Abstract
The short-time dynamics of a nonstationary state is here determined by a direct inversion of an experimentally measurable Raman excitation profile. The procedure is based on the analytic properties of the Raman scattering amplitude and is best implemented within the maximum entropy formalism. A computational example for resonance Raman excitation profiles in the B state of iodobenzene is presented.
Original language | English |
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Pages (from-to) | 267-270 |
Number of pages | 4 |
Journal | Chemical Physics Letters |
Volume | 205 |
Issue number | 2-3 |
DOIs | |
State | Published - 9 Apr 1993 |