Alexander A D, Thomas M K, Franz A M, et al.Nitraminoazoles based on ANTA-a comprehendsive study of structural and energetic properties[J].European Journal of Inorganic Chemistry, 2012: 2429-2443.
[2]
李加荣.唑系含能化合物的特征[J].火炸药学报, 1998(1): 56-57.LI Jia-rong.Properties of azoles energetic compounds[J].Chinese Journal of Explosives & Propellants, 1998(1): 56-57.
[3]
Pevzner M S, Kofman T P, Kibasova E N, et al.Reaction of 1-substituted 3,5-dinitro-1,2,4-triazoles with anions of heterocyclic acids[J].Khimiya Geterotsiklicheskikh Soedinenii, 1980(2): 257-261.
[4]
廉鹏, 来蔚鹏, 王伯周, 等.新型高能量密度化合物3,6-双(3,5-二硝基-1,2,4-三唑-1)-1,2,4,5-四嗪-1,4-二氧化物的性能预估及合成路线设计[J].化学学报, 2009,67(20): 2343-2348.LIAN Peng, LAI Wei-peng, WANG Bo-zhou, et al.Design of synthetic route and prediction of properties for a novel high energetic density compound 3,6-bis(3,5-dinitro-1,2,4- triazol-1-yl)-1,2,4,5-tetrazine-1,4- dioxide[J].Acta Chimica Sinica, 2009,67(20): 2343-2348.
[5]
Frisch M J, Trucks G W, Schlegel H B, et al.Gaussian 09[CP] Gaussian, Inc, Wallingford CT, 2009.
[6]
ZHANG Rui-zhou,LI Xiao-hong,ZHANG Xian-zhou.Theoretical studies on a series of 1,2,4-triazoles derivatives as potential high energy density compounds[J].Journal of Chemical Sciences, 124(5): 995-1006.
[7]
Bulat F A, Toro-Labbé A, Brinck T.Quantitative analysis of molecular surfaces: areas, volumes, electro -static potentials and average local ionization energies[J].J Mol Model, 2010,16(11): 1679-1691.
[8]
Politzer P, Murray J S.Relationships between lattice energies and surface electrostatic potentials and areas of anions[J].Journal of Physical Chemistry A, 1998,102(5): 1018-1020.
[9]
肖鹤鸣, 许晓娟, 邱玲.高能量密度材料的理论设计[M].北京: 科学出版社, 2008: 19-38.XIAO He-ming, XU Xiao-juan, QIU Ling.Theoretical design of high energy density materials[M].Beijing: Chinese Science Press, 2008: 19-38.
[10]
Rajendra P S, Hai xiang Gao, Dayal T M.Nitrogen-rich heterocycles[J].Struct Bond, 2007,125:35-83.
[11]
Kofman T P.Heterylation of 3-R1-5-R-1,2,4-triazoles with derivatives of 3,5-dinitro-1,2,4-triazole[J].Russian Journal of Organic Chemistry, 2001,37(8): 1158-1168.
[12]
Bottaro J C, Petric M A, Penwell P E, et al.NANO/HEDM technology: late stage exploratory effort[R].Report No.A466714,2003.
[13]
Klaptke T M, Piercey D G, Stierstorfer J.Amination of energetic anions: high-performing energetic materials[J].Dalton Transactions, 2012,41: 9451-9459.
[14]
Edward E G, Kenneth T R.N-amination and subsequent oxidation of some fused imidazoles and triazo -les[J].Journal of the Chemical Society, 1976,4: 367-371.
[15]
贺云, 范桂娟, 张光全, 等.1-氨基-3,5-二硝基-1,2,4-三唑的合成工艺改进及性能[J].含能材料, 2014,22(2): 182-185.HE Yun, FAN Gui-juan, ZHANG Guang-quan, et al.Synthesis improvement and properties of 1-amino-3,5-dinitro -1,2,4-triazole[J].Chinese Journal of Energetic Materials(Hanneng Cailiao), 2014,22(2): 182-185.
[16]
Lee K, Storm C, Hiskey M, et al.An improved synthesis of 5-amino-3-nitro-1H-1,2, 4-triazole (ANTA), A useful intermediate for the preparation of insensitive high explosives[J].Journal of Energetic Materials, 1991,9(5): 425-428．
[17]
贺云, 黄明 .5-氨基-3-硝基-1,2,4-三唑的合成及反应性研究进展[J].含能材料, 2012,20(6): 715-720.HE Yun, HUANG Ming, et al.Study on the synthesis and reactivity of 5-amino-3-nitro-1,2,4-trizole[J].Chinese Journal of Energetic Materials(Hanneng Cailiao), 2012,20(6): 715-720.
[18]
ZHOU Hua, MA Zhong-liang, WANG Jian-long, et al.Theoretical study of an energetic material di-1H-1,3,4-triazole derivatives[J].Defence Technology, 2014(10): 384-392.
[19]
马卿, 王军, 张晓玉.2,4,6-三甲基苯磺酰羟胺的合成与性能[J].含能材料, 2013,21(1): 133-134.MA Qin, WANG Jun, ZHANG Xiao-yu.Synthesis and performance of O-mesitylenesulfonyl hydroxylamine[J].Chinese Journal of Energetic Materials(Hanneng Cailiao), 2013,21(1): 133-134.
[20]
Kamlet M J, Jacobs S J.Chemistry of detonation.I.a simple method for calculating detonation properties of C,H,N,O explosives[J].The Journal of Chemical Physics, 1968,48: 23-35.
