EventsThe 4th International Electronic Conference on Catalysis Sciences
Published
This submission belongs to the session S7. Catalysis in Organic and Polymer Chemistry of the event The 4th International Electronic Conference on Catalysis Sciences
Published date
17 Sep, 2026
Academic Editor
author-avatarRaffaella Mancuso
Citation
Sylwia Kostera, Alberto Gobbo, Massimo Guelfi, Stefano Zacchini, Gabriele Manca, Fabio Marchetti, Luca Gonsalvi, RU-TRIS(PYRAZOLYL)METHANE COMPLEXES AS ACTIVE CATALYSTS FOR THE HOMOGENEOUS HYDROGENATION OF CO₂ TO FORMATE, in Proceedings of The 4th International Electronic Conference on Catalysis Sciences, 22 September–24 September 2026, MDPI: Basel, Switzerland
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RU-TRIS(PYRAZOLYL)METHANE COMPLEXES AS ACTIVE CATALYSTS FOR THE HOMOGENEOUS HYDROGENATION OF CO₂ TO FORMATE

Alberto Gobbo 2
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1. Institute of Chemistry of Organometallic Compounds (ICCOM), National Research Council of Italy (CNR), Via Madonna del Piano 10, 50019 Sesto Fiorentino (Florence), Italy
2. Department of Chemistry and Industrial Chemistry, University of Pisa, Via Moruzzi 13, 56124 Pisa, Italy
3. Department of Industrial Chemistry "Toso Montanari", University of Bologna, Via Gobetti 85, Bologna, Italy
4. Institute of Chemistry of Organometallic Compounds (ICCOM), Bari Secondary Site, National Research Council of Italy (CNR), Via Orabona 4, 70126 Bari, Italy
Abstract

Over the past ten years, there has been a renewed focus on using CO₂ as a readily available, renewable, and economical starting material for the synthesis of C1 chemicals. The environmentally sustainable production of formic acid through CO₂ hydrogenation is particularly noteworthy, given its diverse applications in fields such as agriculture (for silage), food preservation, and wood pulping. In this context, a series of cationic Ru(κ³-tpm) piano-stool complexes [where tpm = tris(pyrazolyl)methane], with various auxiliary ligands, were evaluated in our laboratories for their ability to catalyze the hydrogenation of CO₂ to formate in homogeneous phase. These reactions were performed both with and without a Lewis acid co-catalyst, achieving high product yields (>99%) and turnover numbers (TONs) exceeding 54,000 under mild conditions. Finally, proof-of-concept experiments demonstrated that the catalyst solution can be efficiently recycled for consecutive runs without significant loss of activity. The presented results showcase the potential of tris(pyrazolyl)methane complexes in catalytic reactions of high current interest that have previously been neglected, and they pave the way for further studies in other CO₂ reduction processes. Key findings, along with mechanistic insights derived from NMR analysis and DFT calculations, will be discussed. This research was supported by Project POR H2 AdP funded by the European Union – NextGeneration EU through the Italian Ministry of Environment and Energy Security, PNRR - Mission 2, Component 2, Investment 3.5 “Ricerca e sviluppo sull’idrogeno”.

Keywords
CO2 hydrogenation
Ruthenium complexes
Tris(pyrazolyl)methane
Homogeneous catalysis
Mechanistic studies
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