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Charge transport range

The above statements are valid for monomolecular layers only. In the case of polymer films with layer thickness into the p-range, as are usually produced by electropolymerization, account must also be taken of the fact that the charge transport is dependent on both the electron exchange reactions between neighbouring oxidized and reduced sites and the flux of counterions in keeping with the principle of electroneutrality Although the molecular mechanisms of these processes... [Pg.19]

Long Range Charge Transport Through Multistep Hopping. 106... [Pg.78]

Fig. 8 Long range charge transport between dppz complexes of Ru(III) and an artificial base, methyl indole, in DNA. The methyl indole is paired opposite cytosine and separated from the intercalating oxidant by distances up to 37 A. In all assemblies, the rate constant for methyl indole formation was found to be coincident with the diffusion-controlled generation of Ru(III) (> 107 s )> indicating that charge transport is not rate limiting over this distance regime... Fig. 8 Long range charge transport between dppz complexes of Ru(III) and an artificial base, methyl indole, in DNA. The methyl indole is paired opposite cytosine and separated from the intercalating oxidant by distances up to 37 A. In all assemblies, the rate constant for methyl indole formation was found to be coincident with the diffusion-controlled generation of Ru(III) (> 107 s )> indicating that charge transport is not rate limiting over this distance regime...
When the 7r-systerns of two or more double bonds overlap, as in conjugated dienes and polyenes, the 7r-clccIrons will be delocalized. This has chemical consequences, which implies that the range of possible chemical reactions is vastly extended over that of the alkenes. Examples are various pericyclic reactions or charge transport in doped polyacetylenes. A detailed understanding of the electronic structure of polyenes is therefore of utmost importance for development within this field. We will first discuss the structure of dienes and polyenes based on theoretical studies. Thereafter the results from experimental studies are presented and discussed. [Pg.31]

As shown above, the intrinsic fluorescence spectra of proteins as well as coenzyme groups and probes shift within very wide ranges depending on their environment. Since the main contribution to spectral shifts is from relaxational properties of the environment, the analysis of relaxation is the necessary first step in establishing correlations of protein structure with fluorescence spectra. Furthermore, the study of relaxation dynamics is a very important approach to the analysis of the fluctuation rates of the electrostatic field in proteins, which is of importance for the understanding of biocatalytic processes and charge transport. Here we will discuss briefly the most illustrative results obtained by the methods of molecular relaxation spectroscopy. [Pg.95]

In this chapter we will attempt to provide a brief but illustrative description of the various aspects of the research and technology of conducting polymers. To appreciate fully the diverse range of operations that these materials may fulfil, it is crucial to understand their basic properties. Therefore, particular attention will be devoted here to the description of the mechanism of charge transport and to the characteristics of the electrodic processes in electrochemical cells. [Pg.230]

Paddison et al. performed high frequency (4 dielectric relaxation studies, in the Gig ertz range, of hydrated Nafion 117 for the purpose of understanding fundamental mechanisms, for example, water molecule rotation and other possible processes that are involved in charge transport. Pure, bulk, liquid water is known to exhibit a distinct dielectric relaxation in the range 10—100 GHz in the form of an e" versus /peak and a sharp drop in the real part of the dielectric permittivity at high / A network analyzer was used for data acquisition, and measurements were taken in reflection mode. [Pg.330]


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