Schiff Base Structured Acid–Base Cooperative Dual Sites in an Ionic Solid Catalyst Lead to Efficient Heterogeneous Knoevenagel Condensations

An acid–base bifunctional ionic solid catalyst [PySaIm]₃PW was synthesized by the anion exchange of the ionic‐liquid (IL) precursor 1‐(2‐salicylaldimine)pyridinium bromide ([PySaIm]Br) with the Keggin‐structured sodium phosphotungstate (Na₃PW). The catalyst was characterized by FTIR, UV/Vis, XRD, SEM, Brunauer–Emmett–Teller (BET) theory, thermogravimetric analysis, ¹H NMR spectroscopy, ESI‐MS, elemental analysis, and melting points. Together with various counterparts, [PySaIm]₃PW was evaluated in Knoevenagel condensation under solvent and solvent‐free conditions. The Schiff base structure attached to the IL cation of [PySaIm]₃PW involves acidic salicyl hydroxyl and basic imine, and provides a controlled nearby position for the acid–base dual sites. The high melting and insoluble properties of [PySaIm]₃PW are relative to the large volume and high valence of PW anions, as well as the intermolecular hydrogen‐bonding networks among inorganic anions and IL cations. The ionic solid catalyst [PySaIm]₃PW leads to heterogeneous Knoevenagel condensations. In solvent‐free condensation of benzaldehyde with ethyl cyanoacetate, it exhibits a conversion of 95.8 % and a selectivity of 100 %; the conversion is even much higher than that (78.2 %) with ethanol as a solvent. The solid catalyst has a convenient recoverability with only a slight decrease in conversion following subsequent recyclings. Furthermore, the new catalyst is highly applicable to many substrates of aromatic aldehydes with activated methylene compounds. On the basis of the characterization and reaction results, a unique acid–base cooperative mechanism within a Schiff base structure is proposed and discussed, which thoroughly explains not only the highly efficient catalytic performance of [PySaIm]₃PW, but also the lower activities of various control catalysts.