Highly monodisperse 5 nm Pd-Ni alloy nanoparticles (NPs) were prepared by the reduction of Pd(acac)(2)/Ni(acac)(2) mixtures with tert-butylamine-borane complex (TBAB) in the presence of oleic acid (OA) and oleylamine (OAm). Employing TBAB as an effective reductant and OA/OAm combination as an effective stabilizing agent is crucial to the formation of monodisperse Pd-Ni NPs. Experimental results...

The title compound, [Ni(H(2)O)(6)][Ni(3)(C(7)H(3)NO(4))(4)(H(2)O)(4)]·8H(2)O, was obtained by the reaction of nickel(II) nitrate hexa-hydrate with pyridine-2,6-dicarb-oxy-lic acid (pydcH(2)) and 1,10-phenanothroline (phen) in an aqueous solution. The latter ligand is not involved in formation of the title complex. There are three different Ni(II) atoms in the asymmetric unit, two of which are l...

The title compound, (C(2)H(10)N(2))[Ni(C(16)H(14)N(2)O(2))](4)(ClO(4))(2)·C(3)H(7)NO, crystallizes with four Ni(salen) mol-ecules {salen is 2,2'-[ethane-1,2-diylbis(nitrilo-methyl-idyne)]diphenolate}, one ethyl-enediammonium cation (actually two half-cations, each located on a center of inversion), two perchlorate anions and one dimethyl-formamide solvent mol-ecule in the asymmetric unit. Each ...

Quasielastic neutron scattering experiments were performed with Na-hectorite, Ni-hectorite, and Sm-hectorite samples in order to find out whether Sm is present in the clay interlayer as a fully hydrated cation (outer-sphere complex), or, as it follows from neutron diffraction data analysis, it is dehydrated and bound to the clay surface (inner-sphere complex). The results obtained for the Sm-he...

Reaction of the deprotonated N-thiophosphorylated thiourea 2-PyNHC(S)NHP(S)(OiPr)2 (HL) with NiCl2 leads to the complex [Ni{2-PyNHC(S)NP(S)(OiPr)2}2] ([NiL2]) with unprecedented 1,5,7-N,N′,S-coordination of the ligand. Recrystallization of [NiL2] from a mixture of CH2Cl2–n-hexane or acetone–n-hexane leads to [Ni(L-1,5,7-N,N′,S)2]·CH2Cl2 and [Ni(L-1,5,7-N,N′,S)2], respectively. The latter comple...

An X-ray absorption spectroscopic study of structural changes occurring at the Ni site of Chromatium vinosum hydrogenase during reductive activation, CO binding, and photolysis is presented. Structural details of the Ni sites for the ready silent intermediate state, SI(r), and the carbon monoxide complex, SI-CO, are presented for the first time in any hydrogenase. Analysis of nickel K-edge ener...

The novel dimethyl sulfoxide (DMSO)-coordinated complex [(N,O)Ni(CH(3))(DMSO)] {1-DMSO; (N,O) = kappa(2)-N,O-(2,6-(3,5-(F(3)C)(2)C(6)H(3))(2)C(6)H(3))-N=CH-(3,5-I(2)-2-OC(6)H(2))} was found to be a well-defined, very reactive precursor that enables direct observation of the activation and deactivation of neutral Ni(II) catalysts. Preparative reaction with ethylene afforded the ethyl complex [(N...

Vanadium (III) gives a greenish- yellow complex with anthranilic acid in presence of pyridine. The complex is extractable with chloroform and is used for photometric determination of vanadium by measuring the absorbance at 390 nm against a reagent blank. Beer's Law holds good in the range of 1-20 pg V/ml. Moderate amounts of Pb (II) , Ca (II) , Sr (II) , Ba (II) , Cd (II) , Mg (II) , Mn (II...

A novel asymmetric phenol-based 'end-off' dinucleating ligand 2-{[(2-piperidylmethyl)amino]methyl}-4-bromo-6-[(1-methylhomopiperazine-4-yl)methyl]phenol (HL) and three dinuclear nickel(II) complexes, [Ni₂L(μ-OH)] (ClO₄)₂ (1), [Ni₂L(DNBA)₂(CH₃CN)₂]BPh₄ (2) and [Ni₂L(BPP)₂(CH₃CN)₂]BPh₄ (3) have been synthesized and characterized by a variety of techniques including: NMR, infrared and UV-vis spect...

Two radical-containing Ni(II) complexes having either parent salicylidene (complex 1) or 3,5-di-tert-butylsalicylidene (complex 2) in the ligand backbone were synthesized. Complex 2 underwent ligand centered C–H activation by aerial oxygen, forming the corresponding amide complex (2a). The UV-Vis/NIR spectral changes upon purging of molecular oxygen to 2 in CH2Cl2, alongwith ESI-MS analysis ind...