电化学高效合成两种偶氮能化合物

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC
Synlett Pub Date : 2024-03-27 DOI:10.1055/a-2283-5829
Jinhao Zhang, Yulan Song, Wenjia Hao, Rufang Peng, Bo Jin
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引用次数: 0

摘要

具有高密度、高热值和优异引爆性能的偶氮化合物受到越来越多的研究关注。传统的化学脱氢法生成偶氮化合物需要使用强氧化剂,造成环境污染。电化学有机合成被认为是一种古老的方法和新技术。在这项工作中,偶氮呋咱四氮唑 {H2AzFT;5,5′-[重氮-1,2-二基双(1,2,5-恶二唑-4,3-二基)]双-1H-四氮唑}和偶氮呋咱羟基四氮唑(H2AzFTO)分别通过 5-(4-氨基呋咱-3-基)-1H-四氮唑和 5-(4-氨基呋咱-3-基)-1-羟基四氮唑的绿色高效电化学脱氢偶联合成。通过红外光谱、核磁共振和元素分析对 H2AzFT 和 (NH4)2AzFTO 的结构进行了全面表征,并通过差热分析确定了它们的热稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electrochemical Efficient Synthesis of Two Azo Energetic Compounds

Electrochemical Efficient Synthesis of Two Azo Energetic Compounds

Azo compounds with a high density, high enthalpy, and excellent detonation performance have received increasing research attention. The conventional method of chemical dehydrogenation that is used to form azo compounds involves the use of strong oxidants, resulting in environmental pollution. Electrochemical organic synthesis is considered an old method and a new technology. In this work, azofurazan tetrazole {H2AzFT; 5,5′-[diazene-1,2-diylbis(1,2,5-oxadiazole-4,3-diyl)]bis-1H-tetrazole} and azofurazan hydroxytetrazole (H2AzFTO) were synthesized by a green and efficient electrochemical dehydrogenation coupling of 5-(4-aminofurazan-3-yl)-1H-tetrazole and 5-(4-aminofurazan-3-yl)-1-hydroxytetrazole, respectively. The structures of H2AzFT and (NH4)2AzFTO were fully characterized by infrared spectroscopy, nuclear magnetic resonance, and elemental analysis, and their thermal stabilities were determined by differential thermal analysis.

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来源期刊
Synlett
Synlett 化学-有机化学
CiteScore
3.40
自引率
5.00%
发文量
369
审稿时长
1 months
期刊介绍: SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.
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