Robust multivariate metal-porphyrin frameworks for efficient ambient fixation of CO2 to cyclic carbonates.

A family of multivariate metal-organic frameworks (MOFs) with three-kinds of orderly distributed metals were designed and successfully synthesized by combining metalloporphyrin sheets and pentafluoride (NbOF5)2- pillars. Benefiting from the cooperative nature of open-metal-sites (OMSs) within porphyrins, specific pore-sizes, coupled with fluorine-rich electrostatic environments, the fabricated materials demonstrated high affinity toward CO2, and good catalytic performance, structural robustness, and good recyclability for the conversion of epoxides and CO2 to cyclic carbonates at room temperature and 1 atm pressure.

Dual-cubic-cage based lanthanide sulfate-carboxylpyrazolate frameworks with high hydrolytic stability and remarkable proton conduction.

We report herein a series of lanthanide sulfate-carboxylpyrazolate frameworks based on double cuboid cavities that are highly hot-water stable, and have room-temperature proton conductivity of over 10-3 S cm-1 at 97% relative humidity without any appreciable loss of performance for at least three recycling times, ranking among the best lanthanide-based coordination frameworks.