Literature DB >> 12626736

Two-dimensional femtosecond spectroscopy.

David M Jonas1.   

Abstract

The simplest two-dimensional (2D) spectra show how excitation with one (variable) frequency affects the spectrum at all other frequencies, thus revealing the molecular connections between transitions. Femtosecond 2D Fourier transform (2D FT) spectra are more flexible and share some of the remarkable properties of their conceptual parent, 2D FT nuclear magnetic resonance. When 2D FT spectra are experimentally separated into real absorptive and imaginary refractive parts, the time resolution and frequency resolution can both reach the uncertainty limit set for each resonance by the sample itself. Coherent four-level contributions to the signal provide new molecular phase information, such as relative signs of transition dipoles. The nonlinear response can be picked apart by selecting a single coherence pathway (e.g., specifying the relative signs of energy level difference frequencies during different time intervals as in the photon echo). Because molecules are frozen on the femtosecond timescale, femtosecond 2D FT experiments can separate a distribution of instantaneous molecular environments and intramolecular geometries as inhomogeneous broadening. This review provides an introduction to two-dimensional Fourier transform experiments exploiting second- and third-order vibrational and electronic nonlinearities.

Year:  2002        PMID: 12626736     DOI: 10.1146/annurev.physchem.54.011002.103907

Source DB:  PubMed          Journal:  Annu Rev Phys Chem        ISSN: 0066-426X            Impact factor:   12.703


  93 in total

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Authors:  Yung Sam Kim; Robin M Hochstrasser
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Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-04       Impact factor: 11.205

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Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-13       Impact factor: 11.205

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