THE DETERMINATION OF TIME CROSS-CORRELATION FUNCTIONS BY INVERSION OF RAMAN EXCITATION PROFILES

被引：21

作者：

REMACLE, F

LEVINE, RD

KINSEY, JL

机构：

[1] RICE UNIV,RICE QUANTUM INST,HOUSTON,TX 77251

[2] RICE UNIV,DEPT CHEM,HOUSTON,TX 77251

[3] UNIV LIEGE,DEPT CHIM,FNRS,B-4000 LIEGE 1,BELGIUM

来源：

CHEMICAL PHYSICS LETTERS | 1993年 / 205卷 / 2-3期

基金：

美国国家科学基金会;

关键词：

D O I：

10.1016/0009-2614(93)89241-9

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

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.

引用

页码：267 / 270

页数：4

共 37 条

[1] ALGORITHM FOR FINDING THE DISTRIBUTION OF MAXIMAL ENTROPY [J].