Reactions of a m-terphenylhydridostannylene with β-diketiminato magnesium and calcium hydrides provide bis-μ2-hydrido species, the heterobimetallic constitutions of which are maintained after the addition of THF donor solvent. In both cases, reactions with hex-1-ene result in the formation of tetravalent organostannyl alkaline earth derivatives. Whereas the magnesium reagent undergoes facile twofold addition, the calcium-centered process is arrested after a single alkene reduction event. This contrasting behavior is assessed to result from the heavier alkaline earth element's ability to form a persistent polyhapto interaction with an arene substituent of the m-terphenyl ligand.
Keywords: Calcium; Density functional theory; Hydride; Magnesium; Stannylene.
© 2024 The Author(s). Chemistry - A European Journal published by Wiley-VCH GmbH.