Metal-organic framework-derived cobalt nanoparticles modified nitrogen-doped porous carbon hybrids for efficient hydrogenation and one-pot reductive acetylation of nitroarenes

被引:2
作者
Luo, Peng [1 ,2 ]
Chen, Junteng [1 ,2 ]
Mu, Manman [1 ,2 ]
机构
[1] Tianjin Univ Technol, Sch Chem & Chem Engn, Tianjin 300384, Peoples R China
[2] Tianjin Key Lab Organ Solar Cells & Photochem Conv, Tianjin 300384, Peoples R China
关键词
Metal-organic framework; Metallic cobalt; N-doped porous carbon; Catalytic hydrogenation; One-pot reductive acetylation; CHEMOSELECTIVE HYDROGENATION; CATALYSTS; NANOCOMPOSITES; IMINES;
D O I
10.1007/s11144-023-02532-7
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
Herein, a series of cobalt nanoparticles embedded in nitrogen-doped porous carbon catalyst (Co@NPC) was prepared through the pyrolysis of tetragonal Co-based metal-organic framework which consisted of Co centers and benzimdazole linkers. Due to large BET specific surface area (389.41 m2/g), abundant metallic Co content (39.3%), small Co nanoparticle size and high pyridinic-N content, the as-obtained Co@NPC-700 catalyst exhibited superior catalytic performance for the hydrogenation and one-pot reductive acetylation of nitrobenzene. The high 99.80% conversion of nitrobenzene and 99.56% yield of aniline were acquired in the catalytic hydrogenation of nitrobenzene with hydrazine hydrate at 80 degrees C for 2 h. Simultaneously, the above catalyst showed high conversion (87.2%) and selectivity (95.3%) for the one-pot reductive acetylation of nitrobenzene in the presence of phenyl silane at room temperature. Additionally, Co@NPC-700 exhibited excellent activities for the catalytic hydrogenation and one-pot reductive acetylation of other nitroarenes as well as good recyclability. This work offered a facile approach to prepare metallic Co loaded on porous carbons, serving as efficient catalysts for catalytic reductive applications.
引用
收藏
页码:195 / 208
页数:14
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