Synthese, Struktur und Reaktivität zweikerniger Pentamethyl-Cyclopentadien-Nickelkomplexe mit verbrückenden Butadienliganden
摘要:
[{(eta(5)-Me5Cp)Ni}(2)(mu-eta(2):eta(2)-C4H6)] 3 was obtained from [(eta(5)-Me5Cp)Ni(acac)] 1 and magnesiumbutadiene. The crystal structure of 3 was determined by X-ray diffraction and displays an elongated Ni-Ni bond compared with the Ni-Ni bonded dimer [{(eta(5)-Cp)NiPEt3}(2)] 4 containing an unbridged Ni-Ni bond. Compound 3 contains the butadiene ligand in a nonplanar s-trans arrangement bridging two (eta(5)-Me5Cp)Ni-fragments. In situ NMR experiments show that: (a) reaction of 3 with diphenylethyne gives [{(eta(5)-Me5Cp)Ni}(2)(mu-C2Ph2)] 5 by displacement of butadiene and (b) reaction of 3 with triethylphosphine gives a mixture of [{(eta(5)-Me5CpNi} (mu-eta(3):eta(1)-syn-C4H6)[(eta(5)-Me5Cp)Ni(PEt3)] 9a and [{(eta(5)-Me5Cp)Ni} (mu-eta(3):eta(1)-anti-C4H6)(eta(5)-Me5Cp)Ni(PEt3)] 9b. Compounds 5, 9a and 9b are accessible on a preparative scale via a one pot reaction of 1 with magnesium butadiene in the presence of either tolane, or PEt3. The molecular structure of 9a was determined by X-ray diffraction.