Interrogating the Carboxylation of Potassium β-Diketonates and β-Diketiminates by Carbon Dioxide
Enolate carboxylation by CO<sub>2</sub> is essential to applications ranging from polymer synthesis to CO<sub>2</sub> capture, yet the CO<sub>2</sub> 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 CO<sub>2</sub>. Our findings reveal the critical role of β'-substituents on β-diketiminates and an unexpected CO<sub>2</sub>-concentration-dependent reactivity switch, offering structural insights for designing materials with tunable CO<sub>2</sub> reactivity.
Authors
- Phillip J. Milner (ORCID: https://orcid.org/0000-0002-2618-013X)
- Tristan H. Lambert (ORCID: https://orcid.org/0000-0002-7720-3290)
- Ivan Keresztes (ORCID: https://orcid.org/0000-0002-1271-3847)
- Sijing Meng
Institutions
- Cornell University (US)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-02-18
- DOI
- https://doi.org/10.1021/acs.joc.5c03243
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00