Gold nanoparticle-decorated reduced graphene oxide as a highly effective catalyst for the selective α,β-dehydrogenation of <i>N</i> -alkyl-4-piperidones
Gold nanoparticles (AuNPs) supported on reduced graphene oxide (AuNPs/rGO) were demonstrated to be a highly reactive catalyst for the selective α,β-oxidative dehydrogenation (ODH) of <i>N</i>-alkyl-4-piperidones, using <i>N</i>-methyl-, <i>N</i>-ethyl- and <i>N</i>-benzyl-4-piperidone. The substrate <i>N</i>-methyl-4-piperidone represents a pharmaceutically relevant system as its reaction product <i>N</i>-methyl-2,3-dihydropyridin-4(1<i>H</i>)-one is highly valuable (>1000 €·g<sup>-1</sup>) in contrast to the inexpensive starting material (0.15 €·g<sup>-1</sup>). Various synthesis methods were employed to prepare AuNPs supported on different carbon materials, including reduced graphene oxide (rGO), activated carbon (AC), and carbon black (CB), to investigate the influence of the carbon support on the catalyst performance. As stabilizing agents for the AuNPs, citrate (Cit) and the polyoxometallate [SiW<sub>9</sub>O<sub>34</sub>]<sup>10-</sup> (SiW<sub>9</sub>) were used. Among the tested catalysts, the rGO-supported ones, Au-Cit/rGO, Au-SiW<sub>9</sub>/rGO, and Au@SiW<sub>9</sub>/rGO exhibited the highest catalytic activity for the selective oxidation reaction despite containing the lowest gold loading. These findings highlight the exceptional performance of rGO as a support for AuNP catalysts and provide valuable insights for designing efficient Au-based systems for the dehydrogenation of β-N-substituted saturated ketones and other fine chemical applications.
Authors
- Marilyn Kaul
- Robert Oestreich
- Aysenur Limon
- Brenda Flore Kenyim
- Mihir Tzalis
- Chancellin Pecheu Nkepdep
- Christoph Janiak
Institutions
- Heinrich Heine University Düsseldorf (DE)
Publication Details
- Journal
- Beilstein Journal of Nanotechnology
- Published
- 2026-01-30
- DOI
- https://doi.org/10.3762/bjnano.17.15
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00