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Nickel(II) chloride (or just nickel chloride) is the chemical compound NiCl 2. The anhydrous salt is yellow, but the more familiar hydrate NiCl 2 ·6H 2 O is green. Nickel(II) chloride, in various forms, is the most important source of nickel for chemical synthesis. The nickel chlorides are deliquescent, absorbing moisture from the air to form ...
The blue isomer is prepared by treating hydrated nickel chloride with triphenylphosphine in alcohols or glacial acetic acid: [1] NiCl 2 •6H 2 O + 2 PPh 3 → NiCl 2 (PPh 3) 2 + 6 H 2 O. When allowed to crystallise from chlorinated solvents, the tetrahedral isomer converts to the square planar isomer. The square planar form is red and diamagnetic.
Hexaamminenickel chloride is the chemical compound with the formula [Ni(NH 3) 6]Cl 2. It is the chloride salt of the metal ammine complex [Ni(NH 3 ) 6 ] 2+ . The cation features six ammonia (called ammines in coordination chemistry) ligands attached to the nickel (II) ion.
Nickel chloride NiCl 2 is yellow, crystallising in the cadmium chloride structure. It can form a hexahydrate, NiCl 2 ·6H 2 O, a tetrahydrate NiCl 2 ·4H 2 O over 29 °C and a dihydrate, NiCl 2 ·2H 2 O over 64 °C. [3] Ammine complexes like hexaamminenickel chloride also exist. Nickel bromide NiBr 2 is yellow, also crystallising in
The diphosphine serves as a bidentate ligand forming six-membered C 3 P 2 M chelate ring with a natural bite angle of 91°. [1] For example, the complex dichloro(1,3-bis(diphenylphosphino)propane)nickel is prepared by combining equimolar portions of the ligand and nickel(II) chloride hexahydrate.
Chloride is more easily oxidized than nickel(II). This is a typical halogen displacement reaction, where a halogen plus a less active halide makes the less active halogen and the more active halide. Like some other metal difluorides, NiF 2 crystallizes in the rutile structure, which features octahedral Ni centers and planar fluorides. [ 3 ]