STATE-RESOLVED PHOTODISSOCIATION OF N2O

被引:72
作者
HANISCO, TF [1 ]
KUMMEL, AC [1 ]
机构
[1] UNIV CALIF SAN DIEGO,DEPT CHEM,LA JOLLA,CA 92093
关键词
D O I
10.1021/j100130a020
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 of N2O at 203-205 nm has been investigated using state-resolved resonance-enhanced multiphoton ionization. The data are consistent with one-photon dissociation occurring via the bent 21A'(B1DELTA) excited state. The dissociation probability increases substantially over a nozzle temperature range 300-1500 K. The N2 fragment is highly rotationally excited as a result of the excited-state geometry. The rotational distribution of the N2 fragment is peaked at 1.4 eV and has a width of 0.6 eV. The average rotational energy of the N2 product is 1.4 +/- 0.1 eV; the average translational energy is 0.38 +/- 0.04 eV. There is no observed vibrational excitation in the N2 Product. The O(1D) product has an average translational energy of 0.67 +/-0.06 eV. The rotational energy of the products accounts for 57 +/- 4% and the translational energy accounts for 43 +/- 4% of the energy available to the products.
引用
收藏
页码:7242 / 7246
页数:5
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