纳米级 ZnO-NiO-Ni 异质结在醛与仲胺的可持续催化氨化中的协同作用

Amishwar Raysing Shelte, Rahul Daga Patil and Sanjay Pratihar
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引用次数: 0

摘要

金属-金属氢氧化物/氧化物界面催化剂因其具有多个活性位点而备受推崇,这些活性位点可在近距离内发生协同反应,从而实现先进的催化应用。在此,我们介绍一种通过涉及醛和仲胺的氧化酰胺化反应合成酰胺的高效且可持续的方法。该方法利用叔丁基过氧化氢(TBHP)作为氧化剂,在 90 °C 的四氢呋喃溶液中进行,并采用定义明确的氧化锌、氧化镍和镍的纳米级异质结 [ZnO-NiO-Ni] (ZN-O-A-7) 作为可回收的异质催化剂。氧化锌-氧化镍-镍异质结构及其协同作用对于提高氧化酰胺化反应的效率和选择性至关重要。该方法的多功能性在多种醛衍生物和仲胺(包括吗啉、硫代吗啉、哌嗪、吡咯烷和哌啶)中得到了验证。通过对照实验进行的机理研究深入了解了基本过程。该催化剂易于合成,只需使用一定量的氧化剂,具有极佳的选择性,对官能团的耐受性高,适用于各种醛和胺,可多次重复使用,并具有大规模工艺的潜力。这些特点共同提高了催化剂和方案的经济性和可持续性,为催化酰胺化反应领域做出了宝贵贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A cooperative nanoscale ZnO–NiO–Ni heterojunction for sustainable catalytic amidation of aldehydes with secondary amines†

A cooperative nanoscale ZnO–NiO–Ni heterojunction for sustainable catalytic amidation of aldehydes with secondary amines†

A cooperative nanoscale ZnO–NiO–Ni heterojunction for sustainable catalytic amidation of aldehydes with secondary amines†

Metal–metal hydroxide/oxide interface catalysts are valued for their multiple active sites, enabling synergistic reactions in close proximity for advanced catalytic applications. Herein, we present a highly efficient and sustainable method for synthesizing amides through oxidative amidation reactions involving aldehydes and secondary amines. The method utilizes tert-butyl hydroperoxide (TBHP) as the oxidant in THF at 90 °C and employs well-defined nanoscale heterojunctions of zinc oxide, nickel oxide, nickel [ZnO–NiO–Ni] (ZN-O-A-7) as a recyclable heterogeneous catalyst. The ZnO–NiO–Ni heterostructure and their synergistic cooperation are crucial for enhancing the efficiency and selectivity of the oxidative amidation reaction. The versatility of the methodology was demonstrated with diverse aldehyde derivatives and secondary amines, including morpholine, thiomorpholine, piperazine, pyrrolidine, and piperidine. Mechanistic investigations via controlled experiments provided insights into the underlying processes. The catalyst demonstrates ease of synthesis, use of stoichiometric amounts of oxidant, excellent selectivity, high functional group tolerance, applicability to various aldehydes and amines, multiple reusability, and potential for large-scale processes. These features collectively enhance the economic and sustainable nature of both the catalyst and the protocol, making a valuable contribution to the field of catalytic amidation reactions.

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