738588-96-0

Upstream product

• 14264-16-5 bis(triphenylphosphine)nickel(II) chloride 
• 7647-01-0 hydrogenchloride 
• 220135-31-9 ((CH₃)3C)2PC₂H₄P(C(CH₃)3)2NiICD₃ 
• 219938-27-9 (1-methylindenyl)Ni(PPh₃)2(succinimidate) 
• 219938-26-8 (1-methylindenyl)Ni(PPh₃)2(maleimidate) 
• 219938-24-6 (1-methylindenyl)Ni(PPh₃)2(4,5-dichlorophtalimidate) 

Downstream Products

• 219938-27-9 (1-methylindenyl)Ni(PPh₃)2(succinimidate) 
• 186262-52-2 (η(3)-1-Me-indenyl)Ni(PPh3)(Me) 
• 219938-23-5 (1-methylindenyl)Ni(PPh₃)2(phtalimidate) 
• 196408-68-1 (CH₃C₉H₆)Ni(P(C₆H₅)3)2⁽¹⁺⁾ 
• 500362-65-2 [(1-methylindenyl)Ni(PPh₃)(thienyl)] 
• 196408-69-2 (C₉H₆CH₃)Ni(P(C₆H₅)3)2⁽¹⁺⁾*BF₄^(1-)=[(C₉H₆CH₃)Ni(P(C₆H₅)3)2]BF₄ 
• 196408-72-7 (C₉H₆CH₃)Ni(P(C₆H₅)3)(CH₃CN)⁽¹⁺⁾*BF₄^(1-)=[(C₉H₆CH₃)Ni(P(C₆H₅)3)(CH₃CN)]BF₄ 
• 255736-79-9 (1-Me-Ind)Ni(PPh₃)(CC-Ph) 
• 219938-24-6 (1-methylindenyl)Ni(PPh₃)2(4,5-dichlorophtalimidate) 

Relevant academic research and scientific papers

Indenylnickel imidato complexes: Synthesis, characterization, and reactivities

The complex (1-Me-indenyl)Ni(PPh3)(phthalimidate) has been prepared and fully characterized by IR and 1H, 13C{1H}, and 31P{1H} NMR spectroscopy and single-crystal X-ray diffraction. The ana

Structural and NMR studies of indenyl hapticity and rotational barriers in the complexes (η-1-R-indenyl)Ni(PPh3)(X) (R = H, Me; X = Cl, Me)

The relative trans influences of Cl and Me in the complexes (1-Me-indenyl)Ni(PPh3)Cl and (1-Me-indenyl)Ni(PPh3)Me lead to different solid state hapticities for the 1-Me-indenyl ligands. Comparing the solution NMR data for these compl