Intersystem Crossing and Nonadiabatic Product Channels in the Photodissociation of N2O4 at 193 nm
Author:
Affiliation:
1. Department of Chemistry and the James Franck Institute, The University of Chicago, Chicago, Illinois 60637
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp993651u
Reference36 articles.
1. Absorption cross-sections of NO2 in the UV and visible region (200 – 700 nm) at 298 K
2. Extinction coefficients of NO2 and N2O4
3. The dimeric nitrogen oxides. Part I. Electronic absorption of the nitrogen oxide dimer, and comparison of observed and calculated spectra for dinitrogen dioxide, trioxide, and tetraoxide
4. Ab initio multiple reference double‐excitation configuration‐interaction ground and excited state potential curves for nitromethane decomposition
5. The lower electronic states of nitrite and nitrate ion, nitromethane, nitramide, nitric acid, and nitrate esters
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1. Production and Photodissociation of the Methyl Perthiyl Radical;The Journal of Physical Chemistry A;2016-02-25
2. The electronic spectrum and photodissociation of dinitrogen tetroxide (N2O4): Multireference configuration interaction studies;The Journal of Chemical Physics;2010-10-14
3. The Diabatic Picture of Electron Transfer, Reaction Barriers, and Molecular Dynamics;Annual Review of Physical Chemistry;2010-03-01
4. Photodissociation of NO2 in the (2)B22 state: A slice imaging study and reinterpretation of previous results;The Journal of Chemical Physics;2008-10-21
5. Multiconfigurational self-consistent field and multireference internally contracted configuration interaction studies on the excited states of weakly bonded NO2 dimer (N2O4);The Journal of Chemical Physics;2007-11-28
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