Tweaking the bridge in metallocene Zr(IV)/W(IV) bimetallic hydrides.

Autor: Fernando S; School of Chemistry, University of East Anglia, Norwich Research Park, NR47TJ, Norwich, UK., Landrini M; Department of Chemistry, Biology and Biotechnology and CIRCC, University of Perugia, I-06123, Perugia, Italy. luca.rocchigiani@unipg.it., Macchioni A; Department of Chemistry, Biology and Biotechnology and CIRCC, University of Perugia, I-06123, Perugia, Italy. luca.rocchigiani@unipg.it., Hughes DL; School of Chemistry, University of East Anglia, Norwich Research Park, NR47TJ, Norwich, UK., Budzelaar PHM; Department of Chemistry, University of Naples Federico II, Via Cintia, I-80126, Naples, Italy. p.budzelaar@unina.it., Rocchigiani L; School of Chemistry, University of East Anglia, Norwich Research Park, NR47TJ, Norwich, UK.; Department of Chemistry, Biology and Biotechnology and CIRCC, University of Perugia, I-06123, Perugia, Italy. luca.rocchigiani@unipg.it.
Jazyk: angličtina
Zdroj: Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2023 Jan 03; Vol. 52 (2), pp. 394-408. Date of Electronic Publication: 2023 Jan 03.
DOI: 10.1039/d2dt03833a
Abstrakt: Zirconocene cations react with Cp 2 WH 2 affording the bimetallic [Cp 2 Zr(μ-H)(μ-η 15 -C 5 H 4 )WHCp] + bridging hydride 1 (Cp = cyclopentadienyl anion, C 5 H 5 - ) 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. PMe 3 , 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 1 H NMR chemical shift values of the hydride, which correlate linearly with computed Zr-H distances. Reactivity experiments with H 2 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.
Databáze: MEDLINE