Terminal oxides of late transition and main group metal(loid)s are typically highly basic and intrinsically prone to oligomerization. Their isolation traditionally relied on stabilizing π-interactions with the metal, external Lewis acids, or hydrogen bonding. Here, we present an alternative strategy: enforcing the anti-Van't Hoff/Le Bel configuration by structural constraints. A nearly square-planar germanium center embedded in a tetra-amido macrocyclic ligand (TAML) exhibits enhanced Lewis acidity due to significant LUMO lowering. Double deprotonation of its H₂O adduct affords the first example of a terminal germanium oxido dianion, [GeO]²⁻, which can also be seen as a first-of-its-kind monomeric, molecular germanate. Spectroscopic, crystallographic, and computational (NBO, QTAIM, and ETS-NOCV) analyses reveal a highly polarized, predominantly ionic Ge-O single bond. Reactivity studies identify this terminal oxide as a Brønsted superbase (pKa (THF) ≈ 34), a strong nucleophile, and an efficient O²⁻ transfer agent. The findings highlight the structural constraint as an effective strategy to stabilize terminal M-O species, a structural motif of fundamental importance in bond activation, catalysis, and solid-state superbases.
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Hannibal et al. (2025) studied this question.
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