硝基甲基取代的联四唑含能化合物合成及性能OA
Synthesis and Characterization of Nitromethyl-Substituted Bitetrazole Energetic Compounds
联四唑因氮含量超80%且拥有优异的爆轰性能,成为含能材料领域的研究重点,但其稳定性欠佳的问题严重制约了实际工程应用.本研究以5,5'-联四唑二铵盐为起始原料,通过亲核取代反应将溴代硝基甲烷连接到联四唑分子骨架上,成功合成出一种稳定性显著提升、可潜在应用于低共熔物的新型硝基甲基取代的联四唑含能化合物(1).采用核磁共振波谱(NMR)、元素分析(EA)和红外光谱(IR)完成了化合物1的结构表征,并通过单晶X射线衍射进一步确定其精确晶体结构.结果表明,化合物1属于单斜晶系,C2/c空间群,晶胞参数Z=8,晶体密度为1.683 g·cm-3,撞击感度为15 J、摩擦感度为324 N,计算爆速可达8325 m·s-1、计算爆压为28.4 GPa,综合性能优于传统炸药三硝基甲苯(TNT,爆速6881 m·s-1,爆压19.5 GPa,撞击感度15 J,摩擦感度353 N).
Bistetrazole has become a research focus in the field of energetic materials due to its 80%nitrogen content and excel-lent detonation performance.However,its poor stability seriously restricts practical engineering applications.In this work,5,5'-bistetrazole diammonium salt was used as the starting material,and bromonitromethane was grafted onto the bistetrazole skeleton via nucleophilic substitution reaction.A novel nitromethyl-substituted bistetrazole energetic compound 1 with signifi-cantly improved stability,which can be potentially used in eutectic systems,was successfully synthesized.The structure of compound 1 was characterized by nuclear magnetic resonance spectroscopy(NMR),elemental analysis(EA),and infrared spec-troscopy(IR).Its precise crystal structure was further determined by single-crystal X-ray diffraction:the compound crystallizes in the monoclinic system,space group C2/c,with cell parameter Z=8 and crystal density 1.683 g·cm-3.Performance test results show that compound 1 exhibits an impact sensitivity of 15 J,friction sensitivity of 324 N,detonation velocity of 8325 m·s-1,and detonation pressure of 28.4 GPa,demonstrating superior overall performance compared to TNT(Dv=6881 m·s-1,p=19.5 GPa,IS=15 J,FS=353 N).
余学治;程广斌;杨红伟
南京理工大学化学与化工学院,江苏 南京 210094南京理工大学化学与化工学院,江苏 南京 210094南京理工大学化学与化工学院,江苏 南京 210094
军事科技
含能化合物联四唑硝基甲烷爆轰性能
energetic compoundsbitetrazolenitromethanedetonation performance
《含能材料》 2026 (3)
229-234,6
国家自然科学基金(22538009,22505109),中国博士后科学基金(2024M764227,2023M741696)National Natural Science Foundation of China(Nos.22538009,22505109),China Postdoctoral Science Foun-dation(Nos.2024M764227,2023M741696)
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