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Title: Internal energy distributions from nitrogen dioxide fluorescence. 3. Photolysis of jet-cooled N[sub 2]O[sub 4]

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100141a006· OSTI ID:5525888
; ;  [1]
  1. Univ. of California, Berkeley, CA (United States) Lawrence Berkeley Lab., CA (United States)

A supersonic jet of N[sub 2]O[sub 4] is photolyzed at three wavelengths: 351, 248, and 193 nm. The resultant NO[sub 2] fluorescence is dispersed, the fluorescence spectrum is folded into a cumulative sum, and the internal energy distribution of almost nascent photolysis products is found by the method of article 1 of this series. The spread of these product internal energy distributions increases as the photolysis energy increases from 351 to 248 to 193 nm. The most probable internal energy increases between 351- and 248-nm photolysis, but at 193-nm photolysis it is about the same as, or somewhat lower than, that at 248 nm. This apparent anomaly is explained in terms of the electronic states of the products. The internal energy distribution derived from 351-nm data is examined by the method of prior distribution, and the photolysis products are found to be one NO[sub 2] molecule in the ground electronic state and the other in the [sup 2]B[sub t] electronic state with 3 or 4 quanta of bending vibration excitation. The internal energy distributions at 193 and 248 nm are combined with Kawasaki's time-of-flight translational energy distributions at 193 and 248 nm, and upon adding considerations of molecular orbitals the product states are assigned for photolysis at 193 and 248 nm. 31 refs., 14 figs., 2 tabs.

DOE Contract Number:
AC03-76SF00098
OSTI ID:
5525888
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 97:39; ISSN 0022-3654
Country of Publication:
United States
Language:
English