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A novel magnetic nanoparticle supported dual acidic ionic liquid catalyst was synthesized by anchoring 3-sulfobutyl-1-(3-propyltriethoxysilane) imidazolium hydrogen sulfate onto the surface of silica-coated Fe 3 O 4 nanoparticles. Due to the combination of nano-support features and flexible imidazolium linkers, it acted as a "quasi-homogeneous" catalyst to effectively catalyze the one-pot synthesis of benzoxanthenes by a three-component condensation of dimedone with aldehyde and 2-naphthol under solvent-free conditions. More importantly, the catalyst could be easily recovered by an external magnet and reused six times without significant loss of catalytic activity.

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A novel magnetic nanoparticle-supported nano-palladium catalyst was successfully prepared via a ''click'' route. The as-prepared catalyst was well characterized and evaluated in Suzuki-Miyaura coupling in terms of activity and recyclability in aqueous ethanol. It was found to be highly efficient for the reactions of various aryl bromides with arylboronic acids under phosphine-free and low Pd loading (0.2 mol%) conditions. Moreover, the catalyst could be easily separated from the reaction system by an external magnet and reused several times without a remarkable loss of its activity.