Photoionization/dissociation of alkyl substituted benzene molecules using intense near-infrared radiation

被引:69
作者
DeWitt, MJ [1 ]
Peters, DW [1 ]
Levis, RJ [1 ]
机构
[1] WAYNE STATE UNIV,DEPT CHEM,DETROIT,MI 48202
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0301-0104(97)00055-4
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 photoionization products for benzene, toluene, ethylbenzene and n-propylbenzene are measured using time-of-flight methods upon interaction with 780 nm radiation pulses of duration 170 fs and intensity 10(13-13.6) W cm(-2). The relative ionization yields scale as 1, 1.2, 1.4, and 0.35 for benzene, toluene, ethylbenzene and n-propylbenzene at maximum laser intensity. Limited dissociation was observed for benzene and toluene at all laser power densities. A significant (> 5%) dissociation/ionization yield was observed for ethylbenzene and n-propylbenzene at the lowest laser power densities. The dissociation increased as 11th order and 9th order processes for ethylbenzene and n-propylbenzene, respectively to a maximum of 70% dissociation/ionization for n-propylbenzene at 3.8 X 10(13) W cm(-2). At 3.8 X 10(13) W cm(-2) the dissociation yield increases quadratically with alkyl chain length for the series. The observed ionization/dissociation trends are consistent with a model which incorporates both Field ionization and energy redistribution concepts.
引用
收藏
页码:211 / 223
页数:13
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