Ionic Porous Aromatic Frameworks Embedding Polyoxometalates for Heterogeneous Catalysis

Abstract

AbstractPorous aromatic frameworks (PAFs) are highly promising functional porous solids known for their feasible amenability and extraordinary stability. When the framework was modified by ionic functional groups, these ionic PAFs (iPAFs) exhibited charged channels for adsorption, separation, and catalysis. However, the surface areas of ionic porous frameworks are usually lower than that of neutral frameworks, and their synthesis is limited by specific strategies and complex modification processes. To address these challenges, an intuitive route to construct ionic porous framework with high specific surface area was proposed. Herein, a multivariate ionic porous aromatic framework (MTV‐iPAFs, named PAF‐270) was synthesized using readily available building units with ionic functional groups through a multivariable synthesis strategy. PAF‐270 exhibited hierarchical structure with the highest specific surface area among reported imidazolium‐functionalized PAFs. Utilizing its physical and chemical properties, the availability for polyoxometalate loading and heterogeneous catalysis of PAF‐270 were explored. PAF‐270 exhibited a high adsorption capacity up to 50 % for both H3O40PW12 (HPW) and (NH4)5H6PV8Mo4O40 (V8). HPW@PAF‐270 and V8@PAF‐270 exhibited excellent catalytic abilities for oleic acid esterification and extractive oxidative desulfurization, respectively. Due to the stability of PAFs, these materials also showed remarkable resistance to temperature and pH changes. Overall, these results underscore the potential application of MTV‐iPAFs as versatile functional porous materials.