Characterization of the Successive One-Electron Oxidation Products of the Dicobalt Fulvalenediyl (Fv) Compound Co2Fv(CO)4 and its Phosphine-Substituted Product
Author:
Affiliation:
1. Department of Chemistry, University of Vermont, Burlington, Vermont 05405
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om800546d
Reference69 articles.
1. References for homodinuclear metal carbonyl complexes are given in refs 2−5. For heterodinuclear examples see:
2. Fulvalenyl Mono- and Diiron Complexes: Photolytic and Electron-Transfer-Induced Substitution of the Benzene Ligands by Phosphines and CO in the Diiron Fulvalenyl Dibenzene Complexes [Fe2Fv(C6H6)2]2+/0. Generation of the Average-Valence Species [Fe2FvL6]3+ (L = Phosphine)
3. Electrochemistry of carbonyl(fulvalene) dimetal complexes of chromium, molybdenum, tungsten, ruthenum, and molybdenum-ruthenium
4. FvCr2(CO)4L2 (Fv = Fulvalene; L = PMe2Ph, PMe3), Metal−Metal-Bonded Compounds Which Undergo Spontaneous Thermal Homolysis to Their Biradical Isomers. Relevant Chemistry of the Compounds FvCr2(CO)4L2X2 (X = H, Cl, Br, I)
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