甲苯衍生物在水(H2O)和氨(NH3)催化下电化学转化为芳香族腈

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Sander Spittaels, Jef Vanhoof, Dirk E. De Vos
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引用次数: 0

摘要

芳香族腈是一种广泛生产的化学品,具有广泛的用途。这些化合物的高需求证明了寻找使用可再生能源的可持续合成替代品的合理性。本文报道了甲苯和二甲苯衍生物在常温条件下,用NH3和H2O在一锅两步法中电化学氧化生成芳香腈的过程。在第一步中,甲苯衍生物在没有催化剂的情况下被氧化为醛。第二步,加入氨和LiI作为电催化剂得到腈。采用对照实验和循环伏安法对反应网络和机理进行了研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrochemical Conversion of Toluene Derivatives to Aromatic Nitriles Using Water (H2O) and Ammonia (NH3)

Electrochemical Conversion of Toluene Derivatives to Aromatic Nitriles Using Water (H2O) and Ammonia (NH3)

Aromatic nitriles are extensively produced chemicals with a wide variety of applications. The high demand of these compounds justifies the search for sustainable synthesis alternatives using renewable energy. Here, an electrochemical oxidation of toluene and xylene derivatives to aromatic nitriles using NH3 and H2O under ambient conditions in a one-pot, two-step protocol is reported. In a first step, the toluene derivative is oxidized in the absence of a catalyst to the aldehyde. In the second step, ammonia is added together with LiI as an electrocatalyst to obtain the nitrile. The reaction network and mechanism are investigated using control experiments and cyclic voltammetry.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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