高桂萍. 钝感弹药及安全可靠起爆新技术[J].火炸药学报,1999, (2):63-66.GAO Gui-ping. Desensitive ammunition and new techniques of safe reliable initiation[J].Chinese Journal of Explosives and Propellants,1999,(2):63-66.
[2]
Reddy Damavarpu, Keerti Jayasuriya, Vladimiroff Theodore, et al. 2,4-dinitroimidazole:A less sensitive explosive and propellant made by thermal rearrangement of molten 1,4-dinitroimidazole[P].USP 5 387 297.
[3]
Bracuti A J. Molecular structure of a new potential propellant oxidizer 4,5- dinitroimidazole (45DNI) [J].Journal of Chemical Crystallography,1998, 28(5):367-371.
[4]
Jin Rai Cho, Soo Gyeong Cho, Kwang Joo Kim, et al. A candidate of new insensitive high explosive MTNI[A].Insensitive Munitions & Engergetic Materials Technology Symposium[C], 2000.393-400.
[5]
Behrens R, Land T A, Bulusu S. Decomposition, combustion and detonation chemistey of energetic materials[A].30th JANNAF Combustion Meeting[C],Materials Research Society, Boston, Mass,1996, vol. 418:111-117.
[6]
Urtiew P A, Tarver C M, Simpson R L. Shock initiation of 2,4-dinitroimidazole [R].DE 95017876,1995.
[7]
Hill L G, Seitz W L, Kramer J F,et al. Wedge test data for three new explosives:LAX112,2,4-DNI and TNAZ [R].DE 95016935,1995.
[8]
Bracuti A J. Crystal structure of 2,4-dinitroimidazole[J].Journal of Chemical Crystallography. 1995, 25:625.
[9]
Mary M Stinecipher, Michael D Coburn. Ammonium nitrate explosive systems[P].USP 4300962,1993.
[10]
李洪珍, 舒远杰, 黄奕刚. 3,3-二硝基氮杂环丁烷和1,1′-亚甲基-双(3,3-二硝基-1-氮杂环丁烷)的合成研究[J].有机化学,2004,24(7):775-777.LI Hong-zhen, SHU Yuan-jie, HUANG Yi-gang,et al. Study on the synthesis of 3,3-dinitro-azetidine and 1,1′-bis-(3,3-dinitroazetidin-1-yl) methane[J].Chinese Journal of Organic Chemistry, 2004,24(7):775-777.
[11]
张光全. 1,3,3-三硝基氮杂环丁烷(TNAZ)的工业合成现状及其应用进展[J].含能材料,2002,12(4):174-177.ZHANG Guang-quan. Technological synthecis and application advance of 1,3,3-trinitroazetidine (TNAZ) [J].Hanneng Cailiao, 2002,12(4):174-177.
[12]
Laali K K, Tanaka M, Forohar F, et al. Facile one-pot fluorination of polycyclic aromatic hydrocarbons (PAHs) with N-fluoro-2,4-dinitroimidazole;scope and limitation[J]. J Fluor Chem,1998, 91:185-190.
[13]
Lancini G C, Maggi N, Sensi P. Synthesis of some derivatives of 2-nitroimidazole with potential anti-trichomonas actity[J].Ed Sci,1963,18:390-396.
[14]
Grigoreva Valentina N, Fassakhov Rafael KH,Gafarow Ajrat N, et al. Method of Producing 1,4-Dinitroimidazoles[P].Su 1416488,1988.
[15]
Jerzy Suwinski, Ewa Salwinska. Nitroimidazoles, part IX some reactions of 1,4-DNI′s[J].Pol J Chem,1987,61(7-12):613-920.
[16]
M. Ross Grimmett, Sio-Tiok Hua, Kuei-Choo Chang, et al. 1,4-Dinitroimidazole and derivatives.structure and thermal rearrangement[J].Aust J Chem,1989.42(8):1281-1289.
[17]
Sharni G P, Fassakhov R Kh, Orlov P P. 2,4(5)-Dinitroimidazole[P].USSR 458553,1975.
[18]
Bhaumik K, Akamanchi K G. 2,4-dinitroimidazole:Microwave assisted synthesis and use in synthesis of 2,3-dihydro-6-nitroimidazo[2,1-b]oxazole analogues with antimycobacterial activity[J].Journal of Heterocyclic Chemistry, 2004,(1):51-55.
[19]
Vladimiroff T. Acidity and basicidity of nitro substituted imidazoles-technical rept [R].ADA 2939969,1995.
[20]
Minier L, Behrens R Fr, Bulu su S. Solid-phase thermal decomposition of 2,4-dinitroimidazole[R].DE 96003235,1996.
[21]
Behrens R,Minier L Bulusu.Coupling experimental dada and a prototype model to probe the physical and chemical processes of 2,4-dinitromimdazole solid-phase thermal decomposition [R].DE 98051315,1998.
