Abstract
The high active catalyst, polypyrazoles, is designed and synthesized for the cycloaddition of CO 2 with epoxides to give a high yield of cyclic carbonates under mild conditions. Notably, the easy transition between the solid phase and liquid phase of polypyrazole can be realized by temperature adjustment, providing a novel guideline for the design of catalyst. The cycloaddition between CO 2 and epoxides to produce cyclic carbonate is an attractive and efficiency pathway for the utilization of CO 2 as C1 source. The development of catalyst to mediate cycloaddition between CO 2 and epoxides at low temperature and pressure is still a challenge. Herein, a series of polypyrazoles with glass transition temperature ( T g ) in the range of 42.3–52.5 °C were synthesized and served as catalyst to mediate the cycloaddition of CO 2 and epoxides by the assistant of tetrabutylammonium bromide. The catalytic behaviors of polypyrazole on the model cycloaddition of CO 2 to epichlorohydrin, including the reaction parameters optimization and versatility were investigated in detail, and excellent yield (99.9%) and selectivity (99%) were obtained under the optimized reaction conditions of 70 °C and 1.0 MPa for 6.0 h. Noteworthily, the polypyrazole acts as homogeneous catalyst during reaction (higher than T g ). And under room temperature, polypyrazoles can be easily separated and recovered, which is a promising feature of a heterogeneous catalyst. Furthermore, the reaction mechanism was proposed. The DFT calculation suggested that the formation of hydrogen bond between pyrazole and epoxide greatly reduced the energy barrier, which play an important role in promoting CO 2 cycloaddition.
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