期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 51, 页码 26639-26646出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202107916
关键词
continuous flow; heterogeneous catalysis; magnetic induction; multifunctional catalyst; selective hydrogenation
资金
- Max Planck Society
- Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy-Exzellenzcluster 2186 The Fuel Science Center [390919832]
- Projekt DEAL
This study presents a magnetically activatable multifunctional catalytic system made by decorating copper chromite with iron carbide nanoparticles, which can efficiently catalyze the reduction of aromatic ketones under magnetic induction. By generating locally confined hot spots under magnetic excitation, the catalyst selectively activates the Cu2Cr2O5 surface while maintaining a low global temperature. The catalytic properties of ICNPs@Cu2Cr2O5 for the hydrogenation of biomass-derived furfuralacetone remain stable for at least 17 hours during continuous operation, marking the first application of a magnetically heated catalyst in a liquid-phase hydrogenation reaction.
Copper chromite is decorated with iron carbide nanoparticles, producing a magnetically activatable multifunctional catalytic system. This system (ICNPs@Cu2Cr2O5) can reduce aromatic ketones to aromatic alcohols when exposed to magnetic induction. Under magnetic excitation, the ICNPs generate locally confined hot spots, selectively activating the Cu2Cr2O5 surface while the global temperature remains low (approximate to 80 degrees C). The catalyst selectively hydrogenates a scope of benzylic and non-benzylic ketones under mild conditions (3 bar H-2, heptane), while ICNPs@Cu2Cr2O5 or Cu2Cr2O5 are inactive when the same global temperature is adjusted by conventional heating. A flow reactor is presented that allows the use of magnetic induction for continuous-flow hydrogenation at elevated pressure. The excellent catalytic properties of ICNPs@Cu2Cr2O5 for the hydrogenation of biomass-derived furfuralacetone are conserved for at least 17 h on stream, demonstrating for the first time the application of a magnetically heated catalyst to a continuously operated hydrogenation reaction in the liquid phase.
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