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Updated: Jan 12, 2026

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Cerium(III) Azolate Promoted CO2 Insertion
Jonas Riedmaier1, Cäcilia Maichle-Mössmer1, Reiner Anwander1
1Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, Tübingen 72076, Germany.
New cerium azolate complexes were synthesized and tested for carbon dioxide (CO2) reactivity. Some complexes readily insert CO2, forming novel structures, while others show limited reactivity, impacting potential catalytic applications.
Area of Science:
- Organometallic Chemistry
- Coordination Chemistry
- Materials Science
Background:
- Cerium complexes offer unique electronic properties for chemical transformations.
- Azolates are versatile ligands in coordination chemistry.
- CO2 utilization remains a critical challenge in sustainable chemistry.
Purpose of the Study:
- Synthesize novel sandwich cerium azolate complexes.
- Investigate the carboxophilicity (CO2 reactivity) of these complexes.
- Evaluate their potential in CO2 cycloaddition catalysis.
Main Methods:
- Synthesis via salt-metathesis and protonolysis protocols.
- Characterization of cerium azolate complexes.
- Probing CO2 insertion reactions and catalytic activity.
Main Results:
- Exhaustive CO2 insertion observed in pyrazolate complexes, forming dimeric structures.
- Steric and electronic factors influence CO2 insertion extent.
- Triazolate and tetrazolate complexes show varied CO2 reactivity.
- Catalytic activity in CO2 and propylene oxide cycloaddition was examined.
Conclusions:
- Ligand design significantly impacts the CO2 reactivity of cerium azolates.
- These complexes demonstrate potential as platforms for CO2 functionalization.
- Further studies are warranted to optimize catalytic performance.
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