The determination of time cross correlation functions by inversion of Raman excitation profiles

F. Remacle; R. D. Levine; J. L. Kinsey

doi:10.1016/0009-2614(93)89241-9

The determination of time cross correlation functions by inversion of Raman excitation profiles

F. Remacle^*
, R. D. Levine
, J. L. Kinsey

^*Corresponding author for this work

Institute of Chemistry

Research output: Contribution to journal › Article › peer-review

16 Scopus citations

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
Pages (from-to)	267-270
Number of pages	4
Journal	Chemical Physics Letters
Volume	205
Issue number	2-3
DOIs	https://doi.org/10.1016/0009-2614(93)89241-9
State	Published - 9 Apr 1993

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title = "The determination of time cross correlation functions by inversion of Raman excitation profiles",

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.",

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AU - Kinsey, J. L.

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N2 - 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.

AB - 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.

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The determination of time cross correlation functions by inversion of Raman excitation profiles

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