579490-55-4

Upstream product

• 579490-58-7 methyl[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 100-44-7 benzyl chloride 
• 108-90-7 chlorobenzene 
• 75-09-2 dichloromethane 
• 579490-52-1 [N(o-C₆H₄PPh₂)2]Li(THF)2 
• 29046-78-4 (1,2-dimethoxyethane)dichloronickel(II) 
• 579490-52-1 [bis(2-diphenylphosphinophenyl)amide]Li(THF)2 

Downstream Products

• 579490-62-3 ethyl[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 579490-71-4 (trimethylsilylmethyl)[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 579490-74-7 phenyl[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 579490-58-7 methyl[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 1046380-19-1 [Ni(P(C₆H₅)2C₆H₄NC₆H₄P(C₆H₅)2)(OC₆H₅)] 
• 1046380-49-7 [Ni(P(C₆H₅)2C₆H₄NC₆H₄P(C₆H₅)2)(OC(CH₃)3)] 
• 1046380-07-7 [Ni(P(C₆H₅)2C₆H₄NC₆H₄P(C₆H₅)2)(NHC₆H₅)] 
• 1046380-45-3 [Ni(P(C₆H₅)2C₆H₄NC₆H₄P(C₆H₅)2)(NHC(CH₃)3)] 
• 1046380-31-7 [Ni(P(C₆H₅)2C₆H₄NC₆H₄P(C₆H₅)2)(SC₆H₅)] 
• 881020-87-7 [N(o-C₆H₄PPh₂)2]Ni(n-hexyl) 
• 881020-84-4 [N(o-C₆H₄PPh₂)2]NiI 
• 579490-65-6 n-butyl[bis(2-diphenylphosphinophenyl)amide]nickel(II) 
• 1034653-33-2 [N(o-C₆H₄PPh₂)2]NiH 

Relevant academic research and scientific papers

Amido pincer complexes of Nickel(II): Synthesis, structure, and reactivity

A series of diamagnetic divalent nickel complexes supported by a tridentate amido diphosphine ligand [N(o-C6H4PR2) 2]- ([R-PNP]-; R = Ph, iPr, Cy) have been prepared and characte

Catalytic carbon-carbon bond formation

The present invention mainly relates to a carbon-carbon bond formation catalyzed by a complex comprising a novel and stable ligand and a metal center. The ligand uses a ring, particularly a phenyl group, or a hydrocarbon group to link an amino group and PR1R2, NR1R2, OR1, SR1, or AsR1R2 group for stabling the structure of the ligand.

Nickel(II) complexes of bis(2-diphenylphosphinophenyl)amide

A series of o-phenylene derivatives were synthesized with an aim to develop new chelating amido phosphine ligands. A monoanionic tridentate bis(2-diphenylphosphinophenyl)amide ligand and its lithium and divalent nickel derivatives were prepared. The coordination chemistry of the synthesized products were studied. The alkyl complexes were found to be highly stable to β-elimination.