Scalable Main Group Mechanocatalytic CO <sub>2</sub> Valorisation to Cyclocarbonate Species
Over the past two decades, main group elements have gained attention as promising substitutes for precious metals in catalytic processes. Additionally, mechanochemistry is emerging as a field with the potential to promote catalytic reactions under mild conditions. Herein, we report a scalable, main-group mechanocatalytic synthesis of cyclic carbonates from both solid and liquid epoxides, using CO₂ as a renewable feedstock under mild conditions with a gallium aminotrisphenolate catalyst. Unlike solution-based methods that generally require high temperatures and/or high CO₂ pressures, this mechanocatalytic process operates at just 1 bar and room temperature. The developed mechanochemical method affords the targeted compounds in high yields while also enabling efficient transformation of multi-terminal epoxides and avoiding the conversion losses typically observed in solution. Furthermore, this scalable method outperforms solution-based approaches across all green metrics, setting a new benchmark for environmentally friendly synthesis.
Authors
- Javier F. Reynes (ORCID: https://orcid.org/0000-0002-1400-3531)
- Felipe Garcı́a (ORCID: https://orcid.org/0000-0002-9605-3611)
- Marta E. G. Mosquera (ORCID: https://orcid.org/0000-0003-2248-3050)
- Christopher J. Whiteoak (ORCID: https://orcid.org/0000-0003-1501-5582)
- Lucía Álvarez‐Miguel (ORCID: https://orcid.org/0000-0002-6748-1158)
- Michael Felderhoff (ORCID: https://orcid.org/0000-0001-9526-3943)
- F. Winkelmav
Institutions
- Universidad de Oviedo (ES)
- Universidad de Alcalá (ES)
- Max-Planck-Institut für Kohlenforschung (DE)
- Monash University (AU)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2025-04-24
- DOI
- https://doi.org/10.1002/anie.202502584
- Citations
- 5
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 3.52