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B,F Co-doped carbocatalysts with dual-active-sites for acceptorless dehydrogenation of N-heterocycles under room temperature

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
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:316: 121595-121595 被引量:2
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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