1997 Fiscal Year Final Research Report Summary
Electron Transfer Chemistry of Organometallic Porphyrins
Project/Area Number |
08044083
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Research Category |
Grant-in-Aid for international Scientific Research
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Allocation Type | Single-year Grants |
Section | Joint Research |
Research Field |
物質変換
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Research Institution | Osaka University |
Principal Investigator |
FUKUZUMI Shunichi Osaka University, Faculty of Engineering, Professor, 工学部, 教授 (40144430)
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Co-Investigator(Kenkyū-buntansha) |
KADISH Karl M. University of Houston, Department of Chemistry, Professor, 化学科, 教授
SUENOBU Tomoyoshi Osaka University, Faculty of Engineering, Research Associate, 工学部, 助手 (90271030)
ITOH Shinobu Osaka University, Faculty of Engineering, Associate Professor, 工学部, 助教授 (30184659)
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Project Period (FY) |
1996 – 1997
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Keywords | Organometallics / Porphyrin / Electron Transfer / Redox Potential / Migration Reaction / Oxidation / ESR / Axial Ligand Coordination |
Research Abstract |
The one-electron oxidation of alkyl and aryl metal sigma-bonded porphyrins is often followed by a metal to nitrogen migration of the sigma-bonded organic ligand. Several studies of oxidized cobalt sigma-bonded porphyrins have suggested that a Co^<III> pi cation radical rather than a Co^<IV> cation is generated prior to the migration. The present study combines the use of electrochemistry, UV-vis and ESR spectroscopy and stopped flow kinetics to investigate the reactions and properties of singly oxidized organoporphyrins of the type (P) M (R) and (P) M (R)(L) where P = the dianion of substituted porphyrins : TPP or OEP,M = Co or Fe, R = n-Bu, Et, Me or Ph, L = acetonitrile or a substituted pyridine. The results of our studies show clearly that a (TPP) Co^<IV> (R) complex can be generated under specific solution conditions and the cleavage of the cobalt-carbon bond occurs via a rate-determining intramolecular electron transfer from R to Co and this results in a metal to nitrogen migration of the R group. In a similar mannar, one-electron oxidation of an aryl sigma-bonded iron porphyrin, (OEP) Fe^<III> (R) results in the formation of an Fe^<IV> center which is invariably generated prior to migration.
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[Publications] Shunichi Fukuzumi et al.: "Kinetic and Thermodynamic Studies of Iron(III) and Iron(IV) Sigma Bonded Porphyrins.Formation and Reactivity of[(OEP)Fe(R)]^<n+> where OEP is the Dianion of Octaethylporphyrin,n=0,1,2,3 and R=C_6H_5,3,4,5-C_6F_3H_2,2,4,6-C_6F_3H_2,_6F_4HorC_6F_5" Inorg.Chem.(印刷中). (1998)
Description
「研究成果報告書概要(和文)」より
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[Publications] Shunichi Fukuzumi et al.: "Kinetic and Thermodynamic Studies of Iron (III) and Iron (IV) Sigma Bonded Porphyrins. Formation and Reactivity of [(OEP)Fe(R)]^<n+> where OEP is the Dianion of Octaethylporphyrin, n = 0, l, 2,3 and R = C_6H_5,3,4,5-C_6F_3H_2,2,4,6-C_6F_3H_2, C_6F_4H or C_6F_5" Inorg.Chem. (in press). (1998)
Description
「研究成果報告書概要(欧文)」より
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