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Schiff Base Structured Acid–Base Cooperative Dual Sites in an Ionic Solid Catalyst Lead to Efficient Heterogeneous Knoevenagel Condensations
Author(s) -
Zhang Mingjue,
Zhao Pingping,
Leng Yan,
Chen Guojian,
Wang Jun,
Huang Jun
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201201338
Subject(s) - knoevenagel condensation , chemistry , catalysis , ionic liquid , schiff base , inorganic chemistry , thermogravimetric analysis , bifunctional , ion exchange , condensation reaction , solvent , organic chemistry , polymer chemistry , ion
An acid–base bifunctional ionic solid catalyst [PySaIm] 3 PW 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 (Na 3 PW). The catalyst was characterized by FTIR, UV/Vis, XRD, SEM, Brunauer–Emmett–Teller (BET) theory, thermogravimetric analysis, 1 H NMR spectroscopy, ESI‐MS, elemental analysis, and melting points. Together with various counterparts, [PySaIm] 3 PW was evaluated in Knoevenagel condensation under solvent and solvent‐free conditions. The Schiff base structure attached to the IL cation of [PySaIm] 3 PW 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] 3 PW 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] 3 PW 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] 3 PW, but also the lower activities of various control catalysts.