Probing the molecular basis of solvent reorganization in electron-transfer reactions

Robert L. Blackbourn, Joseph T Hupp

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

Optical electron transfer in the mixed-valence dimer [(NH3)5RuII-4,4′-bpy-Ru III(NH3)5]5+ has been investigated in mixed solvents (acetonitrile + dimethyl sulfoxide) in order to probe molecular aspects of solvent reorganization. The basis for extracting information at the molecular level lies in the phenomenon of selective solvation and the resulting ability to vary the composition of the dimer's primary solvation layer largely independently of the predominant bulk solvent composition. This enables one to probe the first molecular layer of solvent separately from the rest. From the optical electron-transfer data, corrected for unsymmetrical selective solvation effects, we find that nearly all of the solvent reorganizational energy originates from reorientations occurring within the first molecular solvent layer. The reorganization energy per solvent molecule is fairly large in the first layer (ca. 125-150 cm-1), indicating extreme librational (or other) excitation. Somewhat surprisingly, the molecular picture which emerges from our work is broadly consistent with the predictions of a simple solvent dielectric continuum theory.

Original languageEnglish
Pages (from-to)2817-2820
Number of pages4
JournalJournal of Physical Chemistry
Volume92
Issue number10
Publication statusPublished - 1988

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electron transfer
Electrons
Solvation
solvation
Dimers
dimers
Molecular Probes
Dimethyl sulfoxide
probes
Data transfer
Dimethyl Sulfoxide
Acetonitrile
Chemical analysis
retraining
acetonitrile
continuums
valence
Molecules
energy
predictions

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Probing the molecular basis of solvent reorganization in electron-transfer reactions. / Blackbourn, Robert L.; Hupp, Joseph T.

In: Journal of Physical Chemistry, Vol. 92, No. 10, 1988, p. 2817-2820.

Research output: Contribution to journalArticle

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