摘要:
Complex Os(eta(5)-C5H5)(C equivalent to CPh){[eta(2)-CH2=C-(CH3)](PPr2)-Pr-i} (1) reacts with HBF4 center dot OEt2 to give the pi-alkyne derivative [Os(eta(5)-C5H5)(eta(2)-HC=CPh){[eta(2)-CH2= C(CH3)](PPr2)-Pr-i}]BF4 (2), which is transformed to [Os(eta 5-C5H5(1,2-dihydro-2-methylnaphth-2-yldiisopropylphos- phine)]BF4 (3) as a result of the coupling of the alkyne with the isopropenyl substituent of the starting phosphine. The tridentate coordination mode of the dihydronaphthylphosphine in 3 is proved by X-ray diffraction analysis.