(η-C5H5)(OC)Feη3-CH2C(Me)C[OC(O)Ph](Me) and (η-C5H5)(OC)Feη3-CH2C(OMe)C[OC(O)Ph](Me) are isolated in 8 and 11% yield, respectively. These η3-allyl ligands are presumably formed via CC coupling of the donor atoms of the formal acyl and alkenyl ligands in the intermediate complexes.
当ferraenolate阴离子,(η-C 5 H ^ 5)(CO)2 F
EC(O)CH 2 -中,依次用
甲基锂/ TME
DA和
苯甲酰氯,已知η处理3 -烯丙基配合物,(η-C 5 H ^ 5)(OC)的Fe η 3 -CH 2 C [OC(O)PH] C [OC(O)PH](CH 3 },分离产率为36%。当该中性烯络合物,(η-C 5 ħ 5)(CO)2的Fe [C(Me)的CH 2 ]和(η-C 5 H ^ 5)(OC)2的Fe C(OME)CH 2]中,用甲基和
苯甲酰氯依次处理时,η 3 -烯丙基配合物,(η-C 5 H ^ 5)(OC)的Fe η 3 -CH 2 C(Me)的C [OC(O)PH](ME )和(η-C 5 H ^ 5)(OC)的Fe η 3 -CH 2 C(OME)C [OC(O)PH](Me)中分别分离在8和11%的产率,。这些η 3 -烯丙基
配体经由C