Two in one: aluminum porphyrin-based porous organic polymers containing symmetrical quaternary phosphonium salts for catalytic conversion of CO 2 into cyclic carbonates.

Based on the double activation models of epoxides, the design and synthesis of ionic porous organic polymers (iPOPs) is considered to be very attractive and promising but has remained a great challenge in recent decades owing to electrostatic interactions between charged groups. In this contribution, we developed a two-in-one strategy to fabricate metalloporphyrin-based iPOPs with unique nanostructures (named AlPor-QP@POP), which are composed of aluminum porphyrin units and three-dimensional quaternary phosphonium salts that work synergistically in the cycloaddition of CO 2 with epoxides under mild conditions. The high symmetry of two monomers allows them to possess similar reactivity ratios and thus endows AlPor-QP@POP with densely located active sites, a large surface area and good CO 2 capture capacity. More importantly, bifunctional AlPor-QP@POP has enormous potential to produce cyclic carbonates with simulated flue gas under ambient conditions. Moreover, AlPor-QP@POP can be readily recycled and efficiently reused more than ten times without an obvious decrease in catalytic activity. Finally, kinetic investigations and a comparative study have been conducted to understand the possible mechanism of CO 2 catalytic cycloaddition.