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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 57 (1979), S. 641-646 
    ISSN: 1432-1440
    Keywords: Mitochondria ; Membranes ; Cytochrome oxidase ; Fluorescence methods ; Electron microscopy ; Mitochondrien ; Membranen ; Cytochromoxidase ; Fluoreszenzmethoden ; Elektronenmikroskopie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Biologische Membranen sind im wesentlichen asymmetrische zwei-dimensionale Lösungen von Proteinen in einer bimolekularen Lipidschicht. Das allgemeine Aufbauprinzip und viele physikalische Eigenschaften biologischer Membranen lassen sich dadurch erklären, daß sowohl die Membranproteine als auch die Membranlipide hydrophile und hydrophobe Stellen besitzen. Die meisten biologischen Eigenschaften einer Membran werden durch die Membranproteine bestimmt, die richtungsgebundene Prozesse katalysieren können. Anhand des Membranproteins Cytochromoxidase wird gezeigt, wie die räumliche Anordnung von Membranproteinen durch chemische, fluorometrische und elektronenoptische Methoden studiert werden kann. In den meisten Fällen ist es allerdings heute noch nicht möglich, die Funktionen einer Membran aufgrund ihres molekularen Bauprinzips zu erklären.
    Notes: Summary Biological membranes are essentially asymmetric two-dimensional solutions of proteins in a bimolecular lipid layer. The overall structure and many physical properties of biological membranes can be explained by the fact that membrane proteins and membrane lipids contain hydrophilic as well as hydrophobic domains. Most biological properties of the membrane are determined by the membrane proteins which can catalyze directional processes. With the membrane protein cytochrome oxidase it will be demonstrated how the three-dimensional arrangement of membrane proteins can be studied by chemical, fluorometric, and electron optical methods. However, it is in most cases still impossible to explain the function of a membrane on the basis of its molecular architecture.
    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 88 (1988), S. 7942-7951 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: This paper presents a combined experimental and theoretical study of the hyper-Raman spectrum of pyridine adsorbed onto roughened silver electrodes. The surface enhanced hyper-Raman spectra (SEHRS) were measured using a focused cw mode-locked Nd:YAG laser with a peak power density of approximately 107 W/cm2 . Dominant bands in the pyridine spectra are the same (totally symmetric) bands as have been seen in the corresponding Raman (SERS) spectrum, although the relative intensities are different. To interpret these spectra, we present a semiempirical molecular orbital method for determining excitation energies, polarizability derivatives, and hyperpolarizability derivatives that is based on the π-electron Pariser–Parr–Pople (PPP) method. An empirical molecular force field is used to derive vibrational information, and the accuracy of the spectra is assessed by comparison with normal Raman spectra for liquid pyridine and with SERS spectra. The resulting SEHRS spectra are in good agreement with the measured spectra, particularly with respect to the intensity changes in the dominant lines in going from SERS to SEHRS. In addition, the theoretical/experimental comparisons indicate that SEHRS is more sensitive to adsorbate orientation than is SERS since the nontotally symmetric modes are predicted to be comparable in SEHRS (but not SERS) intensity to the totally symmetric modes for orientations other than perpendicular. Most important, a comparison of theoretical and experimental SEHRS/SERS ratios suggests that the enhancement factor associated with SEHRS is on the order of 1013 which is much larger than the 106 enhancement seen for SERS.
    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 87 (1987), S. 4189-4200 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present a combined experimental/theoretical study of the coverage and frequency dependence of surface (enhanced) resonance Raman scattering [S(E)RRS] of cobalt phthalocyanine (CoPc) on CaF2 roughened silver films. The experimental spectra indicate a rather strong coverage dependence at very low coverage for excitation at or close to the molecular resonance frequency, with a peak at 0.07 monolayer (ML) followed by a rapid decrease above that. This coverage dependence differs strongly with observations on smooth films, where a much weaker dependence is observed. At very low coverage on the rough Ag films S(E)RRS enhancements comparable to SERS are observed. To model this coverage dependence, we consider the electromagnetic interactions between the adsorbate and substrate, with the substrate modeled as a metal spheroid and the adsorbate as a layer with variable coverage. Two models for this layer are considered, an effective medium model in which the layer is taken to have a coverage dependent dielectric constant, and a coupled dipole model in which both the molecules and metal are taken to be polarizable dipoles. The dependence of field enhancement and S(E)RRS intensity is studied for these two models as a function of frequency, coverage, and Stokes shift. It is found that although there are differences between the two models, the coverage dependence is similar in both, with peak intensities at about 0.1 ML for reasonably prolate spheroids. These models also demonstrate that the drop in intensity above 0.1 ML arises from damping of the plasmon resonance by the adsorbed layer. Interadsorbate interactions are found to play a role in determining the coverage dependence of the S(E)RRS intensity that is secondary to this damping. The large enhancements seen below 0.1 ML suggest that excited state quenching by the surface is not important for this nonfluorescent molecule.
    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 88 (1988), S. 5481-5488 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Collisional energy transfer from H atoms to CO(v=0, J(approximately-equal-to)2) has been studied at a collision energy of 1.58±0.07 eV by photolyzing H2S at 222 nm in a nozzle expansion with CO and probing the CO(v‘, J‘) levels using tunable VUV laser-induced fluorescence. The ratio CO(v‘=1)/CO(v‘=0) is found to be 0.1±0.008. The rotational distribution of CO(v‘=0) peaks at J‘≤11 and decays gradually; population is still observed at J‘≥45. The rotational distribution of CO(v‘=1) is broad and peaks near J‘=20. The experimental results are compared to quasiclassical trajectory calculations performed both on the H+CO surface of Bowman, Bittman, and Harding (BBH) and on the surface of Murrell and Rodriguez (MR). The experimental rotational distributions, particularly those for CO(v‘=1), show that the BBH surface is a better model than the MR surface. The most significant difference between the two surfaces appears to be that for energetically accessible regions of configuration space the derivative of the potential with respect to the CO distance is appreciable only in the HCO valley for the BBH surface, but is large for all H atom approaches in the MR potential. Because the H–CO geometry is bent in this valley, vibrational excitation on the BBH surface is accompanied by appreciable rotational excitation, as observed experimentally.
    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 88 (1988), S. 3709-3714 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The self-consistent field (SCF) approximation for coupled anharmonic vibrations is applied to the calculation of vibrational energy levels (predissociation resonances) of collinear models of I2 (v)He and I2 (v)Ne, with vibrational quantum number v between 5 and 30. The predissociation lifetimes of these same states are obtained from a distorted wave Born approximation calculation with self-consistent field states taken as the initial states of the complex, and with correlation between the modes taken as the interactions leading to decay. Although the binding energies of the van der Waals complex are very small (order of several cm−1 ), the SCF eigenvalues are in remarkable agreement with the exact numerical values. The lifetimes obtained from the SCF-distorted wave Born approximation (DWBA) are compared with calculations in which the initial state is treated more simply, assuming separability of the modes involved. Results then show that the DWBA with SCF initial states is considerably more accurate than with the more primitive initial state choice. We conclude from these results that the self-consistent field method offers a very accurate description of large-amplitude vibrational motions in van der Waals clusters, with good quantitative results for both the energy levels and predissociation dynamics of these species.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 7712-7712 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 2987-2993 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Methods are developed for modeling the optical properties of aggregates of large numbers of small metal nanospheres in a dielectric medium. Aggregates are modeled as systems of coupled dipoles, with the dipole polarizabilities for the spheres determined using Mie theory. Fast-Fourier-transform (FFT) and conjugate-gradient (CG) techniques are used to solve the electrodynamic equations for both ordered and disordered aggregates. Results are shown to match solutions arrived at by direct methods. The range of validity of the coupled-dipole approximation for modeling DNA-linked colloidal materials is established by comparison with coupled-multipole results. While the methods are applicable only to lattice gas aggregates and aggregates composed of nanospheres on cubic lattices, there are no restrictions as to aggregate shape. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 22 (1966), S. 579-584 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 22 (1966), S. 585-590 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 37 (1969), S. 996-1001 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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