Recently Kakitani and Mataga claimed that the free energy dependence of electron transfer rates in polar solvents could be explained by taking into account the dielectric saturation effect of polar solvents. It is shown that the basic assumption of their model is incorrect. The correct treatment of
Dielectric effects in biopolymers: The theory of ionic saturation revisited
β Scribed by B. E. Hingerty; R. H. Ritchie; T. L. Ferrell; J. E. Turner
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1985
- Tongue
- English
- Weight
- 543 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Electrostatic effects are believed to determine the molecular structure and function of macromolecules in many ways. In metallo-based enzymes and in metal-macromolecule interactions in solution, these effects may predominate. In order to tackle metal ion-nucleic acid interactions theoretically, we propose a modification of Debye's distance-dependent dielectric function first proposed more than 50 years ago. This function more closely approximates physical reality a t small interatomic separations. Our theory yields a dielectric function that gives reasonable agreement with experimental data in preliminary calculations.
π SIMILAR VOLUMES
Ah&act-The equation of charge transport, in the absence, of diffusion and convection, but with finite rates of ionic dissociation and recombination taken into account, is developed and solved for a system in which a uniformly charged low dielectric constant fluid is allowed to relax its charge at it