Scalable and Recyclable All-Organic Colloidal Cascade Catalysts

We report on the synthesis of core-shell microparticles (CSMs) with an acid catalyst in the core and a base catalyst in the shell by surfactant-free emulsion polymerization (SFEP). The organocatalytic monomers were separately copolymerized in three synthetic steps allowing the spatial separation of incompatible acid and base catalysts within the CSMs. Importantly, a protected and thermo-decomposable sulfonate monomer was used as acid source to circumvent the neutralization of the base catalyst during shell formation, which was key to obtain stable, catalytically active CSMs. The catalysts showed excellent performance in an established one-pot model cascade reaction in various solvents (including water), which involved an acid-catalyzed deacetalization followed by a base-catalyzed Knoevenagel condensation. The CSMs are easily recycled, modified, and their synthesis is scalable, making them promising candidates for organocatalytic applications.

Automated summary

Core-shell microparticles (CSMs) were successfully synthesized with an acid catalyst in the core and a base catalyst in the shell by surfactant-free emulsion polymerization (SFEP). These CSMs exhibited excellent catalytic performance in a model cascade reaction, making them promising candidates for organocatalytic applications in various solvents.