Tungstate ion (WO42-) confined in hydrophilic/hydrophobic nanomaterials functionalized brönsted acidic ionic liquid as highly active catalyst in the selective aerobic oxidation of alcohols in water
elemental analysis confirmed that both imidazolium cation and tungstate anion of zwitterion are successfully incorporated inside the organosilica framework. The catalytic activity of resulting hybrid PMO-IL- WO42- material was studied in the selective aerobic oxidation of primary and secondary alcoholsusing an atmospheric pressure of air in pure water. Due to the ionic liquid-based charged surface containing
Phosphotungstic acid (H3PW12O40) has been successfully loaded onto sulfonate-functionalized ionic liquid-modified mesoporous silica SBA-15 by complete anion exchange. The obtained catalysts were highly effective for alkylation of o-xylene with styrene in terms of yield and stability.
Imidazolium-silica heterogeneous catalyst (SG-[(CH2)(3)SO3H-HIM]HSO4) was prepared by immobilization of acidic ionic liquid 1-(propyl-3-sulfonate) imidazolium hydrosulfate ([(CH2)(3)SO3H-HIM]HSO4) on silica-gel using tetraethoxysilane (TEOS) as silica source in this study. The properties of the samples were characterized by FT-IR, SEM and TG/DSC. The results suggested that [(CH2)(3)SO3H-HIM]HSO4 had been successfully immobilized on the surface of silica-gel and the immobilized ionic liquid catalyst SG-[(CH2)(3)SO3H-HIM]HSO4 had good thermal stability. The original smooth surface of silica-gel was covered with [(CH2)(3)SO3H-HIM]HSO4 and a rough surface of SG-[(CH2)(3)SO3H-HIM]HSO4 was formed, but the size of particles had no obvious change. Moreover, SG-[(CH2)(3)SO3H-HIM]HSO4 exhibited high catalytic activity for a series of acetalization and could be recovered easily. After reused for 10 times in the synthesis of benzaldehyde ethanediol acetal, the catalyst could still give satisfactory catalytic activity. (C) 2011 Elsevier B.V. All rights reserved.