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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 84 (1986), S. 6218-6226 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rate constants and associated kinetic parameters for the methyl nitrite conformational interconversion process have been determined at low pressures (∼5–70 Torr) where the kinetics are very nearly second order. Comparisons with model calculations demonstrate that vibrational redistribution is statistical and very nearly ergodic in methyl nitrite molecules possessing ∼12 kcal mol−1 internal energy.
    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 82 (1985), S. 3996-4006 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Bimolecular region unimolecular rate constants for the syn=anti conformed exchange in gaseous methyl nitrite and in methyl nitrite–bath gas (bath gases being He, Ne, Ar, H2, N2, O2, CO, CO2, NH3, SF6, CH4, C2H6, C3H8, n-C4H10, and n-C5H12) were obtained from line shape analysis of 200 MHz 1H NMR spectra. The pressure dependent rate constants were analyzed to yield relative bimolecular collisional activation efficiencies βMp on a pressure per pressure basis for each bath gas. The resulting βMp indicate that, for methyl nitrite conformational interconversion, which occurs at a low threshold energy, E0=11.70 (0.40) kcal/mol, and a low vibrational state density ρ(E0)=160 states/cm−1 intermolecular collisional energy transfer is dominated by the attractive portion of the intermolecular potential, with the energy transfer in the collisional complex being statistical. Corrections to previously published data are given.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 106 (1984), S. 7638-7639 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 273-276 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polarized and depolarized Raman spectra of the ν6 (C—C3 stretch), ν7 (C—Cl stretch) and ν8 (C—C3 bend) modes of tert-butyl chloride have been studied as a function of temperature in the liquid phase. Isotropic correlation times for the bending mode were found to be 3-4 times longer than values obtained for the two stretching vibrations. An analysis of the isotropic correlation functions using the Kubo lineshape formalism revealed that the less efficient vibrational relaxation of the deformation arises primarily from the lower second monents of this mode. Reorientational times calculated from the two stretching vibrations were almost three times shorter than the earlier reported dipolar relaxation time, indicating that the tumbling motion of tert- butyl chloride is close to the small-step diffusion limit.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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