Investigations reveal β-diketiminates' reactivity switch to CO2, suggesting ways to design new materials.
Enolate carboxylation by CO₂ is essential to applications ranging from polymer synthesis to CO₂ capture, yet the CO₂ reactivity of stabilized enolates, such as β-dicarbonyl enolates, remains understudied. Combining detailed NMR and DFT studies, we report the reactivity of diverse potassium β-diketonates and β-diketiminates toward CO₂. Our findings reveal the critical role of β'-substituents on β-diketiminates and an unexpected CO₂-concentration-dependent reactivity switch, offering structural insights for designing materials with tunable CO₂ reactivity.
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Meng et al. (2026) studied this question.
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