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

被引:303
作者
Juan-Alcaniz, Jana [1 ]
Ramos-Fernandez, Enrique V. [1 ]
Lafont, Ugo [1 ]
Gascon, Jorge [1 ]
Kapteijn, Freek [1 ]
机构
[1] Delft Univ Technol, NL-2628 BL Delft, Netherlands
基金
美国国家科学基金会;
关键词
Metal organic frameworks; MIL-101; Polyoxometalates; Phosphotungstic acid; Knoevenagel condensation; Esterification; Etherification; Encapsulated catalyst; Bi-functional catalyst; METAL-ORGANIC-FRAMEWORKS; CHROMIUM TEREPHTHALATE MIL-101; DIMETHYL ETHER; HETEROPOLYACID CATALYSTS; PROTON SPONGE; DEHYDRATION; OXIDATION; METHANOL; SORPTION; CARBON;
D O I
10.1016/j.jcat.2009.11.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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. (c) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:229 / 241
页数:13
相关论文
共 57 条
[1]   Zeolite-like metal-organic frameworks as platforms for applications:: On metalloporphyrin-based catalysts [J].
Alkordi, Mohamed H. ;
Liu, Yunling ;
Larsen, Randy W. ;
Eubank, Jarrod F. ;
Eddaoudi, Mohamed .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (38) :12639-+
[2]   Luminescent metal-organic frameworks [J].
Allendorf, M. D. ;
Bauer, C. A. ;
Bhakta, R. K. ;
Houk, R. J. T. .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (05) :1330-1352
[3]  
[Anonymous], 2001, FINE CHEM HETEROGENE
[4]   Dehydration of glycerol in gas phase using heteropolyacid catalysts as active compounds [J].
Atia, Hanan ;
Armbruster, Udo ;
Martin, Andreas .
JOURNAL OF CATALYSIS, 2008, 258 (01) :71-82
[5]   Solvent effect on the preparation of H3PW12O40 supported on alumina [J].
Caliman, E ;
Dias, JA ;
Dias, SCL ;
Prado, AGS .
CATALYSIS TODAY, 2005, 107-08 :816-825
[6]   Gem-diamines as highly active organocatalysts for carbon-carbon bond formation [J].
Climent, Maria J. ;
Corma, Avelino ;
Dominguez, Irene ;
Iborra, Sara ;
Sabater, Maria J. ;
Sastre, German .
JOURNAL OF CATALYSIS, 2007, 246 (01) :136-146
[7]   Immobilized proton sponge on inorganic carriers [J].
Corma, A ;
Iborra, S ;
Rodríguez, I ;
Sánchez, F .
JOURNAL OF CATALYSIS, 2002, 211 (01) :208-215
[8]   An Amine-Functionalized MIL-53 Metal-Organic Framework with Large Separation Power for CO2 and CH4 [J].
Couck, Sarah ;
Denayer, Joeri F. M. ;
Baron, Gino V. ;
Remy, Tom ;
Gascon, Jorge ;
Kapteijn, Freek .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (18) :6326-+
[9]   A NOVEL TRIPEROXYNIOBIUM-CONTAINING POLYOXOANION, (SIW9(NBO2)3O37)-O-7- - SYNTHESIS, CHARACTERIZATION, CATALYTIC ALLYLIC EPOXIDATIONS WITH H2O2 AND PRELIMINARY KINETIC-STUDIES [J].
DROEGE, MW ;
FINKE, RG .
JOURNAL OF MOLECULAR CATALYSIS, 1991, 69 (03) :323-338
[10]  
FARRUSSENG D, 2009, ANGEW CHEM INT EDITI, V9999