PHOTODISSOCIATION DYNAMICS OF FORMALDEHYDE - H-2 (V,J) VECTOR CORRELATIONS

被引:44
作者
CARLETON, KL [1 ]
BUTENHOFF, TJ [1 ]
MOORE, CB [1 ]
机构
[1] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
关键词
D O I
10.1063/1.458777
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
Several bipolar moments of the H2 (υ,J) correlated angular momentum and velocity distribution produced from the photodissociation of formaldehyde near the threshold for dissociation have been measured by analysis of Doppler-resolved LIF line shapes. It is determined that the fragment H 2 (v·J) correlation is not at the limit of v⊥J, but is closer to the limit of v⊥J than to v∥ J. The rotation of the excited H2CO during the 10-7-10-8 s before dissociation does not completely wash out the lab-frame vector correlations. Anisotropy parameters as large as 0.85 and as small as -0.41 have been measured; these are outside the limits imposed by classical models of parent rotation. A quantum mechanical model for parent rotation is introduced that accounts for the large magnitude of the measured anisotropy parameters. Photolysis on the r R0(0) line of the 43 band produces fragments with β<0 while photolysis on the same rotational transition of the 2 141 band produces fragments with β> 0. It is not known if the different anisotropics are caused by differences in the parent transition dipole moment or by differences in the dissociation dynamics. The simple impulsive model that reproduces the fragment rotational distributions and product quantum-state correlations does not adequately describe the measured H2 (υ,J) vector correlations. © 1990 American Institute of Physics.
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页码:3907 / 3918
页数:12
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