Advanced Synthesis & Catalysis · 2019 · 22 citations · 52 references
EngineeringOrganic ChemistryNanocatalysisChemistryCatalytic SelectivityChemical EngineeringGoethite NanoflowerFully Converted NitrostyrenesPhotocatalysisHomogeneous CatalysisCatalytic ApplicationCatalysisHydrogenCatalytic ProcessCatalytic SynthesisChemoselective HydrogenationHeterogeneous CatalysisMolecular CatalysisCatalyst PreparationDesirable Selectivity
Abstract Control of chemoselectivity is a special challenge for the reduction of nitroarenes bearing one or more unsaturated groups. Here, we report a flower‐like Rh/α‐FeOOH catalyst for the chemoselective hydrogenation of nitrostyrene to vinylaniline over full conversion, which benefits the new functionalized aminostyrene because the multisubstituted aminostyrenes are usually commercially unavailable. This catalyst does not only show desirable selectivity for the vinylanilines, but also exhibits the inertness to various other reducible groups over wide reaction duration. The catalytic selectivity for the reduction of the nitro group towards vinyl group was investigated by the control experiments and FT‐IR analysis. We have found that the abundant hydroxyl groups in the α‐FeOOH may contribute to the improvement of catalytic activity and selectivity. Furthermore, the catalyst exhibits excellent stability and keeps its catalytic performance even after 6 cycles. magnified image
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Catalytic syntheses of aromatic amines
R.S. Downing, P.J. Kunkeler, H. van Bekkum · Catalysis Today · 1997 · 578 citations
Mercè Boronat, Patricia Concepción, Avelino Corma et al. · Journal of the American Chemical Society · 2007 · 508 citations