摘要:
Imido complexes of the late transition metals have the ability to activate C-H bonds through the abstraction of hydrogen atoms from hydrocarbons. This paper describes the apparent hydrogen atom transfer from cyclopentadiene (CpH) to the isolable imidoiron(III) complex L(Me)FeNAd (L(Me) = 2,4-bis(2,6-diisopropylphenylimido)pent-3-yl; Ad = 1-adamantyl) in the presence of 4-tert-butylpyridine ((t)Bupy). The isolated product is not the amidoiron(II) complex, but instead it is L(Me)Fe(Cp)((t)Bupy), the result of amido protonation by additional CpH. The crystal structures of both L(Me)FeCp and L(Me)Fe(Cp)((t)Bupy) are presented, and in the latter compound the Fe-C bonds are longer than in any previously characterized cyclopentadienyliron complex. (C) 2010 Elsevier B.V. All rights reserved.