A Terminal Ni(III)−Imide with Diverse Reactivity Pathways

Journal of the American Chemical Society2005Vol. 127(32), pp. 11248–11249

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E. Kogut, Heather L. Wiencko, Libei Zhang, D.E. Cordeau, Timothy H. Warren

Abstract

The synthesis and structure of the β-diketiminato Ni(I) lutidine adducts [MexNN]Ni(2,4-lutidine) (x = 2 (2); x = 3 (3)) are described which serve as synthons to the “naked” 13-electron [MexNN]Ni fragments in reactions with N3Ad to give Ni−imido complexes. The singly bridged imide {[Me2NN]Ni}2(μ-NAd) (4) possesses short Ni−Ni (2.506(1) Å) and Ni−N(imido) distances (1.732(4)−1.752(4) Å). Steric modification of the β-diketiminate ligand to include an additional methyl group in the N-aryl 4-position affords the Ni(III) terminal imide [Me3NN]NiNAd (8) isolated in 52% yield. The X-ray structure of terminal imide 8 reveals a contracted Ni−N(imido) bond distance (1.662(2) Å) and an only somewhat bent imido linkage (Ni−N−C = 164.5(2)°) consistent with a significant degree of multiple bond character. Frozen glass EPR studies of 5 indicate a rhombic environment in which one of the signals exhibits strong hyperfine coupling (A = 22 G) to the imido 14N (I = 1) nucleus. The terminal imide 5 undergoes complete imido group transfer to CO and CNBut to give AdNCO and AdNCNBut, respectively, as well as with PMe3 to afford AdNPMe3. Exemplifying the radical character at the imido N atom, 5 adds to cobaltocene and abstracts a H atom from 1,4-cyclohexadiene to give the Ni(II)−amides [Me3NN]Ni−NAd(η4-C5H5)CoCp (7) and [Me3NN]Ni−NHAd (8).

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Abstract

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