Tweaking the bridge in metallocene Zr(iv)/W(iv) bimetallic hydrides†
‡a
Alceo
Macchioni,
b
David L.
Hughes,
a
Peter H. M.
Budzelaar
*c
and
Luca
Rocchigiani
*ab
Abstract
Zirconocene cations react with Cp2WH2 affording the bimetallic [Cp2Zr(μ-H)(μ–η1:η5-C5H4)WHCp]+ bridging hydride 1 (Cp = cyclopentadienyl anion, C5H5−) via σ-bond metathesis. Complex 1 features an atypical out of plane Zr(μ-H)W moiety, where no intermetallic interaction is involved, and a fluxional core. Coordination geometry and bond distances of the bridging hydride interaction can be modulated upon reaction with Lewis bases and unsaturated substrates. PMe3, P(p-tol)3, 3,5-dimethylpyridine and THF bind to 1 and shift the hydride bridge on the coordination plane of Zr. Insertion of olefins and alkynes into the Zr–C bond of 1 leads instead to alkyl and vinyl species where the Zr and W coordination planes are perpendicular to each other. Such alterations of the Zr(μ-H)W arrangement are reflected in the average 1H NMR chemical shift values of the hydride, which correlate linearly with computed Zr–H distances. Reactivity experiments with H2 showed that the bridging hydride interaction prevents bimetallic cooperativity and that σ-bond metathesis between Zr–C and H–H bonds is the preferred pathway for all the investigated complexes.
Please wait while we load your content...
