Possible rotationally resolved detection of NO2 in the C̃ 2A2 state by optical–optical double resonance spectroscopy
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.461425
Reference12 articles.
1. Observation of the Ã(2B2) and C̃(2A2) states of NO2 by negative ion photoelectron spectroscopy of NO−2
2. The electronic structure of nitrogen dioxide. I. Multiconfiguration self‐consistent‐field calculation of the low‐lying electronic states
3. Fluorescence of NO2 in the 2 2B2 state and its application to the optical–optical double resonance (OODR) study of the complex visible spectrum
4. Rovibronic levels of NO2 excited at 514 nm and probed by an optical-optical double-resonance method
5. Optical–optical double resonance of NO2 in the region of 612–614 nm: The role of 2A1 vibronic levels as dark and perturbing state
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1. Ab Initio-Based Global Double Many-Body Expansion Potential Energy Surface for the First 2A″ Electronic State of NO2;The Journal of Physical Chemistry A;2012-03-09
2. Born−Oppenheimer Symmetry Breaking in the C̃ State of NO2: Importance of Static and Dynamic Correlation Effects;The Journal of Physical Chemistry A;2008-03-01
3. Zeeman quantum-beat spectroscopy of NO2: Eigenstate-resolved Landé gF factors near dissociation threshold;The Journal of Chemical Physics;2002-01-08
4. On the energy dependence of the hyperfine interaction in excited states of NO2;The Journal of Chemical Physics;2001-11-15
5. Spin-restricted Brueckner orbitals for coupled-cluster wavefunctions;The Journal of Chemical Physics;1997-12-15
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