Quinoxaline synthesis via oxidative cyclization reaction using metal-organic framework Cu(BDC) as an efficient heterogeneous catalyst

被引:58
作者
Dang, Giao H. [1 ]
Vu, Yen T. H. [1 ]
Dong, Quoc A. [1 ]
Le, Dung T. [1 ]
Thanh Truong [1 ]
Phan, Nam T. S. [1 ]
机构
[1] HCMC Univ Technol, Dept Chem Engn, VNU HCM, Ho Chi Minh City, Vietnam
关键词
Metal-organic framework; Oxidative cyclization; Quinoxaline Cu(BDC); Heterogeneous catalyst; ALPHA-HYDROXYKETONES; MOLECULAR-IODINE; DERIVATIVES; MOFS; NI-2(BDC)(2)(DABCO); CU-2(BPDC)(2)(BPY); NANOPARTICLES; ACTIVATION; ALKYLATION; CONVENIENT;
D O I
10.1016/j.apcata.2014.11.009
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 metal-organic framework Cu(BDC) was synthesized, and characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR), atomic absorption spectrophotometry (MS), and nitrogen physisorption measurements. The Cu(BDC) was employed as an efficient heterogeneous catalyst for the oxidative cyclization reaction between alpha-hydroxyacetophenone and phenylenediamine to form 2-phenylquinoxaline as the principal product. The optimal conditions involved the use of air atmosphere oxidant in toluene solvent at 100 degrees C in 3 h. In addition, the Cu(BDC) exhibited higher catalytic activity in the quinoxaline synthesis reaction than that of others Cu-MOFs such as MOE-199, MOF-118, and Cu-2(BDC)(2)(DABCO), and higher than that of Mn(BDC), and Ni-2(BDC)(2)(DABCO). The Cu(BDC) catalyst could be recovered and reused several times without a significant degradation in catalytic activity. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 79 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]   Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines [J].
Antoniotti, S ;
Duñach, E .
TETRAHEDRON LETTERS, 2002, 43 (22) :3971-3973
[3]   Metal-Organic Framework Thin Films: From Fundamentals to Applications [J].
Betard, Angelique ;
Fischer, Roland A. .
CHEMICAL REVIEWS, 2012, 112 (02) :1055-1083
[4]   An efficient protocol for the synthesis of quinoxaline derivatives at room temperature using molecular iodine as the catalyst [J].
Bhosale, RS ;
Sarda, SR ;
Ardhapure, SS ;
Jadhav, WN ;
Bhusare, SR ;
Pawar, RP .
TETRAHEDRON LETTERS, 2005, 46 (42) :7183-7186
[5]   Synthesis and Structure Characterization of Copper Terephthalate Metal-Organic Frameworks [J].
Carson, Cantwell G. ;
Hardcastle, Kenneth ;
Schwartz, Justin ;
Liu, Xiaotao ;
Hoffmann, Christina ;
Gerhardt, Rosario A. ;
Tannenbaum, Rina .
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2009, (16) :2338-2343
[6]   Metal-Organic Frameworks with Functional Pores for Recognition of Small Molecules [J].
Chen, Banglin ;
Xiang, Shengchang ;
Qian, Guodong .
ACCOUNTS OF CHEMICAL RESEARCH, 2010, 43 (08) :1115-1124
[7]   Copper-catalyzed oxidative cyclization of α-hydroxyketones with o-phenylenediamines leading to quinoxalines [J].
Cho, Chan Sik ;
Oh, Sung Gi .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2007, 276 (1-2) :205-210
[8]   A recyclable copper catalysis in quinoxaline synthesis from α-hydroxyketones and o-phenylenediamines [J].
Cho, Chan Sik ;
Ren, Wen Xiu .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2009, 694 (19) :3215-3217
[9]   MOFs as Multifunctional Catalysts: Synthesis of Secondary Arylamines, Quinolines, Pyrroles, and Arylpyrrolidines over Bifunctional MIL-101 [J].
Cirujano, Francisco G. ;
Leyva-Perez, Antonio ;
Corma, Avelino ;
Llabres i Xamena, Francesc X. .
CHEMCATCHEM, 2013, 5 (02) :538-549
[10]   Gold Catalysis Opens Up a New Route for the Synthesis of Benzimidazoylquinoxaline Derivatives from Biomass-Derived Products (Glycerol) [J].
Climent, Maria J. ;
Corma, Avelino ;
Iborra, Sara ;
Martinez-Silvestre, Sergio .
CHEMCATCHEM, 2013, 5 (12) :3866-3874