Zirconium Sandwich Complexes with η9 Indenyl Ligands: Well-Defined Precursors for Zirconocene-Mediated Coupling Reactions

Abstract

A family of isolable, well-defined bis-indenyl zirconium sandwich complexes, (eta(5)-C(9)H(5)-1,3-R(2))(eta(9)-C(9)H(5)-1,3-R(2))Zr (R = silyl, alkyl), have been prepared by either alkane reductive elimination or alkali metal reduction of a suitable zirconium(IV) dihalide precursor. Crystallographic characterization of two of these derivatives, R = SiMe(2)CMe(3) and CHMe(2), reveals unprecedented eta(9) coordination of one of the indenyl ligands. Variable-temperature and EXSY NMR studies establish that the eta(5) and eta(9) rings are rapidly interconverting in solution. The sandwich complexes serve as effective sources of low-valent zirconium reacting rapidly with both olefins and alkynes at ambient temperature. In contrast to bis-cyclopentadienyl chemistry, the olefin adducts of the bis-indenyl zirconium sandwiches undergo preferential C-H activation to yield the corresponding allyl hydride compounds, although reaction with excess olefin proceeds through the eta(2)-olefin adduct, forming the corresponding zirconacyclopentane.