Fe-Based Metal-Organic Frameworks for Highly Selective Photocatalytic Benzene Hydroxylation to Phenol

被引:359
作者
Wang, Dengke [1 ]
Wang, Mengtao [1 ]
Li, Zhaohui [1 ]
机构
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
关键词
benzene hydroxylation; phenol; photocatalysis; Fe-based metal-organic framework; H2O2; VISIBLE-LIGHT PHOTOCATALYSIS; HYDROGEN-PEROXIDE; CO2; REDUCTION; OXIDATION; WATER; TRANSFORMATIONS; NANOPARTICLES; DEGRADATION; IRRADIATION; OXYGENATION;
D O I
10.1021/acscatal.5b01949
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
Phenol is one of the most important chemicals in industry. One-step selective benzene hydroxylation is an attractive yet challenging method for phenol production, especially when such a reaction can be driven by solar energy. Herein, we reported that a highly selective benzene hydroxylation to phenol can be achieved over two Fe-based metal organic frameworks [MIL-100(Fe) and MIL-68(Fe)] under visible light irradiations using hydrogen peroxide (H2O2) as an oxidant. An optimal benzene conversion of 30.6% was achieved with a H2O2:benzene ratio of 3:4 over MIL-100(Fe) after 24 h irradiations. ESR results and the kinetic studies suggested that a successful coupling of the photocatalysis of Fe-O clusters in Fe-based metal organic frameworks (MOFs) with a Fenton-like route is involved in this benzene hydroxylation process. The comparison of the reaction over MIL-100(Fe) and MIL-68(Fe) reveals that the structure of MOFs significantly influences the photocatalytic efficiency. Because the composition and the structure of MOFs are highly tunable, this study highlights the great potential of using Fe-based MOFs for photocatalytic benzene hydroxylation to form phenol, which may result in an economical, sustainable, and thus green process for phenol production.
引用
收藏
页码:6852 / 6857
页数:6
相关论文
共 50 条
[1]   Synergistic Effect between Ultrasmall Cu(II) Oxide and CuCr2O4 Spinel Nanoparticles in Selective Hydroxylation of Benzene to Phenol with Air as Oxidant [J].
Acharyya, Shankha Shubhra ;
Ghosh, Shilpi ;
Tiwari, Ritesh ;
Pendem, Chandrashekar ;
Sasaki, Takehiko ;
Bal, Rajaram .
ACS CATALYSIS, 2015, 5 (05) :2850-2858
[2]   Semiconductor behavior of a metal-organic framework (MOF) [J].
Alvaro, Mercedes ;
Carbonell, Esther ;
Ferrer, Belen ;
Llabres i Xamena, Francesc X. ;
Garcia, Hermenegildo .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (18) :5106-5112
[3]   Kinetics and mechanism of benzene derivative degradation with Fenton's reagent in aqueous medium studied by MIMS [J].
Augusti, R ;
Dias, AO ;
Rocha, LL ;
Lago, RM .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (52) :10723-10727
[4]   The control of selectivity in benzene hydroxylation catalyzed by TS-1: The solvent effect and the role of crystallite size [J].
Barbera, D. ;
Cavani, F. ;
D'Alessandro, T. ;
Fornasari, G. ;
Guidetti, S. ;
Aloise, A. ;
Giordano, G. ;
Piumetti, M. ;
Bonelli, B. ;
Zanzottera, C. .
JOURNAL OF CATALYSIS, 2010, 275 (01) :158-169
[5]  
Bianchi D, 2000, ANGEW CHEM INT EDIT, V39, P4321, DOI 10.1002/1521-3773(20001201)39:23<4321::AID-ANIE4321>3.0.CO
[6]  
2-5
[7]   THE SELECTIVE OXIDATION OF PRIMARY ALCOHOLS TO ALDEHYDES BY O-2 EMPLOYING A TRINUCLEAR RUTHENIUM CARBOXYLATE CATALYST [J].
BILGRIEN, C ;
DAVIS, S ;
DRAGO, RS .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (12) :3786-3787
[8]   Electro-Fenton Process and Related Electrochemical Technologies Based on Fenton's Reaction Chemistry [J].
Brillas, Enric ;
Sires, Ignasi ;
Oturan, Mehmet A. .
CHEMICAL REVIEWS, 2009, 109 (12) :6570-6631
[9]   Fe-g-C3N4-Catalyzed Oxidation of Benzene to Phenol Using Hydrogen Peroxide and Visible Light [J].
Chen, Xiufang ;
Zhang, Jinshui ;
Fu, Xianzhi ;
Antonietti, Markus ;
Wang, Xinchen .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (33) :11658-+
[10]   Luminescent Functional Metal-Organic Frameworks [J].
Cui, Yuanjing ;
Yue, Yanfeng ;
Qian, Guodong ;
Chen, Banglin .
CHEMICAL REVIEWS, 2012, 112 (02) :1126-1162