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.

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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
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article

Scalable Main Group Mechanocatalytic CO 2 Valorisation to Cyclocarbonate Species

Javier F. Reynes, Felipe Garcı́a, Marta E. G. Mosquera, Christopher J. Whiteoak et al.
5 citations
Angewandte Chemie International Edition
Carbon dioxide utilization in catalysis
3.52
article

Scalable Main Group Mechanocatalytic CO 2 Valorisation to Cyclocarbonate Species

Javier F. Reynes, Felipe Garcı́a, Marta E. G. Mosquera, Christopher J. Whiteoak, Lucía Álvarez‐Miguel, Michael Felderhoff, F. Winkelmav
article en
5 citations

Abstract

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.

Angewandte Chemie International EditionVol. 64(27)
Universidad de Oviedo (ES), Universidad de Alcalá (ES), Max-Planck-Institut für Kohlenforschung (DE), Monash University (AU)
Life in Land
Openalex Percentile: Top 8%
Carbon dioxide utilization in catalysis
3.52
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