Synthesis, Structure, and Reactivity of Mononuclear Re(I) Oximato Complexes

Complexes [Re(ONCMe2)(CO)3(bipy)] (1) and [Re(ONCMe2)(CO)3(phen)] (2), synthesized by reaction of the respective
triflato precursors [Re(OTf)(CO)3(N−N)] (N−N = bipy, phen) with KONCMe2, feature O-bonded monodentate oximato
ligands. Compound [Re(CO)3(phen)(HONCMe2)]BAr‘4 (3), with a monodentate N-bonded oxime ligand, was prepared
by reaction of [Re(OTf)(CO)3(phen)], HONCMe2, and NaBAr‘4. Deprotonation of 3 afforded 2. The oximato complexes
reacted with p-tolylisocyanate, p-tolylisothiocyanate, maleic anhydride, and tetracyanoethylene, affording the products
of the insertion of the electrophile into the Re−O bond, compounds 4−7. One representative of each type of
compound was fully characterized, including single-crystal X-ray diffraction. The reactions of 1 and 2 with
dimethylacetylenedicarboxylate were found to involve first an insertion as the ones mentioned above but followed
by incorporation of water, loss of acetone, and formation of the charge-separated neutral amido complexes 9 and
10. The structure of 9 and 10 was determined by X-ray diffraction, and key features of their electronic distribution
were studied using a topological analysis of the electron density as obtained from the Fourier map.