Issue 3, 1980

Electroreduction of linear trimetallic complexes: M–Hg–M, (M–Au–M), M–PtL2–M [M = Co(CO)4, Fe(CO)3NO, Mn(CO)5, Cr(CO)3(η-C5H5), Mo(CO)3(η-C5H5), or W(CO)3(η-C5H5); L = ButNC or C6H11NC]; unexpected generation of radicals

Abstract

Cathodic reduction of PtII isocyanide compounds M–PtIIL2–M on platinum and gold electrodes in an aprotic medium leads to unexpected paramagnetic PtI species, whereas under the same conditions M–Hg–M and (M–Au–M) exhibit predictable metal–metal bond cleavage.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1980, 77-78

Electroreduction of linear trimetallic complexes: M–Hg–M, (M–Au–M), M–PtL2–M [M = Co(CO)4, Fe(CO)3NO, Mn(CO)5, Cr(CO)3(η-C5H5), Mo(CO)3(η-C5H5), or W(CO)3(η-C5H5); L = ButNC or C6H11NC]; unexpected generation of radicals

P. Lemoine, A. Giraudeau, M. Gross and P. Braunstein, J. Chem. Soc., Chem. Commun., 1980, 77 DOI: 10.1039/C39800000077

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