Solvent Effects on Simple Electron Transfer Reactions. A Comparison of Results in Debye and Non Debye Solvents

Abstract

Estimation of the longitudinal relaxation time for non-Debye solvents is considered on the basis of Hynes' theory for solvents exhibiting more than one relaxation process. It is shown that the major portion of the solvent effect on electron transfer kinetics in these solvents follows that in Debye solvents when the high frequency limiting value is used. The solvent effect on the outer sphere contribution to the Gibbs energy of activation is then examined with respect to the variation in solvent permittivity. Analysis of the available data suggests that the reactants involved in electron transfer are solvated mainly by solvent monomers such that the dielectric constant in the vicinity of the reactant is considerably reduced in protic solvents.

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Document Details

Document Type
Technical Report
Publication Date
May 20, 1991
Accession Number
ADA237157

Entities

People

  • Colby A. Foss Jr.
  • William Ronald Fawcett

Organizations

  • University of California, Davis

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Alcohols
  • California
  • Carbonate Esters
  • Carbonates
  • Chemical Synthesis
  • Chemistry
  • Dielectric Permittivity
  • Dielectric Properties
  • Electrodes
  • Electron Transfer
  • Equations
  • Kinetics
  • Military Research
  • Molecular Orbital Theory
  • Organic Chemistry
  • Relaxation Time
  • Standards

Fields of Study

  • Chemistry

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  • Electrochemical Engineering/ Fuel Cell Technologies
  • Microwave Engineering.

Technology Areas

  • Microelectronics