脱氢
化学
催化作用
金属
氮气
兴奋剂
产量(工程)
解放
化学工程
组合化学
有机化学
材料科学
冶金
工程类
生物化学
体外
光电子学
作者
Haitao Hu,Yuexing Zhang,Kaitlin A. Robinson,Yan‐Feng Yue,Renfeng Nie
标识
DOI:10.1016/j.apcatb.2022.121595
摘要
Metal-free carbocatalysts have sparked intensive interest in oxidative dehydrogenation. However, efficient metal-free carbocatalysts for non-oxidative dehydrogenation with H 2 liberation under mild conditions has rarely been reported. Herein, we successfully fabricated B,F co-doped nitrogen-assembly carbons (BF-NCs), which display outstanding catalytic performance and reaction generality in acceptorless dehydrogenation of N-heterocycles at mild and even at room temperatures, observably outperforming that of undoped NCs or single-doped B-NCs (B-NCs). Specifically, dual-active-sites were achieved in BF-NCs, i.e., the closely-placed graphitic nitrogen (CGN) and the pyridinic N banded BF x . The results of kinetic analysis and DFT directly reveal that the dual-active-sites on carbocatalysts lower the energy barriers for tetrahydroquinoline (THQ) dehydrogenation, thereby accelerating H 2 liberation even at room temperature. BF-NC shows promising recyclability and an ability to achieve 98.2% product yield without sacrificing efficacy in a 50-fold scale-up experiment, making the cost-effective and robust carbocatalysts a great contender for H 2 liberation in practical industrial application. Metal-free carbocatalyst with dual active sites, closely-placed graphitic nitrogen (CGN). and pyridinic N banded BFx, for acceptorless dehydrogenation of N-heterocycles at. ambient temperature, showing a greater activity than most reported carbocatalysts. • BF-NCs are fabricated by polymerization-carbonization strategy, followed by facial fluorination with HF. • BF-NCs are capable of base/oxidant-free dehydrogenation of various N-heterocycles at even ambient temperature. • High performance is directly owing to the presence of closely-spaced graphitic nitrogens and BF x as dual-active sites. • THQ is dehydrogenated to form labile C-H bonds, allowing BF-NCs to release molecular hydrogen without any H-acceptor. • BF-NCs show promising recyclability and high efficacy in a 50-fold scale-up experiment.
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