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  • 1
    Signatur: PIK M 370-95-0206
    Materialart: Monographie ausleihbar
    Seiten: 325 S.
    Ausgabe: 2. unveränderter Nachdruck
    ISBN: 3893191313
    Standort: A 18 - Bitte bestellen
    Zweigbibliothek: PIK Bibliothek
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 2194-2207 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 3112-3123 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Temperature quench echoes are analyzed in terms of the temperature–temperature correlation function in the harmonic approximation, and the resulting expressions are compared with molecular dynamics simulations. The relationship between the time dependence of the echo depth and the density of states is demonstrated for harmonic systems. For a protein, which has significant anharmonicity, the time dependence is dominated by relaxation effects that originate from dephasing of the periodic motions. A simple relaxation model is shown to provide a good description of the results observed in the simulations. © 1995 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 3124-3139 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A new echo phenomenon in proteins, a generalization of so-called temperature quench echoes, is introduced and shown to reveal, through molecular dynamics simulations, periodic motions (normal modes) in proteins with phase coherence times of about one picosecond. The echoes are induced through reassignments of Cartesian velocities to protein atoms at times t=0 and t=τ (0〈τ≤1 ps) and appear as two sharp (widths of about 5 fs) features in the kinetic and potential energy at t=3τ/2 and t=2τ. The velocities, assigned at t=0 and at t=τ to each atom, need to be correlated, but can otherwise be random. The echo at 3τ/2 can be induced without any change in the temperature of the protein. Skeletal motions involving angular and stretch motions contribute principally to the echo effect. Electrostatic interactions do not affect the echoes. The echoes in the temperature are described, in the framework of the harmonic approximation, in terms of the equilibrium temperature–temperature correlation function. The velocity reassignments induce the echoes through the generation of phase coherence of protein modes. Phase relaxation due to anharmonic interactions, lead to a dependence of the echo depths on the time interval τ between velocity replacements which can be accounted for by phase diffusion or by Langevin oscillators. The echo effect can provide a sensitive probe for the study of non-diffusive energy transport in proteins. © 1995 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 84 (1986), S. 5155-5161 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: We show that magnetic field effects observed on reactions between two paramagnetic end groups of a polymer can be explained through the folding motion of the polymer. This folding stochastically alters the exchange interaction between the paramagnetic end groups and, thereby, affects their spin dynamics. We describe the resulting stochastic quantum system by a (Monte Carlo) computer simulation as well as by a new approximation which involves the spectrum of the stochastic interaction. This approximation can be of general use for the description of stochastic quantum systems when a diagonal stochastic interaction originates from an arbitrary, i.e., nonlinear and non-Gaussian, stochastic process.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 151-160 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The generalized moment expansion has previously only been used to provide an effective algorithm for the approximation of the time dependence of observables connected with reactive Brownian processes. We extend this algorithm to describe the relaxation of observables in nonreactive processes. The wide applicability of the method is demonstrated for various examples: equilibrium correlation functions like autocorrelation functions and dynamic structure factors, particle number correlation functions monitoring diffusive redistribution, and barrier crossing problems.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 85 (1986), S. 6602-6609 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: A correct description of the electronic excitations in polyenes demands that electron correlation is accounted for correctly. Very large expansions are necessary including many-electron configurations with at least one, two, three, and four electrons promoted from the Hartree–Fock ground state. The enormous size of such expansions had prohibited accurate computations of the spectra for polyenes with more than ten π electrons. We present a multireference double excitation configuration interaction method (MRD-CI) which allows such computations for polyenes with up to 16 π electrons. We employ a Pariser–Parr–Pople (PPP) model Hamiltonian. For short polyenes with up to ten π electrons our calculations reproduce the excitation energies resulting from full-CI calculations. We extend our calculations to study the low-lying electronic excitations of the longer polyenes, in particular, the gap between the first optically forbidden and the first optically allowed excited singlet state. The size of this gap is shown to depend strongly on the degree of bond alternation and on the dielectric shielding of the Coulomb repulsion between the π electrons.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 84 (1986), S. 4015-4025 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The generalized moment expansion provides an effective algorithm for the approximation of the time dependence of observables that monitor stochastic processes. Up to now this method had been applied mainly to one-variable birth–death processes or to one-dimensional Fokker–Planck systems since in these cases analytical and numerical methods for the evaluation of the generalized moments were available. Here we demonstrate that numerical sparse matrix methods can be used to extend the range of application of the generalized moment expansion to higher dimensions. For this purpose we introduce a simple but general discretization scheme for Fokker–Planck operators of Smoluchowski type which is, for these special operators, superior to common numerical discretization schemes for differential operators. As an application we determine the Mössbauer absorption spectrum of a Brownian particle in certain two- and three-dimensional potentials. This serves as a model for the motion of the heme group in myoglobin.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 82 (1985), S. 2147-2160 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: On the basis of solutions to two-dimensional diffusion-reaction equations the fluorescence signal for photobleaching experiments with arbitrary time-dependent and time-independent irradiation profiles is evaluated. The solutions involve spatial discretization and spectral expansion, spatial and temporal discretization employing the Crank–Nicholson integration scheme, generalized moment expansion, and an approximation yielding an analytical expression. The algorithms developed can be installed on small computers to determine lateral diffusion coefficients from observed fluorescence signals. The theory developed is applied to photobleaching with constant irradiation profiles and the resulting diffusion coefficients, in the range 0.001 to 10.0 μm2 s−1 for the systems investigated, are compared to the results of conventional photobleaching experiments. Applications of the theory compare further the signals resulting from Gaussian and rectangular irradiation profiles, the influence of the membrane geometry, i.e., planar or spherical, on the fluorescence signal, and the effect of finite diffusion spaces.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 3760-3760 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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