N-Hydroxyphthalimide was immobilized via ester bond on commercially available silica gel (SiOCONHPI) and then coated with various ionic liquids containing dissolved CoCl2 (SiOCONHPI@CoCl2@IL). New catalysts were characterized by means of FT IR spectroscopy, elemental analysis, SEM and TGA analysis and used in ethylbenzene oxidation with oxygen under mild solvent-free conditions (80 °C, 0.1 MPa). High catalytic activity of SiOCONHPI was proved. In comparison to a non-catalytic reaction, a two-fold increase in conversion of ethylbenzene was observed (from 4.7% to 8.6%). Coating of SiOCONHPI with [bmim][OcOSO3], [bmim][Cl] and [bmim][CF3SO3] containing CoCl2 enabled to increase the catalytic activity in relation to systems in which IL and CoCl2 were added directly to reaction mixture. The highest conversion of ethylbenzene was obtained while SiOCONHPI@CoCl2@[bmim][OcOSO3] were used (12.1%). Catalysts recovery and reuse was also studied.
Novel Brönsted Acidic Ionic Liquids Confined in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions