4.7 Article

Electrostatic immobilization of phosphomolybdic acid on imidazolium-based mesoporous organosilicas for catalytic olefin epoxidation

Journal

CHINESE JOURNAL OF CATALYSIS
Volume 35, Issue 4, Pages 532-539

Publisher

SCIENCE PRESS
DOI: 10.1016/S1872-2067(14)60025-5

Keywords

Polyoxometalate; Mesoporous organosilica; Imidazolium cation; Electrostatic interaction; EpoxidatIon; Heterogeneous catalysis

Funding

  1. China Scholarship Council and the National Natural Science Foundation of China [21173100]

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Polyoxometalate-based heterogeneous materials were prepared by the immobilization of 12-phosphomolybdic acid (PMA) on periodic mesoporous organosilicas containing embedded imidazolium cations (PMO-ILs). The resulting hybrid materials (PMA@PMO-ILs) were characterized by N-2 adsorption-desorption, powder X-ray diffraction, atomic adsorption spectroscopy, thermogravimetric and differential thermal analyses, Fourier transform infrared spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy, and solid-state cross-polarization magic angle spinning nuclear magnetic resonance. PMA was electrostatically immobilized on the surface and in the channels of PMO-ILs. The PMO-IL support and PMA structures were retained during the preparation processes. The catalytic properties of the PMA@PMO-ILs were evaluated for the liquid-phase epoxidation of cyclooctene. PMA@PMO-ILs were catalytically active, with nearly 100% selectivity to cyclooctene epoxide using tert-butyl hydroperoxide as the oxidant. The catalysts could be reused four times without obvious loss of activity or selectivity under identical reaction conditions. Imidazolium cations in the PMO-IL framework improved the stability and recyclability of the PMA immobilized catalysts. (C) 2014, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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