4-Chloro-3,5-dinitropyrazole: a precursor for promising insensitive energetic compounds

被引:117
作者
He, Chunlin [1 ]
Zhang, Jiaheng [1 ]
Parrish, Damon A. [2 ]
Shreeve, Jean'ne M. [1 ]
机构
[1] Univ Idaho, Dept Chem, Moscow, ID 83844 USA
[2] USN, Res Lab, Washington, DC 20375 USA
关键词
REARRANGEMENT; PYRAZOLES; DESIGN; SALTS;
D O I
10.1039/c2ta01359b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of 3,5-dinitropyrazole derivatives was prepared from 4-chloro-3,5-dinitropyrazole in good yields and characterized by IR, H-1, and C-13 NMR (some cases N-15 NMR) spectroscopy, elemental analysis, and DSC. The structures of 7 and 13 were confirmed by single crystal X-ray diffraction. The impact sensitivity was determined using a standard BAM method, and detonation properties were obtained using experimental densities and calculated heats of formation.
引用
收藏
页码:2863 / 2868
页数:6
相关论文
共 45 条
[1]  
Agrawal J. P., 2010, High Energy Materials: Propellants, Explosives and Pyrotechnics, DOI DOI 10.1002/9783527628803
[2]  
[Anonymous], ANGEW CHEM, DOI DOI 10.1002/ange.200460366
[3]   1H,6H-triazolo[4,5-e]benzotriazole-3-oxides and 5,5′-(Z)diazene-1,2-diylbis(2-methyl-2H-1,2,3-benzotriazole) derived from chloronitrobenzotriazoles and hydrazine [J].
Carta, A ;
Piras, S ;
Boatto, G ;
Paglietti, G .
HETEROCYCLES, 2005, 65 (10) :2471-2481
[4]   A new synthesis of triazolo[4,5-g]quinolines and unexpected ring reduced products by treatment with hydrazine hydrate [J].
Carta, A ;
Paglietti, G .
ARKIVOC, 2004, :66-75
[5]   Quinoline tricyclic derivatives. Design, synthesis and evaluation of the antiviral activity of three new classes of RNA-dependent RNA polymerase inhibitors [J].
Carta, Antonio ;
Briguglio, Irene ;
Piras, Sandra ;
Corona, Paola ;
Boatto, Giampiero ;
Nieddu, Maria ;
Giunchedi, Paolo ;
Marongiu, Maria Elena ;
Giliberti, Gabriele ;
Iuliano, Filippo ;
Blois, Sylvain ;
Ibba, Cristina ;
Busonera, Bernardetta ;
La Colla, Paolo .
BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (23) :7070-7084
[6]  
Chavez DavidE., 2000, Angewandte Chemie, V112, P1861, DOI [DOI 10.1002/(SICI)1521-3757(20000515)112:103.0.CO
[7]  
2-B, DOI 10.1002/(SICI)1521-3757(20000515)112:10<1861::AID-ANGE1861>3.0.CO
[8]  
2-B]
[9]  
Chavez DE, 2000, ANGEW CHEM INT EDIT, V39, P1791, DOI 10.1002/(SICI)1521-3773(20000515)39:10<1791::AID-ANIE1791>3.0.CO
[10]  
2-9