CHINESE JOURNAL OF ENERGETIC MATERIALS
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4,4,8,8-四硝基-2,6-二氧杂金刚烷的合成及表征
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作者单位:

1.南京理工大学化工学院;2.南京工业大学化工学院

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基金项目:

国家自然科学基金(22075144)


Synthesis and Characterization of 4,4,8,8-Tetranitro-2,6-dioxaadamantane
Author:
Affiliation:

1.School of Chemistry and Chemical Engineering,Nanjing University of Science and Technology;2.College of Chemical Engineering, Nanjing Tech University

Fund Project:

Grant support: National Natural Science Foundation of China(No. 22075144)

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    摘要:

    以 9-氧杂双环[3.3.1]壬-2,6-二烯为原料经氧化环合、氧化、肟化、偕硝化四步反应合成了一种新型笼状含能化合物4,4,8,8-四硝基-2,6-二氧杂金刚烷。利用核磁共振、红外、元素分析对目标化合物进行了结构表征,通过X-射线单晶衍射确定了晶体结构,采用热重分析(TG)和差示扫描量热法(DSC)联用研究了热稳定性,通过EXPLO5预测了爆轰性能。结果表明,4,4,8,8-四硝基-2,6-二氧杂金刚烷的晶体密度为1.75 g·cm-3,属单斜晶系,P21/c空间群,起始分解温度为190.6 ℃,爆速为7705 m·s-1,爆压为25.75 GPa。

    Abstract:

    A novel cage-like energetic compound, 4,4,8,8-tetranitro-2,6-dioxaadamantane, was synthesized via four steps involving oxidative cyclization, oxidation, oximation and gem-dinitration by using 9-oxabicyclo[3.3.1]nona-2,6-diene as raw material. Its structure was characterized by nuclear magnetic resonance(NMR), Fourier transform infrared spectroscopy (FT‐IR) and elemental analysis (EA), and single crystal X-ray diffraction (SC-XRD)was adopted to further confirm its crystal structure. The thermal stability was investigated by differential scanning calorimetry‐thermogravimetry(DSC‐TG)analysis, and detonation parameters were predicted by EXPLO5. Results show that 4,4,8,8-tetranitro-2,6-dioxaadamantane has a crystal density of 1.75 g·cm-3 and belongs to monoclinic system, space groups P21/c. Its thermal decomposition temperature is 190.6 ℃, theoretical detonation velocity is 7705 m·s-1, and detonation pressure is 25.75 GPa.

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引用本文

李欢,周琪,侯天骄,等.4,4,8,8-四硝基-2,6-二氧杂金刚烷的合成及表征[J].含能材料, 2025, 33(6):557-564. DOI:10.11943/CJEM2025012.
LI Huan, ZHOU Qi, HOU Tian-jiao, et al. Synthesis and Characterization of 4,4,8,8-Tetranitro-2,6-dioxaadamantane[J]. Chinese Journal of Energetic Materials, 2025, 33(6):557-564. DOI:10.11943/CJEM2025012.

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  • 收稿日期: 2025-01-02
  • 最后修改日期: 2025-03-13
  • 录用日期: 2025-03-12
  • 在线发布日期: 2025-03-13
  • 出版日期: