Nickel alkynyl and allenylidene complexes: Synthesis and properties

Copper-catalyzed reaction of [Cp(PPh3)NiCl] with the terminal alkynes H–Ctriple bond; length of mdashC–C(double bond; length as m-dashO)R (R = O-Menthyl, NMe2, Ph) yields the alkynyl complexes [Cp(PPh3)Ni–Ctriple bond; length of mdashC–C(double bond; length as m-dashO)R]. Subsequent O-methylation with either [Me3O]BF4 or MeSO3CF3 affords cationic allenylidene complexes, [Cp(PPh3)Nidouble bond; length as m-dashCdouble bond; length as m-dashCdouble bond; length as m-dashC(OMe)R]+X¯ (X = BF4, SO3CF3). N-Alkylation of Cp(PPh3)Ni-pyridylethynyl complexes likewise gives cationic allenylidene complexes. [Cp(PPh3)Ni–Ctriple bond; length of mdashC–C(CH)4N] adds BF3 at nitrogen. Modification of the ligand sphere in these nickel allenylidene complexes is possible by replacing PPh3 by PMe3 in the alkynyl complex precursors. The first allenylidene(carbene)nickel cation, [Cp(SIMes)Ndouble bond; length as m-dashCdouble bond; length as m-dashCdouble bond; length as m-dashC(OMe)NMe2]+, is accessible by successive reaction of [Cp(SIMes)NiCl] with H–Ctriple bond; length of mdashC–C(double bond; length as m-dashO)NMe2 and [Me3O]BF4. By the analogous sequence an allenylidene complex containing the chelating (diphenylphosphanyl)ethylcyclopentadienyl ligand can be prepared. DFT Calculations were carried out on the allenylidene complex cation [Cp(PPh3)Nidouble bond; length as m-dashCdouble bond; length as m-dashCdouble bond; length as m-dashC(OMe)NMe2]+ and on its precursor, the alkynyl complex [Cp(PPh3)Ni–Ctriple bond; length of mdashC–C(double bond; length as m-dashO)NMe2]. Based on the spectroscopic data and a X-ray structure analysis the bonding in the new nickel allenylidene complexes is best represented by several resonance forms, an alkynyl resonance form considerably contributing to the overall bond.