Metal organic frameworks (MOFs) as catalysts:: A combination of Cu2+ and Co2+ MOFs as an efficient catalyst for tetralin oxidation

被引:256
作者
Llabres i Xamena, F. X. [1 ]
Casanova, O. [1 ]
Galiasso Tailleur, R. [1 ]
Garcia, H. [1 ]
Corma, A. [1 ]
机构
[1] Univ Politecn Valencia, CSIC, Inst Tecnol Quim, Valencia 46022, Spain
关键词
metal-organic framework; coordination polymer; tetralin aerobic oxidation;
D O I
10.1016/j.jcat.2008.02.011
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
Two metal-organic frameworks, [Cu(2-pymo)(2)] and [Co(PhIM)(2)] (2-pymo = 2-hydroxypyrimidinolate; PhIM = phenylimidazolate), containing respectively Cu2+ and Co2+ ions and anionic diazaheterocychc ligands (pyrimidinolate and phenylimidazolate) as organic linkers, have been successfully used for the aerobic oxidation of tetralin, yielding a-tetralone (T=O) as the main product. Both materials are stable and recyclable under the reaction conditions. Kinetic studies revealed significant differences between the two MOFs, as a consequence of the different catalytic behavior of their central metal ions. [Cu(2-pymo)(2)] is highly active for the activation of tetralin to produce tetralinhydroperoxide (T-OOH), and less efficient in reacting the peroxide. Meanwhile, the use of the cobalt catalyst involves a long induction period for the reaction. However, once T-OOH is formed, Co2+ rapidly and efficiently transforms this into T=O, with high tetralone-to-tetralol ratio (T=O/T-OH of ca. 7). The combination of both materials has revealed as a convenient strategy for preparing a highly efficient, selective and reusable catalyst for the liquid phase aerobic oxidation of tetralin. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:220 / 227
页数:8
相关论文
共 38 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]   AUTOXIDATION OF TETRALIN CATALYZED BY COBALT PYRIDINE COMPLEXES IN POLYMER LATEXES [J].
CHANDRAN, RS ;
SRINIVASAN, S ;
FORD, WT .
LANGMUIR, 1989, 5 (04) :1061-1071
[3]   AUTOXIDATION OF TETRALIN IN WATER CATALYZED BY COBALT(II) PYRIDINE COMPLEXES BOUND TO POLYMER COLLOIDS [J].
CHANDRAN, RS ;
FORD, WT .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (02) :104-105
[4]   A metal-organic framework material that functions as an enantioselective catalyst for olefin epoxidation [J].
Cho, So-Hye ;
Ma, Baoqing ;
Nguyen, SonBinh T. ;
Hupp, Joseph T. ;
Albrecht-Schmitt, Thomas E. .
CHEMICAL COMMUNICATIONS, 2006, (24) :2563-2565
[5]   Attempts to fill the gap between enzymatic, homogeneous, and heterogeneous catalysis [J].
Corma, A .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2004, 46 (3-4) :369-417
[6]   State of the art and future challenges of zeolites as catalysts [J].
Corma, A .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :298-312
[7]  
CORMA A, 2006, Patent No. 1632468
[8]   Are heterogeneous catalysts precursors to homogeneous catalysts? [J].
Davies, IW ;
Matty, L ;
Hughes, DL ;
Reider, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (41) :10139-10140
[9]   Synthesis, characterization, and some properties of 4-vinylpyridine-Cr(CO)5 containing polymers [J].
Fares, MM ;
El-Khateeb, M ;
Asali, KJ .
JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS, 2003, 13 (03) :143-155
[10]   Crystallized frameworks with giant pores:: Are there limits to the possible? [J].
Férey, G ;
Mellot-Draznieks, C ;
Serre, C ;
Millange, F .
ACCOUNTS OF CHEMICAL RESEARCH, 2005, 38 (04) :217-225