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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 3984-3986 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    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 113 (2000), S. 8594-8607 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The high resolution magnetic rotation spectrum of a diatomic molecule is considered. A procedure is described for calculation of the magnetic rotation signal in both first and second harmonic for an oscillating magnetic field in the low-field limit. The procedure is simpler than other methods available in the literature, and a more complete account is taken of the various possible contributions to the signal. Perturbations between electronic states that make it possible to observe magnetic rotation signals for high-J transitions are discussed, along with the associated evolution of line shape that complicates frequency measurements from magnetic rotation spectra. Examples are given from a recent magnetic rotation study of the A 3Π1u–X 1Σg+ system of 79Br2. © 2000 American Institute of Physics.
    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 101 (1994), S. 5464-5472 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The laser-induced fluorescence spectrum in ICl of the (2'–0‘) vibrational band in the B 3Π0+–X 1Σ+ electronic system has been measured as a function of the electric field strength up to 32.5 kV/cm. Field-induced intensity measurements on I35Cl have been used to determine the magnitude and sign of the electric dipole moment μB in the B state relative to the magnitude and sign of the moment μX in the X state. From the intensity ratio of the field-induced line Q(0) to the allowed Stark component P(1,0), which has the same upper state, it was found that μB/μX=+(0.888±0.051). The positive sign indicates that the polarity is the same in the B and the X states. Intensity ratio measurements for Q(0) to R(5) and for Q(1) to R(5) yield similar (but less precise) results. In order to test this first application of the method to excited electronic states, Stark shift measurements were carried out on a number of P-branch Stark components. It was found for I35Cl that ||μB/μX||=(0.8984±0.0036), in good agreement with the intensity measurements. The corresponding determination for I37Cl is that ||μB/μX||=(0.900±0.014). The present results are in agreement with those obtained earlier from studies of the absorption spectrum by Watanabe et al. [Jpn. J. Appl. Phys. 31, 901 (1992)].
    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 110 (1999), S. 5568-5577 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have measured the static dipole polarizability of Nay−xLix clusters (with y=2, 3, 4, and 8) by molecular beam deflection technique. For a given size, the polarizability of pure lithium clusters is smaller than the polarizability of pure sodium clusters. For mixed clusters, a smooth decrease in the polarizability is observed as the proportion of lithium atoms increases. For the NaLi molecule, both experimental permanent dipole and average polarizability have been obtained. Experimental results are compared to results of density functional theory and configuration interaction single and double (CISD) ab initio calculations. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 8725-8735 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A high resolution spectroscopic study of HI+ has been carried out for the first time. The absorption spectrum in the inverted 2Π ground electronic state has been measured with a linewidth of 0.004 cm−1 between 1995 and 2245 cm−1. A total of 117 vibration–rotation transitions were observed with a tunable diode laser spectrometer coupled to an ac glow discharge cell employing velocity modulation. Lines were measured in the vibrational fundamental of the 2Π1/2 spin substate and in the three lowest (v+1←v) bands of the 2Π3/2 spin substate. A good fit to the data was obtained using a standard vibration–rotation, fine structure Hamiltonian. Equilibrium values were determined for 16 molecular parameters including the harmonic vibrational frequency ωe, the rotational constant Be, and the Λ-doubling constants pe and qe. A review of the ground state properties of the hydrogen halide ions HX+ (X=F, Cl, Br, I) shows that the harmonic force constant is, to excellent approximation, a linear function of the internuclear spacing. In ten different vibration–rotation transitions of the two spin substates of HI+, hyperfine splittings were observed. A total of 58 relative splittings of hyperfine components were analyzed to determine the iodine quadrupole coupling constant eQq0 as well as the Frosch–Foley magnetic hyperfine constants a, (b+c), and d. The results have been used to investigate the electronic properties of the ion. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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