Synthesis of Surface-Analogue Square-Planar Tetranuclear Nickel Hydride Clusters and Bonding to μ 4 -NR, -O and -BH Ligands.

Tetranuclear Ni complexes were synthesized with bonding to BH, NR, and O in atypical surface-like geometries. The previously reported electron-deficient cluster [( i Pr3 P)Ni]5 H6 (1) reacts with N-methylmorpholine oxide to give [( i Pr3 P)Ni]4 H4 (μ4 -O) (2), which contains O coordinated in the center of a square-plane arrangement of Ni atoms. Reaction of 1 with benzonitrile gave the square-planar tetranuclear Ni cluster [( i Pr3 P)Ni]4 H4 (μ4 -NCH2 Ph) (3), which contains an imido donor in a square-based-pyramidal geometry. This reaction also gives [( i Pr3 P)Ni(N≡CPh)]3 (4), with bridging benzonitrile ligands. Trimer 4 was independently synthesized from the reaction of Ni(COD)2 , i Pr3 P, and PhC≡N. The addition of dihydrogen to a 1:1 mixture of [( i Pr3 P)2 Ni]2 (N2 ) and ( i Pr3 P)2 NiCl2 yielded [( i Pr3 P)Ni]4 (μ3 -H)4 (μ2 -Cl)2 (5), with a tetrahedral Ni core, in contrast to the square-planar geometries of 2 and 3. The solid-state structure of 5 was determined using both X-ray and neutron diffraction. Reaction of 5 with LiBH4 gave [( i Pr3 P)Ni]4 H4 (μ4 -BH)2 ] (6) via loss of LiCl and H2 .