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  • Analytical Chemistry and Spectroscopy  (3)
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  • Analytical Chemistry and Spectroscopy  (3)
  • Chemistry  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 16 (1985), S. 137-138 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low-frequency Raman spectra of gaseous formic and acetic acids are corrected from counts per second to the square of the polarizability derivative with respect to the normal coordinate. The acetic acid peak at 98.9 cm-1 is shifted to 106 cm-1 by this correction, necessitating minor reassignments. The intense, broad, 'Rayleigh Line' is greatly reduced by this correction, to reveal scattering by pure rotational motion.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spinning divided Raman liquid cell has been used to measure the relative integrated Raman intensities of several bands of C6H6(I), CCI4(I), C6H12(I), C6D6(I), CH3CN(I), CH2CI2(I), SO42-(aq.), and CIO4 -(aq.) at room temperature. To convert these relative intensities to absolute scattering activities, the average of the eight literature values of the absolute Raman scattering cross-section of the 992 cm-1 band of C6H6(I) under blue or green excitation was used. This yielded an unpolarized scattering activity per molecule of 640 ×10-9 cm4 g-1, with a standard deviation of 80 ×10-9 cm4 g-1 [in SI units, 792 ×10-34 and standard deviation 100 ×10-34 (C m2/V)2/(m2 kg)]. It is suggested that this value can be used as the basis for an interim scale of Raman scattering intensities. The scattering activities on this scale are higher than those in the literature because the benzene calibration value is higher than has been used previously. The relative scattering activities obtained agree well with those of Nestor and Lippincott. It is suggested that fairly weak and depolarized bands are often better secondary standards for relative intensity measurements than the very strong, very polarized bands that have traditionally been used.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 20 (1989), S. 695-699 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The origin of reduction procedures used to transform (or normalize) relative Raman intensities is reviewed and discussed in detail in order to clarify the difference between an approach based on the frequency domain representation of Placzek and that based on the time domain representation of Heisenberg as developed by Gordon. These procedures are not designed to replace standard methods for the measurement of accurate absolute Raman scattered intensity. However, they do provide a practical method for a first-order comparison of Raman spectra for samples measured under different conditions of phase, concentration and temperature and for samples measured with different excitation frequencies. Especially for the low-wavenumber region, reduced spectra allow analyses of significant spectral features: a linear baseline may be more easily defined, which in turn permits easier measurement of peak maxima, band shapes and relative intensities. Further, certain forms of the reduced Raman spectrum may be compared directly with the corresponding infrared absorption spectrum.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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