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Alkylzinc-mediated transmetallation of a calcium hydride.

作者信息

Pearce Kyle G, Mahon Mary F, Hill Michael S

机构信息

Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.

出版信息

Dalton Trans. 2025 Jun 3;54(22):8903-8907. doi: 10.1039/d5dt00958h.

DOI:10.1039/d5dt00958h
PMID:40356461
Abstract

The dimeric β-diketiminato calcium hydride, [(BDI)CaH] (BDI = HC{(Me)CNDipp}; Dipp = 2,6--PrCH), reacts with dialkylzinc reagents in a 1 : 2 ratio through sequential dialkyl(hydrido)zincate formation, calcium alkyl extrusion followed by further irreversible transmetallation of both the organyl and spectator BDI ligands, demonstrating the generality of this transmetallation strategy to access calcium alkyls or ligated zinc alkylated species. When the reaction is performed with dimethyl zinc and an organocalcium dimer with a pre-installed kinetically stabilising aryl substituent, [(BDI)Ca(μ-3,5-BuCH)(μ-H)Ca(BDI)], an organocalcium dimer comprised of differentiated alkyl and aryl functionalities can be accessed through hydride-for-methyl exchange, [(BDI)Ca(μ-3,5-BuCH)(μ-Me)Ca(BDI)].

摘要

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