Synthesis and Properties of Two 1,2,5-Oxadiazole based Energetic Salts with Nitrogen-Rich Fused Ring Skeleton

被引:0
|
作者
Li T. [1 ]
Yi W.-B. [1 ]
Yu Q. [1 ]
机构
[1] School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing
基金
中国国家自然科学基金;
关键词
crystal structure; energetic salts; nitrogen-rich fused ring; oxadiazole; properties; pyrazine; triazole;
D O I
10.11943/CJEM2024039
中图分类号
学科分类号
摘要
Two nitrogen-rich energetic salts,5,5′- (hydrazine-1,2-diyl)bis(5,7-dihydro- [1,2,5]oxadiazolo[3,4-e][1,2,4]tri- azolo[4,3-a]pyrimidine-8(4H)-one)perchlorate(2)and 5,5′- (diazene-1,2-diyl)bis([1,2,5]oxadiazolo[3,4-e][1,2,4]triazolo[4,3-a]pyrimidine-8(7H)-one)nitrate(3)were accomplished from the raw material of 5,6-diamino- [1,2,5]oxadiazolo[3,4-b]pyrazine(1). Structure characterization of energetic ionic salts 2 and 3 were achieved through various techniques,including Nuclear Magnetic Resonance Spectroscopy (NMR),Fourier Transform infrared spectroscopy (FTIR),elemental analysis (EA)and X-ray single crystal diffraction(XRD). Their thermal decomposition behaviors were investigated using differential scan - ning calorimetry(DSC)method,while their friction and impact sensitivities were identified according to BAM standard test meth - ods. Moreover,their detonation performances were predicted based on the combination of Isodesmic Reactions and EXPLO 5 software. The results prove that compounds 2 and 3 crystallize in the monoclinic system,belonging to space groups Pn and P21/n,respectively. The cationic parts of their crystal structures show good planarity and intensive hydrogen bonds in the crystal packing are observed. The thermal decomposition temperatures of compounds 2 and 3 are 154 ℃ and 130 ℃,respectively. Their theoretical detonation velocities are 7722 m·s-1 and 8008 m·s-1,while their theoretical detonation pressures are 26.3 GPa and 28.4 GPa,respectively. Their friction sensitivities are both 360 N,and impact sensitivities are greater than 40 J. Compounds 2 and 3 outperform traditional explosives TNT in terms of detonation performance,friction sensitivity,and impact sensitivity. © 2024 Institute of Chemical Materials, China Academy of Engineering Physics. All rights reserved.
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页码:615 / 622
页数:7
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共 31 条
  • [1] ZHANG J, ZHANG Q, THAO T, Et al., Energeticsalts with π-stacking and hydrogen-bonding interactions lead the way to future energetic materials[J], Journal of the American Chemical Society, 137, 4, pp. 1697-1704, (2015)
  • [2] YIN P, PARRISH D A, SHREEVE J M,, Et al., Energetic multi-functionalized nitraminopyrazoles and their ionic derivatives:Ternary hydrogen-bond induced high energy density materials [J], Journal of the American Chemical Society, 137, 14, pp. 4778-4786, (2015)
  • [3] ZHOU Yi-fei, WANG Tao, WANG Qiu-xiao, Et al., Progress in the study of energy-containing ionic salts containing nitrosa-mines[J], Chinese Journal of Energetic Materials (Hanneng Cailiao), 26, 11, pp. 967-982, (2018)
  • [4] CHAVEZ D E, BOTTARO J C,, PETRIE M,, Et al., Synthesis and thermal behavior of a fused,tricyclic 1,2,3,4 - tetrazine ring system[J], Angewandte Chemie International Edition, 127, 44, pp. 13165-13167, (2015)
  • [5] BENNETT A J,, FOROUGHI L M,, MATZGER A J,, Et al., Perchlorate-free energetic oxidizers enabled by ionic crystallization[J], Journal of the American Chemical Society, 146, 3, pp. 1771-1775, (2024)
  • [6] SHANG Y,, JIN B, PENG R,, Et al., A novel 3D energetic MOF of high energy content:Synthesis and superior explosive performance of a Pb(ii)compound with 5,5′-bistetrazole-1,1′-di-olate[J], Dalton Transactions, 45, 35, pp. 13881-13887, (2016)
  • [7] YIN P, ZHANG J, IMLER G H, Et al., Polynitro-functionalized dipyrazolo-1,3,5-triazinanes:Energetic polycyclization toward high density and excellent molecular stability[J], Angewandte Chemie International Edition, 56, 30, pp. 8834-8838, (2017)
  • [8] ZHANG J, ZHANG Q, VO T T,, Et al., Energetic salts with π-stacking and hydrogen-bonding interactions lead the way to future energetic materials[J], Journal of the American Chemical Society, 137, 4, pp. 1697-1704, (2015)
  • [9] HU L, YIN P,, ZHAO G,, Et al., Conjugated energetic salts based on fused rings:Insensitive and highly dense materials [J], Journal of the American Chemical Society, 140, 44, pp. 15001-15007, (2018)
  • [10] ZHANG J, SHREEVE J M., 3,3′-Dinitroamino-4,4′-azoxyfura-zan and its derivatives:An assembly of diverse N-O building blocks for high-performance energetic materials[J], Journal of the American Chemical Society, 136, 11, pp. 4437-4445, (2014)