MOLECULAR-BEAM STUDIES OF THE PHOTODISSOCIATION OF BENZENE AT 193 AND 248 NM

被引:105
作者
YOKOYAMA, A
ZHAO, X
HINTSA, EJ
CONTINETTI, RE
LEE, YT
机构
[1] UNIV CALIF BERKELEY LAWRENCE BERKELEY LAB,DIV MAT & CHEM SCI,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,DEPT CHEM,BERKELEY,CA 94720
关键词
D O I
10.1063/1.457780
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 photodissociation processes of benzene following excitation at 193 and 248 nm have been studied by molecular beam photofragmentation translational spectroscopy. When benzene was excited to the 1B1u state by absorption at 193 nm, dissociation occurred through three primary channels, C6H5 + H (80%), C6H4 + H2 (16%), and C5H3 + CH3 (4%), following internal conversion to the vibrationally excited ground state. When benzene was excited to the 1B2u state at 248 nm, two primary dissociation channels, C6H4 + H2 (96%), and C 5H3 + CH3 (4%), were observed. Photodissociation to produce two C3H3 was induced by two photon absorption of benzene at both 193 and 248 nm. Numerous secondary photodissociation processes of the primary photoproducts were also observed at both 193 and 248 nm. © 1990 American Institute of Physics.
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页码:4222 / 4233
页数:12
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