Chromium(III) Terephthalate Metal Organic Framework (MIL-101): HF-Free Synthesis, Structure, Polyoxometalate Composites, and Catalytic Properties

被引:378
作者
Bromberg, Lev
Diao, Ying
Wu, Huimeng
Speakman, Scott A.
Hatton, T. Alan [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
metal-organic framework; chromium (III) terephthalate; phosphotungstic acid; Baeyer condensation; epoxidation; ONE-STEP SYNTHESIS; CARYOPHYLLENE OXIDE; HETEROGENEOUS CATALYST; EFFICIENT SYNTHESIS; BETA-NAPHTHOL; ACID; FACILE; SILICA; OXIDATION; PORE;
D O I
10.1021/cm2034382
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
Hybrid materials of the metal-organic framework (MOF), chromium(III) terephthalate (MIL-101), and phosphotungstic acid (PTA) were synthesized in aqueous media in the absence of hydrofluoric acid. XRD analysis of the MIL101/PTA composites indicates the presence of ordered PTA assemblies residing in both the large cages and small pores of MIL-101, which suggests the formation of previously undocumented structures. The MIL101/PTA structure enables a PTA payload 1.5-2 times higher than previously achieved. The catalytic performance of the MIL101/PTA composites was assessed in the Baeyer condensation of benzaldehyde and 2-naphthol, in the three-component condensation of benzaldehyde, 2-naphthol, and acetamide, and in the epoxidation of caryophyllene by hydrogen peroxide. The catalytic efficiency was demonstrated by the high (over 80-90%) conversion of the reactants under microwave-assisted heating. In four consecutive reaction cycles, the catalyst recovery was in excess of 75%, whereas the product yields were maintained above 92%. The simplicity of preparation, exceptional stability, and reactivity of the novel composites indicate potential in utilization of these catalytic matrices in a multitude of catalytic reactions and engineering processes.
引用
收藏
页码:1664 / 1675
页数:12
相关论文
共 75 条
[1]   The polyrner-supported sulfonic acid catalyzed one-step synthesis of diaminotriphenylmethanes [J].
An, Li-Tao ;
Ding, Fei-Qing ;
Zou, Han-Ping .
DYES AND PIGMENTS, 2008, 77 (02) :478-480
[2]  
[Anonymous], 1979, IONIZATION CONSTANTS
[3]   ISOMERIZATION OF CARYOPHYLLENE OXIDE CATALYZED BY SOLID ACIDS AND BASES [J].
ARATA, K ;
HAYANO, K ;
SHIRAHAMA, H .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1993, 66 (01) :218-223
[4]   Multicomponent, Solvent-Free Synthesis of 1-Amidoalkyl-2-naphthols in the Presence of H3+xPMo12-xVxO40 Heteropolyacids as Recyclable and Green Catalysts [J].
Bamoharram, Fatemeh F. ;
Heravi, Majid M. ;
Roshani, Mina ;
Charkhi, Mohammad J. Sane .
E-JOURNAL OF CHEMISTRY, 2011, 8 (02) :523-528
[5]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[6]   Silica supported perchloric acid (HClO4-SiO2):: A mild, reusable and highly efficient heterogeneous catalyst for the synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j]xanthenes [J].
Bigdeli, Mohammad A. ;
Heravi, Majid M. ;
Mahdavinia, Gholam Hossein .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2007, 275 (1-2) :25-29
[7]   Highly efficient separation of carbon dioxide by a metal-organic framework replete with open metal sites [J].
Britt, David ;
Furukawa, Hiroyasu ;
Wang, Bo ;
Glover, T. Grant ;
Yaghi, Omar M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (49) :20637-20640
[8]   THERMAL-ANALYSIS OF CHROMIUM(III) AND CHROMIUM(VI) SYSTEMS WITH SILICA AND SODIUM SILICATE [J].
BROWN, DH ;
FERGUSON, DA .
JOURNAL OF THERMAL ANALYSIS, 1976, 9 (01) :79-82
[9]   Mixed-component metal-organic frameworks (MC-MOFs): enhancing functionality through solid solution formation and surface modifications [J].
Burrows, Andrew D. .
CRYSTENGCOMM, 2011, 13 (11) :3623-3642
[10]   Metal Organic Framework MIL-101 for Adsorption and Effect of Terminal Water Molecules: From Quantum Mechanics to Molecular Simulation [J].
Chen, Y. F. ;
Babarao, R. ;
Sandler, S. I. ;
Jiang, J. W. .
LANGMUIR, 2010, 26 (11) :8743-8750