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基于三唑并呋咱化合物的新型共面双环化合物的合成、表征及性质

Synthesis, Characterization, and Properties of Novel Coplanar Bicyclic Compounds Based on Triazolofurazane Compounds.

作者信息

Xu Mei-Qi, Dong Wen-Shuai, Tariq Qamar-Un-Nisa, Zhang Chao, Li Cong, Lu Zu-Jia, Zhao Bin-Shan, Yu Qi-Yao, Zhang Jian-Guo

机构信息

State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, China.

出版信息

Molecules. 2025 Jun 29;30(13):2803. doi: 10.3390/molecules30132803.

DOI:10.3390/molecules30132803
PMID:40649318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12250748/
Abstract

In this study, a C-C bond-linked triazole-fused oxadiazole energetic compound, 4-amino-5-(4-amino-1,2,5-oxadiazol-3-yl)-2,4-dihydro-3-1,2,4-triazol-3-one (), was successfully designed and efficiently synthesized. Following nitration, a functional group-modified nitramine energetic compound () was obtained, and its energetic ionic salt () was further prepared. A comprehensive characterization of the structures of these three compounds was conducted, resulting in the successful elucidation of the single-crystal structures of compound ·Ca·6HO and compound ·MeOH. Compound exhibited a positive formation enthalpy (56.2 kJ·mol) and moderate mechanical sensitivity (FS = 120 N, IS = 12 J). Due to the presence of the nitramine group, compound 2 exhibited a relatively low thermal decomposition temperature ( = 94 °C). However, the thermal stability of compound was significantly improved ( = 233 °C), which is attributed to salt formation. Compound exhibits a positive formation enthalpy (121.0 kJ·mol), along with excellent detonation performance (D = 8120 m·s, P = 32.1 GPa) and reduced mechanical sensitivity (FS = 224 N, IS = 24 J). Therefore, the multi-heterocyclic compound, joined via C-C bond linkage, demonstrates outstanding performance, offering a new avenue for the design and synthesis of energetic materials.

摘要

在本研究中,成功设计并高效合成了一种碳 - 碳键连接的三唑稠合恶二唑含能化合物,4 - 氨基 - 5 -(4 - 氨基 - 1,2,5 - 恶二唑 - 3 - 基)- 2,4 - 二氢 - 3 - 1,2,4 - 三唑 - 3 - 酮()。硝化后,得到了一种官能团修饰的硝胺含能化合物(),并进一步制备了其含能离子盐()。对这三种化合物的结构进行了全面表征,成功解析了化合物·Ca·6H₂O和化合物·MeOH的单晶结构。化合物表现出正生成焓(56.2 kJ·mol⁻¹)和适度的机械感度(FS = 120 N,IS = 12 J)。由于硝胺基团的存在,化合物2表现出相对较低的热分解温度(Td = 94 °C)。然而,化合物的热稳定性显著提高(Td = 233 °C),这归因于盐的形成。化合物表现出正生成焓(121.0 kJ·mol⁻¹),以及优异的爆轰性能(D = 8120 m·s⁻¹,P = 32.1 GPa)和降低的机械感度(FS = 224 N,IS = 24 J)。因此,通过碳 - 碳键连接的多杂环化合物表现出优异的性能,为含能材料的设计与合成提供了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/cc683cce2ddc/molecules-30-02803-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/9194001b3646/molecules-30-02803-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/1f318674e4d4/molecules-30-02803-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/2c867a7e69ee/molecules-30-02803-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/37294c5eb0c1/molecules-30-02803-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/ef25ee2432f2/molecules-30-02803-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/e1426dd0ac7c/molecules-30-02803-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/1c610de001f3/molecules-30-02803-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/cc683cce2ddc/molecules-30-02803-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/9194001b3646/molecules-30-02803-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/1f318674e4d4/molecules-30-02803-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/2c867a7e69ee/molecules-30-02803-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/37294c5eb0c1/molecules-30-02803-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/ef25ee2432f2/molecules-30-02803-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/e1426dd0ac7c/molecules-30-02803-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/1c610de001f3/molecules-30-02803-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25c/12250748/cc683cce2ddc/molecules-30-02803-g007.jpg

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