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University of Illinois at Urbana-Champaign

Electron Transfer in Oxo-Centered, Trinuclear, Mixed-Valence Iron-Acetate Complexes

Abstract

dc:description

It was found in this study that the three-dimensional packing arrangement in the solid state is the most crucial factor influencing the rate of intramolecular electron transfer in a series of oxo-centered, trinuclear, mixed-valence complexes of the composition Fe(,3)O(O(,2)CH(,3))(,6)(L)(,3) (S), where L is an axial ligand such as pyridine or substituted pyridines and S is a solvate molecule in the solid state lattice.

Degree

thesis:*
Name thesis:degree_name
Ph.D.
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Illinois at Urbana-Champaign
Year dc:date
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Oh, Seung Mo

Subjects

dc:subject × 1

Identifiers

dc:identifier.*
Identifier
(UMI)AAI8623381
OAI identifier oai:identifier
oai:www.ideals.illinois.edu:2142/70332

Chain of custody

source
Harvested from
University of Illinois - Urbana-Champaign
Base URL
www.ideals.illinois.edu/oai-pmh
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Oh, Seung Mo. Electron Transfer in Oxo-Centered, Trinuclear, Mixed-Valence Iron-Acetate Complexes. Dissertation thesis, University of Illinois at Urbana-Champaign, 2014. http://hdl.handle.net/2142/70332