Strongly reducing magnesium(0) complexes

Abstract

A complex of a metal in its zero oxidation state can be considered a stabilized, but highly reactive, form of a single metal atom. Such complexes are common for the more noble transition metals. Although rare examples are known for electronegative late-main-group p-block metals or semimetals^1-6, it is a challenge to isolate early-main-group s-block metals in their zero oxidation state^7-11. This is directly related to their very low electronegativity and strong tendency to oxidize. Here we present examples of zero-oxidation-state magnesium (that is, magnesium(0)) complexes that are stabilized by superbulky, monoanionic, β-diketiminate ligands. Whereas the reactivity of an organomagnesium compound is typically defined by the nucleophilicity of its organic groups and the electrophilicity of Mg²⁺ cations, the Mg⁰ complexes reported here feature electron-rich Mg centres that are nucleophilic and strongly reducing. The latter property is exemplified by the ability to reduce Na⁺ to Na⁰. We also present a complex with a linear Mg₃ core that formally could be described as a Mg^I-Mg⁰-Mg^I unit. Such multinuclear mixed-valence Mg_n clusters are discussed as fleeting intermediates during the early stages of Grignard reagent formation. Their remarkably strong reducing power implies a rich reactivity and application as specialized reducing agents.