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- W2438535654 abstract "In electronic resonance conditions, rotational Raman cross sections are no longer given by the familiar classical (Placzek-Teller) intensities or vibrational symmetry based polarization selection rules.1-5 Instead the resonance rotational Raman intensities are sensitive functions of the resonant excited state dephasing processes. We describe spontaneous resonance rotational (rovibrational) Raman scattering in a rovibronic Kramers-Heisenberg tensorial framework. Inclusion of the explicit angular dependence of molecular states allows the intensities and polarization characteristics of the resonant secondary radiation of isolated molecules to be properly captured." @default.
- W2438535654 created "2016-06-24" @default.
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- W2438535654 date "1990-05-21" @default.
- W2438535654 modified "2023-09-22" @default.
- W2438535654 title "Resonance Raman studies of subrotational period photodissociation of isolated molecules" @default.
- W2438535654 hasPublicationYear "1990" @default.
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