Abstract
A theory for electron transfer rates in polar solvents is developed using an expansion of the density matrix in Liouville space and utilizing the analogy with the problem of nonlinear optical line shapes. The relevant solvent longitudinal time scale which controls the rate and the adiabaticity of electron transfer processes is precisely defined in terms of the solvent dielectric function ε(ω) for an arbitrary non-Debye solvent.
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Dates
Type | When |
---|---|
Created | 23 years, 1 month ago (July 26, 2002, 9:20 a.m.) |
Deposited | 1 year, 6 months ago (Feb. 10, 2024, 2:16 a.m.) |
Indexed | 1 year, 6 months ago (Feb. 10, 2024, 4:44 a.m.) |
Issued | 37 years, 7 months ago (Jan. 15, 1988) |
Published | 37 years, 7 months ago (Jan. 15, 1988) |
Published Print | 37 years, 7 months ago (Jan. 15, 1988) |
@article{Sparpaglione_1988, title={What is the solvent longitudinal time scale controlling electron transfer rates?}, volume={88}, ISSN={1089-7690}, url={http://dx.doi.org/10.1063/1.454219}, DOI={10.1063/1.454219}, number={2}, journal={The Journal of Chemical Physics}, publisher={AIP Publishing}, author={Sparpaglione, Massimo and Mukamel, Shaul}, year={1988}, month=jan, pages={1465–1466} }