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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 5711-5721 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The complex semiclassical formalism of Robert and Bonamy is used to calculate both half widths and line shifts for water vapor in a bath of nitrogen. The assumed intermolecular potential is a combination of electrostatic, Lennard-Jones 6-12 atom–atom, induction, and dispersion terms. The complex valued resonance functions have been previously evaluated when the assumed potential was electrostatic only. In this work these functions are evaluated when the potential is extended to include the atom–atom terms. Calculations made in the 3ν1+ν3 vibrational band of H2O are in good agreement with experimental results for both the half width and line shifts. It is shown that the imaginary parts are important for both the line shift and half width calculations. © 1996 American Institute of Physics.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 1325-1330 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: We study the effect of surface roughness on magnetic domain wall thickness, domain size, and coercivity of thin magnetic films. We show that the roughness increases (decreases) the domain wall thickness and domain size for Bloch walls (Néel walls). The surface roughness affects the domain wall movement and causes the increase of coercivity for Néel walls. The coercivity due to domain rotation for Bloch walls decreases with the increase of roughness. The domain wall thickness, domain size, and coercivity are each related to the demagnetizing factor, which depends on the roughness and type of wall (Bloch wall or Néel wall). The calculated coercivity versus thickness is compared with experimental data of ultrathin Co films, where the thickness dependent roughness parameters are available. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 6495-6505 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: State-to-state relaxation rates have been determined for ozone in collisions with itself and with nitrogen by two different methods. A theoretical model of collisional broadening of ozone lines, the quantum Fourier transform theory with improved dynamics, was adapted to compute state-to-state inelastic contributions to the pressure-broadened halfwidths for ozone–nitrogen collisions. These quantities were then determined experimentally using time-resolved infrared double resonance spectroscopy and a kinetic model for relaxation. Comparisons of kinetic model simulations and experimental double-resonance signals confirmed a propensity for first-order dipolar transitions, but also clearly demonstrated the importance of higher-order interactions leading to large changes in J in single collisions. Simple energy and angular-momentum-scaling laws were found to be inadequate to represent the experimental data.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 9412-9421 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Widths and shifts of methane lines perturbed by nitrogen are calculated using a complex-valued implementation of Robert–Bonamy (RB) theory. The static intermolecular potential is described as a sum of electrostatic forces and Lennard-Jones (6-12) atom–atom terms, using literature values for all physical parameters. Vibrational dependence of the isotropic potential is obtained from the polarizability of methane assuming a dispersion interaction. The repulsive part of the Lennard-Jones accounts for the greatest part of widths, while dispersion interactions are largely responsible for shifts. Although the average error between calculated and observed linewidths (up to J=8) is less than 6%, their distribution suggests the influence of interactions not described in the present theory. © 1994 American Institute of Physics.
    Materialart: Digitale Medien
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  • 5
    facet.materialart.
    Unbekannt
    Saranac Lake, N.Y., etc. : Periodicals Archive Online (PAO)
    Management Review. 70:10 (1981:Oct.) 21 
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  • 6
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 1821-1845 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Laser Raman spectra of the trinucleoside diphoshate ApApA and dinucleoside phosphates ApU, UpA, GpC, CpG, and GpU are reported and discussed. Assignments of conformationally sensitive frequencies are-facilitated by comparison with spectra reported here of poly(rA), poly(rC), and poly(rU) in deuterium oxide solutions. The significant spectral differences between ApU and UpA, and between GpC and CpG, reveal that the sequence isomers have nonidentical conformations in aqueous solution. In UpA at low temperature the bases are stacked and the backbone conformation is similar to that found in ordered polynucleotide structures and RNA. In ApU no base stacking can be detected and the backbone conformation differs from that found in UpA, both in the orientation of phosphodiester linkages and in the internal conformation of ribose. At the conditions employed neither ApU nor UpA exhibits base pairing in aqueous solutions. In both GpC and CpG the bases are stacked and the phosphodiester conformations are similar to those encountered for UpA and RNA. However, major differences between spectra of GpC and CpG indicate that the geometries of stacking and ribosyl conformations are different. In GpC the Raman data favor the formation of hydrogen bonded dimers containing GC pairs. Protonation of C in GpC is sufficient to eliminate the ordered conformation detected by Raman spectroscopy. Despite the ordered backbone conformation evident in GpU, this dinucleoside apparently contains neither stacked nor hydrogen bonded bases at the conditions employed here. The Raman data also confirm the stacking interactions in ApApA, poly(rA), and poly(rC) but suggest that the backbone conformation in poly(rC) differs qualitatively from that found in most ordered polynucleotide structures and is thermally more stable. The present results demonstrate the sensitivity of the Raman technique to sequence-related structural differences in oligonucleotides and provide additional spectra-structure correlations for future conformational studies of RNA by laser Raman spectroscopy.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
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