Ni2+-containing ionic liquid immobilized on silica: Effective catalyst for styrene oxidation with H2O2 at solvent-free condition

In this work we synthesized Ni2+-containing ionic liquid (IL) 1-methyl-3-[(triethoxysilyl)propyl]imidazolium chloride (TMICl) immobilized on silica to catalyze styrene oxidation with H2O2 for producing benzaldehyde. The catalyst was characterized by Fourier transform infrared (FT-IR) spectroscopy, UV–vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and nitrogen sorption techniques. The effects of reaction time, reaction temperature, and molar ratio of styrene and H2O2 on the conversion and selectivity were studied at solvent-free condition and in acetonitrile. It was demonstrated that the catalyst was very effective for the reaction. The unique advantage of the catalyst was that the reaction could be carried out at solvent-free condition. This advantage resulted mainly from the fact that both of the reactants, styrene and H2O2, are miscible with the IL, and the Ni2+ was coordinated by the immobilized IL that allowed both reactants to access to active sites of the catalyst effectively.

Ni2+-containing ionic liquid N-3-(3-triethoxysilypropyl)-1-methyl imidazolium chloride immobilized on silica can catalyze styrene oxidation with H2O2 to produce benzaldehyde effectively under solvent-free condition. The unique advantage of the catalyst was that the reaction could be carried out at solvent-free condition. This advantage resulted mainly from the fact that both of the reactants, styrene and H2O2, are miscible with the IL, and the Ni2+ was coordinated by the immobilized IL that allowed both reactants to access to active sites of the catalyst effectively.Figure optionsDownload as PowerPoint slide