Controllable synthesis of carbon encapsulated iron phosphide nanoparticles for the chemoselective hydrogenation of aromatic nitroarenes to anilines

被引:31
作者
Zhu, Yanan [1 ,2 ]
Yang, Shuliang [1 ]
Cao, Changyan [1 ,2 ]
Song, Weiguo [1 ,2 ]
Wan, Li-Jun [1 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Lab Mol Nanostruct & Nanotechnol, CAS Res Educ Ctr Excellence Mol Sci,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; OXYGEN REDUCTION REACTION; EVOLUTION REACTION; HIGH-PERFORMANCE; FUNCTIONALIZED NITROARENES; SELECTIVE HYDROGENATION; CATALYSTS; EFFICIENT; ELECTROCATALYST; NANOMATERIALS;
D O I
10.1039/c7qi00803a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Selective hydrogenation of nitroarenes is an important chemical transformation to obtain functionalized anilines as key intermediates for pharmaceuticals and fine chemicals. Compared to the well-studied noble metal catalysts, heterogeneous catalysts based on low-cost transition metals are rarely reported. In this study, we developed an efficient and controllable route to synthesize a new kind of heterogeneous catalyst of iron phosphide nanoparticles encapsulated in a doped carbon matrix for the chemoselective hydrogenation of aromatic nitroarenes to anilines. Making use of the chemical reaction between Fe atoms in a MIL-88B-NH2 core and phosphorus atoms in a poly(cyclotriphosphazene-co-4,4-sulfonyldiphenol) (PZS) shell, iron phosphide nanoparticles encapsulated in a doped carbon matrix were successfully prepared through direct calcinations of a Fe-MOF@PZS core@shell precursor at 900 degrees C for 2 h under an Ar atmosphere. Due to the relative high surface area and porous structure as well as small nanoparticles, the prepared catalyst showed high catalytic activity, excellent selectivity and recyclability for the hydrogenation of aromatic nitroarenes to anilines.
引用
收藏
页码:1094 / 1099
页数:6
相关论文
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