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  • Electronic Resource  (4)
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  • Electronic Resource  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 94 (1990), S. 7834-7839 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 51-54 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The depolarization of the totally symmetric (ν1) Raman band of liquid carbon tetrachloride has been measured at 22 °C and pressures up to the freezing pressure of 1.1 kbar using the scattering geometry Z(YZ)Y, which causes little depolarization by the windows. The depolarization decreases linearly from 6.5×10−3 at zero pressure to 5.6×10−3 at 1.15 kbar. The change is explained as the resultant of a decrease of both the vibrational amplitude and the mean intermolecular distance under pressure.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 1836-1840 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of pressure on the reorientational and the vibrational phase correlation times of liquid carbon disulfide has been determined up to 10 kbar at 295 K from the widths of the isotropic and anisotropic components of the Raman ν1 band. The reorientational correlation time increases with pressure from 1.3 ps at 1 bar to 9 ps at 10 kbar, and the vibrational dephasing time decreases from 19 ps at 1 bar to 5 ps at 10 kbar. The reorientational correlation time is linear in the shear viscosity, and the slope agrees well with the hydrodynamic estimate based on slip at the boundary and the assumption that the carbon disulfide molecule is prolate. The correlation times reported in Ref. 20 at 164–310 K at ambient pressure are the same function of the viscosity divided by the temperature as our values, so showing that the correlation time varies in the same way with the viscosity divided by the temperature whether the viscosity is varied by varying the temperature at constant pressure or by varying the pressure at constant temperature. The correlation time extrapolated to zero viscosity agrees well with the correlation time of a classical free rotor. Schweizer and Chandler's kinetic model for vibrational dephasing reproduces the dephasing time within the experimental precision over the experimental pressure range, whereas the hydrodynamic model agrees well with experiment at atmospheric pressure but predicts a dephasing time at 10 kbar that is 2/5 of the experimental value.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 2538-2547 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of pressure on the polarized and depolarized Raman spectra of liquid carbon disulphide, i.e., the peak frequencies, bandwidths, and relative intensities of both the allowed ν1 and 2ν2 bands and the interaction-induced ν2 and ν3 bands, have been measured at 22 °C up to 10 kbar. This paper discusses the effect of pressure on the frequencies and on the relative isotropic intensity of the ν1 and 2ν2 bands. The frequency of the ν1 band increases linearly with pressure, within the experimental uncertainty, at the rate 0.16±0.01 cm−1 kbar−1, and the frequencies of the ν2, ν3, and 2ν2 bands decrease nonlinearly. The frequency shifts are described by second-order perturbation theory with the molecular anharmonicity and the intermolecular interaction as perturbations. The leading terms of the shifts consist of the same derivative of the interaction potential, multiplied by different anharmonicity constants, and the shifts of the ν1 and 2ν2 bands suggests that the C–S bond length decreases at the rate 2×10−4 A(ring) kbar−1. The relative isotropic intensity of the 2ν2 and ν1 bands increases with pressure at the rate 0.050 kbar−1, whereas the anisotropic 2ν2 intensity relative to the isotropic ν1 intensity is independent of pressure to the experimental precision of ∼0.005. The effect of pressure on the second derivative of the isotropic and anisotropic parts of the polarizability with respect to the bend coordinate was estimated as 1.1×10−43 C m2 V−1 kbar−1 and ∼0, respectively, from these values.
    Type of Medium: Electronic Resource
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