Solution infiltration of palladium into MOF-5: synthesis, physisorption and catalytic properties

被引:420
作者
Sabo, Michal
Henschel, Antje
Froede, Heidrun
Klemm, Elias
Kaskel, Stefan [1 ]
机构
[1] Tech Univ Dresden, Dept Inorgan Chem, D-01069 Dresden, Germany
[2] Tech Univ Chemnitz, Dept Chem Technol, D-09111 Chemnitz, Germany
关键词
D O I
10.1039/b706432b
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
Palladium was infiltrated into the highly porous metal-organic framework MOF-5 {[Zn4O(bdc)(3)], bdc = benzene-1,4-dicarboxylate} using [Pd( acac)(2)] ( acac = acetylacetonate) as the precursor in chloroform solution via 'incipient wetness' impregnation. The specific surface area decreases from 2885 m 2 g 21 to 958 m 2 g(-1) after infiltration. After reduction in hydrogen or under vacuum, the hydrogen adsorption capacity is increased from 1.15 wt% to 1.86 wt% at 1 atm and 77 K. The palladium loaded MOF-5 has a high catalytic activity in styrene hydrogenation comparable to that of palladium on activated carbon, but cis-cyclooctene hydrogenation is considerably slower. Even at room temperature, the catalyst is not stable in air due to the low hydrothermal stability of the MOF-5 support.
引用
收藏
页码:3827 / 3832
页数:6
相关论文
共 24 条
[1]   Probing the Lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC = benzene-1,3,5-tricarboxylate) [J].
Alaerts, Luc ;
Seguin, Etienne ;
Poelman, Hilde ;
Thibault-Starzyk, Frederic ;
Jacobs, Pierre A. ;
De Vos, Dirk E. .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (28) :7353-7363
[2]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[3]   A route to high surface area, porosity and inclusion of large molecules in crystals [J].
Chae, HK ;
Siberio-Pérez, DY ;
Kim, J ;
Go, Y ;
Eddaoudi, M ;
Matzger, AJ ;
O'Keeffe, M ;
Yaghi, OM .
NATURE, 2004, 427 (6974) :523-527
[4]   A chemically functionalizable nanoporous material [Cu3(TMA)2(H2O)3]n [J].
Chui, SSY ;
Lo, SMF ;
Charmant, JPH ;
Orpen, AG ;
Williams, ID .
SCIENCE, 1999, 283 (5405) :1148-1150
[5]   Rigid and flexible: A highly porous metal-organic framework with unusual guest-dependent dynamic behavior [J].
Dybtsev, DN ;
Chun, H ;
Kim, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (38) :5033-5036
[6]   Modular chemistry: Secondary building units as a basis for the design of highly porous and robust metal-organic carboxylate frameworks [J].
Eddaoudi, M ;
Moler, DB ;
Li, HL ;
Chen, BL ;
Reineke, TM ;
O'Keeffe, M ;
Yaghi, OM .
ACCOUNTS OF CHEMICAL RESEARCH, 2001, 34 (04) :319-330
[7]  
Férey G, 2005, SCIENCE, V310, P1119
[8]   Metal@MOF:: Loading of highly porous coordination polymers host lattices by metal organic chemical vapor deposition [J].
Hermes, S ;
Schröter, MK ;
Schmid, R ;
Khodeir, L ;
Muhler, M ;
Tissler, A ;
Fischer, RW ;
Fischer, RA .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (38) :6237-6241
[9]   Loading of porous metal-organic open frameworks with organometallic CVD precursors:: inclusion compounds of the type [LnM]a@MOF-5 [J].
Hermes, Stephan ;
Schroeder, Felicitas ;
Amirjalayer, Saeed ;
Schmid, Rochus ;
Fischer, Roland A. .
JOURNAL OF MATERIALS CHEMISTRY, 2006, 16 (25) :2464-2472
[10]  
Kaskel S, 2002, HDB POROUS SOLIDS, P1190, DOI DOI 10.1002/9783527618286.CH19