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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 79 (1975), S. 542-543 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: By use of a free-jet expansion which incorporates a heated nozzle, we have recorded the laser excitation spectrum of the 460 nm band system of NiCl2 at rotational resolution. The rotational temperature in these recordings was about 12 K. Several bands have been recorded and analyzed for three isotopomers, 58Ni35Cl2, 60Ni35Cl2, and 58Ni35Cl37Cl in natural abundance. Spin components with Ω values of 0 and 1 have been identified in both the upper and lower states of the transition. Accurate values for all three vibrational intervals ν1, ν2, and ν3 have been determined for nickel dichloride in the upper state and for the bending wave number ν2 in the lower state. The results show that the molecule is linear in both states involved in the transition and that the lower (ground) state is 3Σ−g in character. Evidence is presented from the nickel isotope shifts to show that the transition is vibronically induced through the bending vibration and that the upper state is vibronically 3Πu in character; it probably derives from an electronic 3Δg state. The zero-point averaged bond lengths are determined for both states as r0′=0.209 435(13) nm and r0″=0.205 317(14) nm. The fine structure parameters for the X˜ 3Σ−g state are interpreted in terms of low lying 1Σ+g and 3Πg states, which are shown to lie a few thousand reciprocal centimeters above the ground state. © 1996 American Institute of Physics.
    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 115 (1993), S. 2978-2979 
    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
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 84 (1986), S. 2481-2488 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rotationally cold spectrum of the B˜ 2Π–X˜ 2Π system of ClCN+ has been obtained by the crossed free jet-electron beam method. The narrowing of vibrational bands has allowed the assignment of many of the major features in the spectrum. The (Cl–C) stretching vibrational frequencies have been determined to be 823 and 526 cm−1 for the ground and excited electronic states, respectively, and the (C 3/4 N) stretching vibrational frequency for the ground electronic state has been determined to be 1915 cm−1. The difference in spin-orbit coupling constants for these two electronic states was also measured in the spectrum to be 87 cm−1. The difference in vibrational frequencies and the difference in spin-orbit coupling constants for these electronic states, in comparison with similar values for the isoelectronic molecules ClC2H+ and SCN, allow a fairly complete picture of the π bonding in these molecules to be formed.
    Type of Medium: Electronic Resource
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