The asymmetric unit of title complex, [Ni(C(20)H(12)BrClN(2)O(2))(C(5)H(5)N)], contains one complex with the central Ni atom in a slightly distorted square-planar environment, formed by the tridentate hydrazone and the monodentate pyridine ligands, with N atoms in a trans arrangement about the Ni atom.

A stable nickel(II) methyl complex containing a diphosphino-boryl (PBP) pincer ligand is described. Mechanistic studies on the hydrogenolysis of the Ni-Me bond suggest a metal ligand cooperation mechanism that involves the intermediacy of a σ-B-H Ni(0) species that further undergoes B-H oxidative addition to form a Ni(II) hydride complex.

The synthesis and reactivity of nickel complexes with the [2-(dimethylamino)ethyl]cyclopentadienyl ligand (CpN) are described. The reaction of NiBr2 with CpNLi leads to the new paramagnetic nickelocene derivative (Cp)2Ni (1), which has been characterized by 1H and 13C NMR, elemental analysis, and mass spectroscopy. Synproportionation of this complex with Ni(CO)4 affords quantitatively the dimer...

[Ni(L(1))Fe((t)BuNC)4](PF6)2 is a robust Ni(II)Fe(II) complex that undergoes a reversible one-electron reduction. Spectroscopic and theoretical studies show that [Ni(L(1))Fe((t)BuNC)4](+) is an unprecedented Ni(I)Fe(II) species that reproduces the electronic configuration of the Ni-L state of the [NiFe] hydrogenases.

A symmetric complex [NiL2(H2O)2]Cl2, where L = 2-picolylamine was synthesized and characterized by spectroscopic and structural methods. Single crystal X-ray studies reveal that the Ni(II) center located in a pseudo-octahedral N4O2 environment with bidentate ligands L positioned in basal and two water molecules in the apical position. The complex is solvatochromic, ionochromic and thermochromic...

In situ electropolymerization as a facile synthetic procedure has been used to obtain highly active compositesof ionic liquid functionalized graphene oxide(FGO)and poly ortho aminophenol (POAP). Surface and electrochemical analysis have been used for characterisation of FGO-POAP composite film. Nickel was accumulated by complex formation between Ni (II) in solution and amines sites in the polym...

In situ electropolymerization as a facile synthetic procedure has been used to obtain highly active compositesof ionic liquid functionalized graphene oxide(FGO)and poly ortho aminophenol (POAP). Surface and electrochemical analysis have been used for characterisation of FGO-POAP composite film. Nickel was accumulated by complex formation between Ni (II) in solution and amines sites in the polym...

We report the first anion photoelectron spectroscopic study of nickel monoxide ~NiO!, nickel dioxide ~ONiO!, and nickel-O2 complex, Ni~O2!. The adiabatic electron affinity ~EA! of NiO is measured to be 1.46 ~2! eV. Five low-lying electronic excited states (A P , a D , B F , b S, c P) are observed for NiO at 0.43 ~4!, 0.94 ~4!, 1.24 ~3!, 1.80 ~10!, and 2.38 ~10! eV above the ground state, respec...

The three-coordinate Ni(I) complex Ni(Cl)(P(2)), where P(2) is the diphosphine (iPr)DPDBFphos, reacts with the acids HCl·(dioxane) and 2,6-lutidinium chloride to generate Ni(H)(Cl)(P(2)) and Ni(Cl)(2)(P(2)). Photolysis of the Ni(H)(X)(P(2)) (for X = Cl, Br) results in formation of H(2) and the Ni(I) halide. This reaction also proceeds in reverse when heated.

The Ni atom at the catalytic center of [NiFe] hydrogenases is incorporated by a Ni-metallochaperone, HypA, and a GTPase/ATPase, HypB. We report the crystal structures of the transient complex formed between HypA and ATPase-type HypB (HypBAT) with Ni ions. Transient association between HypA and HypBAT is controlled by the ATP hydrolysis cycle of HypBAT, which is accelerated by HypA. Only the ATP...