Synthetic Strategies Toward Nitrogen-Rich Energetic Compounds Via the Reaction Characteristics of Cyanofurazan/Furoxan

被引:16
作者
Wang, Luoluo [1 ]
Zhai, Lianjie [1 ]
She, Weiqing [1 ]
Wang, Minchang [1 ]
Zhang, Junlin [1 ]
Wang, Bozhou [1 ]
机构
[1] Xian Modern Chem Res Inst, State Key Lab Fluorine & Nitrogen Chem, Xian, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2022年 / 10卷
基金
中国国家自然科学基金;
关键词
nitrogen-rich energetic compounds; cyanofurazan; furoxan; synthesis; reaction mechanism; energetic property; CRYSTAL-STRUCTURE; PERFORMANCE; AZO; SALTS; DENSITY; FURAZAN; HETEROCYCLES; CHEMISTRY; TETRAZOLE; BALANCE;
D O I
10.3389/fchem.2022.871684
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The structural units of amino-/cyano-substituted furazans and furoxans played significant roles in the synthesis of nitrogen-rich energetic compounds. This account focused on the synthetic strategies toward nitrogen-rich energetic compounds through the transformations based on cyanofurazan/furoxan structures, including 3-amino-4-cyanofurazan, 4-amino-3-cyano furoxan, 3,4-dicyanofurazan, and 3,4-dicyanofuroxan. The synthetic strategies toward seven kinds of nitrogen-rich energetic compounds, such as azo (azoxy)-bridged, ether-bridged, methylene-bridged, hybrid furazan/furoxan-tetrazole-based, tandem furoxan-based, hybrid furazan-isofurazan-based, hybrid furoxan-isoxazole-based and fused framework-based energetic compounds were fully reviewed, with the corresponding reaction mechanisms toward the nitrogen-rich aromatic frameworks and examples of using the frameworks to create high energetic substances highlighted and discussed. The energetic properties of typical nitrogen-rich energetic compounds had also been compared and summarized.
引用
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页数:23
相关论文
共 88 条
  • [11] Godovikova T.I., 2009, RUSS CHEM B+, V58, P406, DOI [10.1007/s11172-010-0023-5, DOI 10.1007/S11172-010-0023-5]
  • [12] GRUNDMANN C, 1975, LIEBIGS ANN CHEM, P1029
  • [13] Gem-dinitromethyl-substituted Energetic Metal-Organic Framework based on 1,2,3-Triazole from in situ Controllable Synthesis
    Gu, Hao
    Ma, Qing
    Huang, Shiliang
    Zhang, Zhenqi
    Zhang, Qi
    Cheng, Guangbin
    Yang, Hongwei
    Fan, Guijuan
    [J]. CHEMISTRY-AN ASIAN JOURNAL, 2018, 13 (19) : 2786 - 2790
  • [14] A good balance between the energy density and sensitivity from assembly of bis(dinitromethyl) and bis(fluorodinitromethyl) with a single furazan ring
    Guo, Tao
    Wang, Zijun
    Tang, Wang
    Wang, Wei
    Bi, Fuqiang
    Wang, Bozhou
    Zhou, Zhiming
    Meng, Zihui
    Ge, Zhongxue
    [J]. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2018, 134 : 218 - 230
  • [15] Boosting energetic performance by trimerizing furoxan
    He, Chunlin
    Gao, Haixiang
    Imler, Gregory H.
    Parrish, Damon A.
    Shreeve, Jean'ne M.
    [J]. JOURNAL OF MATERIALS CHEMISTRY A, 2018, 6 (20) : 9391 - 9396
  • [16] Nitrogen-Rich Tetrazolo[1,5-b]pyridazine: Promising Building Block for Advanced Energetic Materials
    Huang, Wei
    Tang, Yongxing
    Imler, Gregory H.
    Parrish, Damon A.
    Shreeve, Jean'ne M.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (07) : 3652 - 3657
  • [17] A DFT theoretical study of heats of formation and detonation properties of nitrogen-rich explosives
    Jaidann, Mounir
    Roy, Sandra
    Abou-Rachid, Hakima
    Lussier, Louis-Simon
    [J]. JOURNAL OF HAZARDOUS MATERIALS, 2010, 176 (1-3) : 165 - 173
  • [18] Bis(Nitroxymethylisoxazolyl) Furoxan: A Promising Standalone Melt-Castable Explosive
    Johnson, Eric C.
    Sabatini, Jesse J.
    Chavez, David E.
    Wells, Lucille A.
    Banning, Joseph E.
    Sausa, Rosario C.
    Byrd, Edward F. C.
    Orlicki, Joshua A.
    [J]. CHEMPLUSCHEM, 2020, 85 (01): : 237 - 239
  • [19] Safer and Convenient Synthesis of 3,4-Dicyanofuroxan
    Johnson, Eric C.
    Bukowski, Eric J.
    Sausa, Rosario C.
    Sabatini, Jesse J.
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2019, 23 (06) : 1275 - 1279
  • [20] SYNTHESIS OF 4,7-DIAMINOPYRIDAZINO[4,5-C]FUROXAN
    KHISAMUTDINOV, GK
    MRATKHUZINA, TA
    GABDULLIN, RM
    ABDRAKHMANOV, IS
    SMIRNOV, SP
    RAKITIN, OA
    GODOVIKOVA, TI
    KHMELNITSKII, LI
    [J]. RUSSIAN CHEMICAL BULLETIN, 1995, 44 (08) : 1499 - 1500