Summary
The synthesis and properties of the [(η5-C5H5)L(RN3R)CoIII]PF6 complexes, with L = PEt3, PPh3, P(OMe)3 or P(OPh)3, are reported. A six coordinate configuration containing a chelating triazenido ligand is proposed which is isostructural with the known complexes of iron and nickel.
The spectroscopic properties of the isoelectronic Co and Fe complexes, (η5-C5H5)L(RN3R)M, are compared in relation to the charge on the central metal atom. The complex with L = CO could not be prepared, but the carbonyl inserted product (η5-C5H5)(L{RNNN(R)C(O)}Co was isolated. In one of the reactions, the novel ring-bound triphenylphosphine complex, [η5-C5H5)(η5-C5H4PPh3)CoIII](PF6)2, was isolated as a side product. The mechanism of this reaction is discussed.
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A stable cobalt hydride could be isolated in the Me related reaction, [η5-C5H5)(PRt3)2Co](BF4)2 + PEt3→ [(η5-C5H4PEt3)(PEt3)2HCo](BF4)2, R. J. McKinney, private communication.
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Pfeiffer, E., Kokkes, M.W. & Vrieze, K. Isostructural triazenido complexes of first row transition metals. Part 2. Synthesis and properties of [(η5-C5H5)L(RN3R)CoIII]PF6, L = PEt3, PPh3, P(OMe)3 and P(OPh)3 . Transition Met Chem 4, 389–393 (1979). https://doi.org/10.1007/BF00623985
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DOI: https://doi.org/10.1007/BF00623985