Issue 21, 1992

A novel intramolecular metallacycle-phosphine reaction of an electrochemically oxidized cobaltacyclopentadiene complex

Abstract

A ferrocene-substituted cobaltacyclopentadiene complex, C5H5(PPh3)[C[graphic omitted]H](1, Fc = ferrocenyl) undergoes quasi–reversible two-step one-electron oxidation reactions in 0.1 mol dm–3 Bu4NClO4–CH2Cl2 at room temperature, while irreversible two-electro[n with combining macron] oxidation (ECE reaction) of C5H5(PPh3)[C[graphic omitted]Fc]2 causes intramolecular addition of PPh3 fragments to the buta-1,3-dienediyl moiety, affording PhCFc[double bond, length as m-dash]CH–CH[double bond, length as m-dash]CFcPOPh27 and PhCFc[double bond, length as m-dash]CH–CFc[double bond, length as m-dash]CHPPh28.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1553-1555

A novel intramolecular metallacycle-phosphine reaction of an electrochemically oxidized cobaltacyclopentadiene complex

A. Ohkubo, T. Fujita, S. Ohba, K. Aramaki and H. Nishihara, J. Chem. Soc., Chem. Commun., 1992, 1553 DOI: 10.1039/C39920001553

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