Protolysis of Seven-Membered Zirconacyclocumulene Complexes of ZirconoceneстатьяИсследовательская статья
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Аннотация:The interaction of the seven-membered zirconacyclocumulene complex Cp2Zr[η4-Me3SiC4(SiMe3)−C(C2SiMe3)=CSiMe3] (1) with an equimolar amount of HCl in dioxane at 20 °C results in the formation of the complex Cp2Zr(Cl)−C(CCSiMe3)C(SiMe3)−C(CCSiMe3)=CH(SiMe3) (4), wherein one of the CC groups iscoordinated with the Zr atom. Under similar conditions, the reaction of 1 with an excess of HCl affords Cp2ZrCl2 and a mixture cis,cis- and cis,transunsaturated compounds H(Me3Si)CC(C2SiMe3)−C(SiMe3)CH-(C2SiMe3) (5) and H(Me3Si)CC(C2SiMe3)−C(SiMe3)C(H)-C2SiMe3 (6). The isomeric seven-membered zirconacyclocumulene Cp2Zr[η4-Me3SiC4(SiMe3)−C(SiMe3)C(C2SiMe3)] (2) reacts with 2 equiv of HCl in dioxane to give Cp2ZrCl2, H(Me3SiC2)CC(SiMe3)−C(SiMe3)C(C2SiMe3)H (7), and H(Me3SiC2)CC(SiMe3)−C-(SiMe3)CCC(SiMe3)H (8). The subsequent reaction of this mixture with Mg in THF yields zirconabicycles 9 and 10, respectively, containing fused zirconacyclopentadiene and cyclohexadiene rings, and, correspondingly, zirconacyclopentene and cyclopentadiene cycles. From the interaction of 7 with Cp*2ZrCl2 and Mg in THF, complex 11, analogous to 9, was isolated. The protolysis of the seven-membered zirconacyclocumulene Cp2Zr[η4-PhC4(Ph)−(o-C6H4)] (3) with 2 equiv of HCl yields Cp2ZrCl2 and Ph2CC(H)−CCPh (16). The structures of 4, 7, 10, and 11 have been established by X-ray crystallography. The mechanisms of the reactions found are discussed.