Abstract
A new strategy has been developed for the direct encapsulation of polyoxometalates (POMs) into MIL-101(Cr). The addition of phosphotungstic acid (PTA) to the synthesis mixture of MIL-101 yields the direct encapsulation of chromium-containing polyoxometalates (POMs) inside the MOF structure, with a good distribution over the MIL-101 crystals. Vibrational Spectroscopy (DRIFT, Raman, UV-Vis) reveals the partial substitution of tungsten by Cr3+ resulting in the so-called lacunary structures, which are highly active in catalysis. The medium-sized cavities of MIL-101 are occupied by POM units bigger than their pentagonal windows when this one-pot approach is followed, and no leaching is observed. These new catalysts show the highest activities reported to date at 313 K for the Knoevenagel condensation of benzaldehyde with ethyl cyanoacetate when using apolar toluene as solvent as well as when using polar DMF and ethanol, with TOFs exceeding 600 h-1. In addition, they exhibit a remarkable activity in two acid-catalyzed reactions, the esterification of n-butanol with acetic acid in liquid phase slurry operation and the dimethyl ether production from methanol in a fixed bed gas phase operation, in contrast to the poor or absent activity of the catalysts prepared via the impregnation of the polyoxometalate in MIL-101, where the strong interaction between POM and support deteriorates the catalytic performance.
Original language | English (US) |
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Pages (from-to) | 229-241 |
Number of pages | 13 |
Journal | Journal of Catalysis |
Volume | 269 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2010 |
Externally published | Yes |
Keywords
- Bi-functional catalyst
- Encapsulated catalyst
- Esterification
- Etherification
- Knoevenagel condensation
- MIL-101
- Metal organic frameworks
- Phosphotungstic acid
- Polyoxometalates
ASJC Scopus subject areas
- Catalysis
- Physical and Theoretical Chemistry