One-electron transfer reactions of cyclooctatetraene (cot) complexes: electron spin resonance studies of60CO γ-irradiated [Fe(CO)2L(η4-cot)][L = CO or P(OPh)3]
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1991/DT/DT9910000393
Reference30 articles.
1. N. G. Connelly , in Paramagnetic Organometallic Species in Activation/Selectivity, Catalysis, eds. M. Chanon, M. Julliard and J. C. Poite, Kluwer Academic Publishers, Holland, 1989, p. 71;
2. Synthetic applications of organotransition-metal redox reactions
3. Reduction-oxidation properties of organotransition-metal complexes. Part 12. Formation of carbon–carbon bonds via the oxidative dimerisation of [Fe(CO)3(η4-C8H8)] and the reduction of [Fe2(CO)6(η5:η′5-C16H16)]2+; X-ray crystal structures of [Fe2(CO)4{P(OPh)3}2(η5:η′5-C16H16)][PF6]2and [Fe(CO)3(η4-C16H16)]
4. Reduction–oxidation properties of organotransition-metal complexes. Part 24. The oxidative dimerisation of [Ru(CO)2L(η4-cot)](L = CO or PPh3, cot = cyclo-octatetraene)
5. N. G. Connelly and M.Gilbert, unpublished work.
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1. Mononuclear Iron Compounds with η1–η6 Hydrocarbon Ligands;Comprehensive Organometallic Chemistry II;1995
2. Organoiron chemistry. Annual survey for the year 1991;Journal of Organometallic Chemistry;1993-09
3. Structural consequences of electron-transfer reactions. 25. Electron-transfer-induced isomerizations of cobalt-, nickel-, and palladium-cyclooctatetraene complexes: the role played by the ligand vs. metal composition of the redox orbital;Journal of the American Chemical Society;1993-03
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