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Combining the advantages of 1,3,4-oxadiazole and tetrazole enables achieving high-energy insensitive materials.

Chao ZhangMei-Qi XuWen-Shuai DongZu-Jia LuHan ZhangXiao-Wei WuZhi-Min LiJian-Guo Zhang
Published in: Dalton transactions (Cambridge, England : 2003) (2023)
Combining the advantages of energetic heterocycles to achieve high-energy insensitive explosives is a significant challenge. Herein, based on high-energy tetrazole rings and highly stable 1,3,4-oxadiazole rings, a series of novel nitrogen rich energetic compounds 5-9 were successfully constructed. The related compounds were fully characterized by EA, FT-IR, NMR, DSC, and MS, and compounds 6-9 were further confirmed by X-ray single crystal diffraction. Among them, the energetic ion salts 6-8 show high thermal stability ( T dec > 250 °C) and low mechanical sensitivity (IS > 40 J, FS > 360 N), as well as good energy properties (7552-8050 m s -1 , 19.4-23.3 GPa). In particular, the azo compound 9 exhibits competent comprehensive performances ( T dec = 226.2 °C, D = 8502 m s -1 , P = 28.9 GPa, IS = 32 J, FS = 320 N). These results suggest that the strategy of integrating tetrazole and 1,3,4-oxadiazole and employing an azo structure as a bridging unit are effective approaches to construct high-energy insensitive materials.
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