Versatile Coordination and C–C Coupling of Diphosphine-Tethered Imine Ligands with Ni(II) and Ni(0)

[Image: see text] Ligands that can adapt their coordination mode to the electronic properties of a metal center are of interest to support catalysis or small molecule activation processes. In this context, the ability of imine moieties to bind in either an η(1)(N)-fashion via σ-donation of the lone pair or, less commonly, in an η(2)(C,N)-fashion via π-coordination is potentially attractive for the design of new metal–ligand cooperative systems. Herein, the coordination chemistry of chelating ligands with a diphosphine imine framework (PCNP) to nickel is investigated. The imine moiety binds in an η(1)(N)-fashion in a Ni(II)Cl(2) complex. The uncommon η(2)(C,N)-interaction is obtained in Ni(0) complexes in the presence of a PPh(3) coligand. Increasing the bulk on the phosphine side-arms in the Ni(0) complexes, by substituting phenyl for o-tolyl groups, leads to a distinct binding mode in which only one of the phosphorus atoms is coordinated. In the absence of a coligand, a mixture of two different dimeric Ni(0) complexes is formed. In one of them, the imine adopts an uncommon η(1)(N)η(2)(C,N) bridging mode of the ligand to nickel, while the second one may involve reactivity on the ligand by the formation of a new C–C bond by oxidative coupling. The latter is supported by the isolation and structural characterization of a crystalline bis-CO derivative featuring a C–C bond formed by oxidative coupling of two imine moieties.