Water Serving as Cocatalyst for the Highly Efficient Homogeneously Catalyzed Conversion of N <sub>2</sub> O/H <sub>2</sub> Mixtures with Optimized Rhodium NHC Complexes

S Sven Thomas Nappen (Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland) J Juan José Gamboa‐Carballo (Institut Des Sciences Analytiques Et De Physico‐Chimie pour L'environnement Et Les Matériaux (UMR 5254) CNRS/Université De Pau et Des Pays de L'adour Hélioparc France) E Esther Tschanen (Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland) F Federica Ricatto (Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland) M Michael Dieter Wörle (Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland) A Arne Thomas (Functional Materials, Department of Chemistry, Technische Universität Berlin, Hardenbergstraße 40, Berlin 10623, Germany) M Monica Trincado (Department of Chemistry University of Zürich Winterthurerstrasse 190 Zurich CH‐8057 Switzerland) H Hansjörg Grützmacher (Laboratory of Inorganic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir Prelog Weg 1, Zürich CH-8093, Switzerland)

Abstract

Abstract Nitrous oxide (N 2 O) is a valuable oxygen/nitrogen transfer reagent but reactions with N 2 O are challenging due to its inertness. Consequently, it accumulates in the atmosphere, and because it is both an ozone‐depleting reagent and potent green‐house gas, effective mitigation methods become important. This study presents rhodium(I) amido bis(olefin) N ‐heterocyclic carbene complexes [Rh(trop 2 N)(NHC)] as robust homogeneous catalysts for the direct hydrogenation of N 2 O. Kinetic experiments and DFT calculations show that increasing π ‐acidity of the NHC and the presence of water significantly enhance the catalytic efficiency. The rhodium‐amido bond facilitates cooperative H 2 ‐cleavage and oxygen atom transfer from N 2 O. The catalyst is regenerated with the loss of water from the hydroxide intermediate [Rh(OH)(trop 2 NH)(NHC)], which forms a dimeric complex with a central bridging hydrated hydroxide ligand [H 3 O 2 ] − . Water facilitates dinitrogen (N 2 ) loss from an intermediate containing an oxy‐diazene ligand [H─N═N─O] − . The optimized catalyst achieves a TON &gt; 230 000 and TOF &gt; 1300 h −1 .

Article Details

Volume / Issue Vol. 64, Issue 25
Published June 17, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

S

Sven Thomas Nappen

Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland

J

Juan José Gamboa‐Carballo

Institut Des Sciences Analytiques Et De Physico‐Chimie pour L'environnement Et Les Matériaux (UMR 5254) CNRS/Université De Pau et Des Pays de L'adour Hélioparc France

E

Esther Tschanen

Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland

F

Federica Ricatto

Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland

M

Michael Dieter Wörle

Department of Chemistry and Applied Biosciences ETH Zürich Vladimir‐Prelog‐Weg 1 Zürich CH‐8093 Switzerland

A

Arne Thomas

Functional Materials, Department of Chemistry, Technische Universität Berlin, Hardenbergstraße 40, Berlin 10623, Germany

M

Monica Trincado

Department of Chemistry University of Zürich Winterthurerstrasse 190 Zurich CH‐8057 Switzerland

H

Hansjörg Grützmacher

Laboratory of Inorganic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir Prelog Weg 1, Zürich CH-8093, Switzerland