Collision-induced rotational transitions in electronically excited states: the application of dipole-type selection rules to SO2 (Ã1A2)
- 15 October 1980
- journal article
- Published by Elsevier in Chemical Physics Letters
- Vol. 75 (2) , 249-253
- https://doi.org/10.1016/0009-2614(80)80506-9
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Single rovibronic level lifetimes of the 1A2 state of SO2 excited in the 3043 Å (“E”) band: rotationally resolved fluorescence emission spectrumChemical Physics Letters, 1980
- Kinetics of fluorescence decay of SO2 excited in the 2662–3273 Å regionInternational Journal of Chemical Kinetics, 1978
- Theory of collision induced intersystem crossing. Application to glyoxalChemical Physics Letters, 1976
- Rotational Structure in the Absorption Spectrum of SO2 between 3000 Å and 3300 ÅCanadian Journal of Physics, 1975
- Relaxation in the 1A u state of glyoxal. II. Collisional quenchingThe Journal of Chemical Physics, 1975
- Time-resolved fluorescence kinetics and 1B1(1Δg) vibronic structure in tunable ultraviolet laser excited SO2 vaporThe Journal of Chemical Physics, 1974
- Collision induced intersystem crossing the photophysics of glyoxal vapor excited at 4358 ÅChemical Physics, 1973
- Some Propensity Rules in Collision-Induced Rotational Quantum JumpsThe Journal of Chemical Physics, 1970
- Energy-Transfer Processes in Monochromatically Excited Iodine Molecules. I. Experimental ResultsThe Journal of Chemical Physics, 1965
- Rotational, Vibrational, and Electronic Energy Transfer in the Fluorescence of Nitric OxideThe Journal of Chemical Physics, 1963