硝基苯
苯胺
试剂
水合物
联氨(抗抑郁剂)
无机化学
化学
氧化铜
氧化物
氧气
金属
离解(化学)
铜
X射线光电子能谱
还原剂
有机化学
物理化学
催化作用
化学工程
工程类
色谱法
作者
K. Rajendran,Pandurangan Nanjan,C. P. Vinod,Tuhin Suvra Khan,Shelaka Gupta,M. Ali Haider,Dinesh Jagadeesan
标识
DOI:10.1016/j.apcatb.2021.120417
摘要
Copper oxide (CuO) is used as a reusable solid reagent for hydrogenation of nitroarenes to aminoarenes. The use of CuO resulted in 100 % conversion of 2.9 mmol of nitrobenzene to aniline in 45 s at room temperature using hydrazine hydrate as the reducing agent. During the reaction, CuO is converted to inactive metallic Cu which can be regenerated to active CuO by thermal oxidation. DFT simulations indicated facile formation of oxygen vacancies (EO,vac = −3.8 kJ/mol) on the surface of CuO (111) in reducing environment which is consistent with the XPS analysis. Oxygen vacancies facilitate stronger nitrobenzene binding (−148.5 kJ/mol) and reduced activation barrier (Ea = 36.4 kJ/mol) for NO dissociation. Motivated from this mechanistic insight -NO2 groups in various nitroarenes were selectively hydrogenated to NH2 groups using CuO.
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