Electron Transfer in Mixed-Valence [FeIII2FeIIO(O2CCH3)6(3-Cl-py)3]·3-Cl-py: Effects of a Crystallographic Phase Transition and Conversion of Solvate and Ligand Molecules from Statically Disordered to Dynamically Disordered on the Valence Detrapping-Reference-Cited by-同舟云学术

Electron Transfer in Mixed-Valence [FeIII2FeIIO(O2CCH3)6(3-Cl-py)3]·3-Cl-py: Effects of a Crystallographic Phase Transition and Conversion of Solvate and Ligand Molecules from Statically Disordered to Dynamically Disordered on the Valence Detrapping

Published:1997-10-01 Issue:21 Volume:36 Page:4717-4733
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Wu Chi-Cheng¹,Hunt Sheri A.¹,Gantzel Peter K.¹,Gütlich Philipp¹,Hendrickson David N.¹

Affiliation:

1. Department of Chemistry-0358, University of California at San Diego, La Jolla, California 92093-0358, and Institut für Anorganische und Analytische Chemie, Johannes Gutenberg-Universität, D-55099 Mainz, Germany

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic9700314

Reference44 articles.

1. Micromodulation: induction of intramolecular electron transfer by solvate molecule dynamics in the iron acetato oxo methylpyridine mixed-valence complex [Fe3O(O2CCH3)6(3-Me-py)3](solvate)

2. Subtle effects of solvate molecules on the rate of intramolecular electron transfer of mixed-valence complexes in the solid state

3. Lattice-engineered micromodulation of intramolecular electron-transfer rates in trinuclear mixed-valence iron acetate complexes

4. Deuteron NMR study of lattice dynamics affecting the rate of intramolecular electron transfer in the iron acetato oxo pyridine mixed-valence complex [Fe3O(O2CCH3)6(py)3](py)

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