Building MOF bottles around phosphotungstic acid ships: One-pot synthesis of bi-functional polyoxometalate-MIL-101 catalysts

磷钨酸 多金属氧酸盐 化学 催化作用 Knoevenagel冷凝 醋酸 二苯乙炔 苯甲醛 甲醇 甲苯 多相催化 浸出(土壤学) 溶剂 核化学 无机化学 有机化学 土壤水分 土壤科学 环境科学
作者
Jana Juan‐Alcañiz,Enrique V. Ramos‐Fernández,Ugo Lafont,Jorge Gascón,Freek Kapteijn
出处
期刊:Journal of Catalysis [Elsevier BV]
卷期号:269 (1): 229-241 被引量:324
标识
DOI:10.1016/j.jcat.2009.11.011
摘要

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.
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