Novel porous organocatalysts for cycloaddition of CO2 and epoxides
Joel M Kolle1, Abdelhamid Sayari1
1Centre for Catalysis Research and Innovation (CCRI), Department of Chemistry, University of Ottawa Ottawa Ontario Canada K1N 6N5 Abdel.Sayari@uottawa.ca.
Abstract:
Three classes of organosilicas (DMO, OMOs and PMOs) containing immobilized multi-hydroxyl bis-(quaternary ammonium) iodide salts were prepared and tested in the cycloaddition of CO2 and epoxides. Owing to its higher surface area, pore volume and optimum nucleophilicity of the iodide ion, OMO-2 with two hydroxyl groups was found to be the most active catalyst. For substrates that are easy to activate such as propylene oxide, 1,2-epoxybutane and epichlorohydrin, excellent yields and selectivities were obtained under mild reaction conditions (0.5 MPa CO2, 50 °C and 10-15 h). Moreover, OMO-2 showed very good catalytic properties (yield ≥ 93% and selectivity ≥ 98%), and excellent chemical and textural stability in the synthesis of 1,2-butylene carbonate over 5 cycles.
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