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  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 21 (1990), S. 629-634 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Analytical expressions for the depolarization ratio and reversal coefficient in vibrational polyatomic Raman scattering are derived using the wave packet formulation. Some changes in the dispersion of the depolarization ratio and reversal coefficient caused by changes in the vibronic coupling and by various shifts of nuclear equilibrium positions on molecular electronic excitation which have not been reported before have been studied.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 585-589 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It is shown that the interaction between identical chromophores of freely orienting rigid bichromophoric molecule described by the non-diagonal elements of the molecular damping matrix may lead to unusual dispersion of the depolarization ratios of Raman bands. The forms of the predicted dispersion curves depend on the mechanism for the occurrence of a Raman band and on the mutual orientation of the chromophores. The dispersion curves have anomalous extrema at the frequency of the pure electronic transition of the molecule, i.e. at the maxima of the excitation profiles of Raman lines in an examined frequency field, in contrast to known dispersion curves of the depolarization ratio, the extrema of which are often found to coincide with minima rather than maxima in the excitation profile. This circumstance favours the experimental observation of the predicted curves. Also presented is an excitation profile of the vibrational Raman optical activity signal for such randomly oriented molecules with optically inactive chromophores. This profile has one sign only, unlike the double-signed spectrum of circular dichroism for such molecules. This makes the recording of this profile under conditions of inhomogeneous broadening of spectral lines more convenient than recording the circular dichroism spectrum.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 17 (1986), S. 125-127 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The expressions for the pulse shapes of secondary radiation in the frequency range of Rayleigh scattering and resonance fluorescence and in the range of Raman scattering and shifted resonance fluorescence are obtained on the basis of the quantum treatment of transformation of light pulses, the resonance conditions for Raman and Rayleigh scattering being considerably different. The characteristic cases of different pulse shapes of Raman and Rayleigh scattering are considered for the condition when the molecules are irradiated by light pulses which are shorter then the lifetime of the excited state of the molecule and are weak enough not to result in saturation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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