A neutral cyclic aluminium (I) trimer.

Squire, Imogen; de Vere-Tucker, Matthew; Tritto, Michelangelo; Silva de Moraes, Lygia; Krämer, Tobias; Bakewell, Clare · Nat Commun · 2026

basic_science · Level V

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Abstract

As part of the quest to develop metal-based redox chemistry beyond the d-block, low oxidation state aluminium complexes have gained wide recognition as discrete and versatile 2-electron reductants. Despite reports of monomeric, dimeric and tetrameric neutral structures, as well as a range of charged aluminyl compounds, neutral trimeric structures have remained notably absent. Furthermore, trimeric nuclearity has previously not been considered when investigating reaction mechanisms. Here, we report two neutral Al<sup>I</sup> trimers, cyclotrialumanes. The molecules are extensively characterised using both experimental and computational techniques, with the Al-Al bonds described as principally covalent in nature and the trimeric structure shown to be retained in solution. The cyclotrialumanes are highly reactive, activating a range of small molecules and unsaturated substrates (e.g. H<sub>2</sub>, alkyne, benzene). Most significantly, through a series of extraordinary reactions with ethylene, the cyclotrialumanes are shown to react directly as trimers, forming 5- and 7-membered Al-C ring systems.