Abstract
The resonant Raman scattering spectra of vibrationally highly excited SO2 molecules with the vibrational energy of ∼3.7×104 cm-1 exhibit relatively wide (∼50 cm-1) structurized bands. This spectral width is attributed to the mixing of vibrational levels of the ground electronic state 1A1 due to a non-adiabatic interaction with the vibrational levels of the electronically excited state 1B1.
Original language | English |
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Pages (from-to) | 131-137 |
Number of pages | 7 |
Journal | Applied Physics B Photophysics and Laser Chemistry |
Volume | 49 |
Issue number | 2 |
DOIs | |
State | Published - Aug 1989 |
Externally published | Yes |
Keywords
- 33.20.Fb
- 33.50Hv
- 34.30.+h