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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 1702-1717 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Electronic excitations along sites that undergo spatial and temporal fluctuations due to conformational chain motion have been studied in the picture of the stochastic master equation by means of the dynamic Monte Carlo (DMC) and the cumulant expansion (CE) approach. An incoherent site-to-site hopping which is adiabatic relative to the changes of conformational site coordinates has been assumed. The elementary act of conformational change has been considered to be fast, whereas the electronic transfer during the time period of the conformational event has been assumed to be negligibly small. The time evolution of electronic intersite coupling is thus controlled by chromophore sites that, in particular, correspond to the conformational minima of the potential energy landscape. The generalized equations of motion adapted for both the DMC and the CE analysis have been reduced to formulate donor site excitation probabilities 〈Piexc(t)〉 and donor excitation survival functions 〈PD(t)〉 for a simplified chain. In this polymer model, (i) specific nearest-neighbor electronic coupling occurs with two distinct transfer rates W1 and W2 corresponding to two different spatial arrangements of the pendant sites in the pair and (ii) transitions between two definite conformational states occur both in the correlated and in the uncorrelated regime. For short chains and a moderate number of sites in the rotational dyads the whole range from the dynamic to the static limit in the interplay between excitation transfer and correlated conformational motion has been calculated by the DMC method. By means of the cumulant technique well-behaved solutions could be obtained only in the fast conformational transition regime which allows a direct comparison with the DMC results. For longer chains up to 100 sites, in the limit case of uncorrelated conformational motion, preliminary cumulant approaches have been given which, for very rapid conformational rates, agree well with the dynamic effective medium approximation (DEMA) solutions. © 1996 American Institute of Physics.
    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 108 (1998), S. 7023-7034 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Incoherent electronic excitation transport (EET) along chromophore-sites has been studied in the presence of conformational and librational motion by using a rotor chain model as the mobile vehicle. The time-evolution of the electronic site excitation probability vector Pexc(t) averaged by conformational-librational dynamic disorder has been calculated by a second-order cumulant expansion (CE) approach. A master equation for conformer distributions in torsional space has been used [G. J. Moro, J. Chem. Phys. 94, 8577 (1991) and J. Chem. Phys. 97, 5749 (1992)] to describe the coupled, motional stochastic dynamics of a rotor chain. Based upon this model, the correlation functions of excitation transfer rates, important for the calculation of the second cumulants of the stochastic excitation transfer rate matrices, have been constructed. A simplified procedure for evaluating the correlation functions for the L steep minima of torsional angle-dependent symmetrical potentials of nearest-neighbor rotor-pairs and for a Gaussian distribution of torsional angles displacement has been carried out. By using analytical fits to the second cumulants, the evolution of excitation energy transfer has been calculated in terms of the averaged site probabilities 〈Pexc(t)〉 for chromophores, substituted to the L-fold symmetric rotors. The calculated profiles show a pronounced dependence on the curvature ratio in the saddle point of the rotor pair potential, on the number of the pair potential minima as well as on the average of the mean-square deviation of torsional angles from the stable conformations. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics 186 (1994), S. 41-52 
    ISSN: 0301-0104
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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