Metal/Oxide Interface Enabling Selective Electrocatalytic Reduction of Oxime to Amine in Neutral Electrolyte
Electrochemical reduction of oximes promises a sustainable route for amine synthesis but is currently limited by the lack of mild electrolyte and low-cost catalyst systems. Here, we for the first time report selective electroreduction of a series of oximes to their corresponding amines in a pH-neutral aqueous electrolyte enabled by a Pb-PbO catalyst. Taking acetoxime as a model reactant, we find that the coexistence of Pb and PbO phases in the catalyst structure is essential for the high Faradaic efficiency and near-unity product selectivity for isopropylamine. Mechanistic studies reveal that the reduction starts with a rate-determining proton-coupled electron transfer step and proceeds through 2-propanimine as an intermediate. The same electrocatalyst also demonstrates high selectivity for other structurally diverse oxime reactants. These findings highlight the critical role of the metal/oxide interface in promoting selective and generalizable electrosynthesis of amines from oximes under mild conditions.
Authors
- Conor L. Rooney (ORCID: https://orcid.org/0000-0001-7058-568X)
- Kunpeng Yu (ORCID: https://orcid.org/0009-0004-0789-6601)
- Nia J. Harmon (ORCID: https://orcid.org/0000-0002-4117-4088)
- Yuanzuo Gao
- Hailiang Wang (ORCID: https://orcid.org/0000-0003-4409-2034)
- Bo Shang (ORCID: https://orcid.org/0000-0002-2294-6062)
- Jing Li (ORCID: https://orcid.org/0000-0001-7538-246X)
- Qi Sun (ORCID: https://orcid.org/0000-0002-8764-5877)
Institutions
- Yale University (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-11-11
- DOI
- https://doi.org/10.1021/jacs.5c13749
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94