWAKS, S .
CHEMICAL PHYSICS, 1994, 187 (1-2) :21-33
[5]  
BOWER RD, 1983, J CHEM PHYS, V79, P2798
[6]  
BRUHLMANN U, 1987, J CHEM PHYS, V86, P1249, DOI 10.1063/1.452214
[7]   STATE-TO-STATE PHOTODISSOCIATION DYNAMICS OF TRANS-GLYOXAL [J].
BURAK, I ;
HEPBURN, JW ;
SIVAKUMAR, N ;
HALL, GE ;
CHAWLA, G ;
HOUSTON, PL .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (03) :1258-1268
[8]   PHOTODISSOCIATION DYNAMICS OF FORMALDEHYDE - H-2 (V,J) VECTOR CORRELATIONS [J].
CARLETON, KL ;
BUTENHOFF, TJ ;
MOORE, CB .
JOURNAL OF CHEMICAL PHYSICS, 1990, 93 (06) :3907-3918
[9]   STATISTICAL PHASE SPACE THEORY OF POLYATOMIC SYSTEMS - RIGOROUS ENERGY AND ANGULAR-MOMENTUM CONSERVATION IN REACTIONS INVOLVING SYMMETRIC POLYATOMIC SPECIES [J].
CHESNAVICH, WJ ;
BOWERS, MT .
JOURNAL OF CHEMICAL PHYSICS, 1977, 66 (06) :2306-2315
[10]   DYNAMICS OF MOLECULAR PHOTOFRAGMENTATION [J].
COMES, FJ ;
GERICKE, KH ;
GRUNEWALD, AU ;
KLEE, S .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1988, 92 (03) :273-281