Nickel NiCl2

Dichloro[bis(l,2-diphenylphosphino)ethane]nickel, NiCl2(dppe). 

Sodium/nickel NiCl2 Na Solid 2Na + NiCl2 0 2NaCl + Ni 2.6 719 90-100... 

Nickel forms yellow anhydrous halides NiXjlX = F. Cl. Br) and a black iodide Nil2 all these halides are made by direct combination of the elements, and the chloride by reaction of sulphur dichloride oxide with the hydrated salt. All dissolve in water to give green solutions from which the hydrates can be crystallised the solutions contain the ion [NifHjOls], and the chloride crystallises as NiCl2.6H2O, nickel(II) chloride hexahydrate. 

Nickel Double Salts. Nickel ammonium chloride [16122-03-5], NiCl2 NH Cl -6H20, nickel ammonium sulfate [15699-18-0],... 

Nickel sulphate Nickel chloride (NiCl2-.6H20) 40-60g/l Boric acid (HjBOj) 25-40 g/1... 

This reaction, like that between Zn and Cu2+, can serve as a source of electrical energy in a voltaic cell The cell is similar to that shown in Figure 18.2 except that, in the anode compartment, a nickel electrode is surrounded by a solution of a nickel(II) salt, such as NiCl2 or NiS04. The cell notation is Ni Ni2+ Cu2+ Cu. 

Nickel Chloride NiCl2 [41] and the NiCl2-NaCl System... 

C19-0128. A galvanic cell is constructed using a silver wire coated with silver chloride and a nickel wire immersed in a beaker containing 1.50 X 10 M NiCl2 (a) Determine the balanced cell reaction, (b) Calculate the potential of the cell, (c) Draw a sketch showing the electron transfer reaction occurring at each electrode. 

Reduction of Ni11 chloride complexes [NiCl2(L)] (L = various diphosphinomethanes, -ethanes, and -propanes) with, for example, potassium naphthalenide in THF gives the corresponding Ni1 chlorides [NiCl(L)].2368 By treatment of (963) with LiNHAr, a terminal amido complex of Ni1 (964) was prepared (Scheme 13).2369 It contains planar three-coordinate nickel and a planar amido ligand with d(Ni—N) = 1.881(2) A. The P,Ni,P and C,N,H planes are orthogonal with a 91° dihedral angle. 

Nickel(0) complexes with water-soluble phosphines have attracted interest in the context of homogeneous catalysis. A comprehensive study of the coordination chemistry of tris(sodium-m-sulfonatophenyl)phosphine (1039) has appeared.2504 The complexes [Ni(CO)2(1039)2] 6HzO have been made by reaction of (1039) with Ni(CO)4 under phase-transfer conditions, and the homo-leptic [Ni(1039)3]-9H2O has been made from Ni° precursors and (1039) under phase-transfer conditions, or from NiCl2, (1039), and BH4 in water. A related complex [Ni(CO)2(1040)2] with the bidentate ligand (1040) has also been studied.2505... 

Nickel complexes prove to be the most effective catalysts for hydroboration of thioalkynes. The bidentate phosphine systems [(P-P)NiCl2] (P-P = dppf, l,3-bis(diphenylphosphino)propane(dppp), dppe) all displayed high activity, even with bulky substituents on the alkyne (Equation (4)) 43 44... 

Although more hydrolytically sensitive than the phosphine boranes, diorganochlorophosphines can be more accessible than diorganophosphines and are not pyrophoric. Thus, the reaction of a chlorophosphine with an aryl halide or aryl triflate in the presence of zinc as a reducing agent and (DPPE)NiCl2 as catalyst provides a convenient procedure for P—C coupling (Equation (49)).150 A related nickel-catalyzed process driven by electrochemical reduction has also been reported 151... 

The feasibility of carbon-supported nickel-based catalysts as the alternative to the platinum catalyst is studied in this chapter. Carbon-supported nickel (Ni/C, 10 wt-metal% [12]), ruthenium (Ru/C, 10 wt-metal% [12]), and nickel-ruthenium composite (Ni-Ru/C, 10 wt-metal%, mixed molar ratio of Ni/Ru 0.25,1,4, 8, and 16 [12]) catalysts were prepared similarly by the impregnation method. Granular powders of the activated carbon without the base pretreatment were stirred with the NiCl2, RuC13, and NiCl2-RuCl3 aqueous solutions at room temperature for 24 h, respectively. Reduction and washing were carried out in the same way as done for the Pt/C catalyst. Finally, these nickel-based catalysts were evacuated at 70°C for 10 h. 

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