Issue 22, 2024

Bioinspired copper-catalysed nitrous oxide reduction with simultaneous N–H or O–H bond oxidation

Abstract

Herein, we report on a bioinspired reduction of nitrous oxide in the presence of hydrogen-donating molecules, which are simultaneously oxidised. The copper-/TEMPO-based molecular catalyst has been previously reported to oxidise, for example, alcohols to aldehydes, diols to lactones, amines to imines, and, more recently, for the N-formylation of amines with methanol using (aerial) oxygen as a terminal oxidant. In this report, we demonstrate that it is possible to decompose nitrous oxide, a natural greenhouse gas and industrial waste gas, at low temperatures. This process simultaneously enables the oxidation of amines to imines and the formation of aminoacetal/aminal through the addition and oxidation of methanol. In this context, the Cu/TEMPO catalyst mimics nitrous oxide reductase (N2OR) and alcohol oxidase (AO) simultaneously. The catalyst is formed in situ from inexpensive and commercially available precursors. Selectivities and yields can be controlled by varying the composition of the substrate mixture and oxidant. This approach is attractive for the synthetic valorisation of organic molecules and utilisation of nitrous oxide, which remains a critical greenhouse gas and a byproduct of large-scale industrial processes, such as fertilizer production. These reactions, facilitated by a robust and affordable catalyst, are easy to carry out, making them highly practical for industrial applications.

Graphical abstract: Bioinspired copper-catalysed nitrous oxide reduction with simultaneous N–H or O–H bond oxidation

Supplementary files

Article information

Article type
Paper
Submitted
19 Jun 2024
Accepted
05 Aug 2024
First published
10 Sep 2024

Catal. Sci. Technol., 2024,14, 6503-6512

Bioinspired copper-catalysed nitrous oxide reduction with simultaneous N–H or O–H bond oxidation

B. A. Lobo Sacchelli, S. M. P. Onguene, R. S. M. Almeida, A. M. M. Antunes, D. S. Nesterov, L. H. Andrade, E. C. B. A. Alegria and M. H. G. Prechtl, Catal. Sci. Technol., 2024, 14, 6503 DOI: 10.1039/D4CY00760C

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