Solution Chemistry and Reactivity of Tris(N,N-dialkyldithiocarbamato)-oxomolybdenum(VI) Cationic Complexes

DOI: 10.1039/DT9830002135

Source and publish data:

Journal of the Chemical Society, Dalton Transactions p. 2135 - 2138 (1983)

Update date:2022-09-26

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Authors:

Young, Charles G.

Broomhead, John A.

Boreham, Christopher J.

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Article abstract of DOI:10.1039/DT9830002135

The preparation of the orange diamagnetic compounds X (R = Me or Et, X = BF4(1-), PF6(1-), or ClO4(1-); R = i-Pr, X = BF4(1-)) from the reaction of cis- complexes and HX in acetone is described.Details of the (1)H and (13)C-<(1)H> n.m.r., i.r., and electronic spectra of the complexes are presented.The monomeric complex cations possess a rigid pentagonal-bipyramidal geometry in solution at room temperature.The complex (1+) catalytically converts PPh3 into OPPh3 an air, gives (1+) with PhNCO, undergoes replacement of one S2CNEt2(1-) ligand with Cl(1-) and S2(2-), and yields upon reduction.

Full text of DOI:10.1039/DT9830002135

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