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Preparation and Characterization of Cationic Energetic Salts of 5-Amino-3-[(2,4,6-trinitrophenyl)amino]-1H-1,2,4-triazole (APATO)

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Języki publikacji
EN
Abstrakty
EN
The synthesis and properties of some 5-amino-3-[(2,4,6-trinitrophenyl) amino]-1H-1,2,4-triazole (APATO) cationic salts are described. A detailed structure of one of the salts obtained, 5-amino-3-[(2,4,6-trinitrophenyl)amino]-1H-1,2,4-triazol-4-ium perchlorate (APATO·HClO4) was characterized using low temperature (173 K) single crystal X-ray diffraction: orthorhombic yellow block, space group ‘Pbc21’, crystal density at 173 K (calculated) and at 293 K (pycnom.) were 1.863 and 1.840 g/cm3, respectively. The APATO salts were characterized by spectroscopic methods and thermal analysis. Preliminary computer calculated energetic characteristics showed that the synthesized salts possess increased energetic characteristics, superior in comparison to the TNT. The APATO perchlorate salt may deserve special attention as a thermostable HEDM.
Rocznik
Strony
311--325
Opis fizyczny
Bibliogr. 25 poz., rys., tab., wykr.
Twórcy
  • Institute of Biochemistry, Life Science Center, Vilnius University, Sauletekio av. 7, Vilnius, 10257 Lithuania
  • Institute of Theoretical Physics and Astronomy, Vilnius University, Sauletekio av. 3, Vilnius, 10222 Lithuania
Bibliografia
  • [1] Agrawal, J.P.; Hodgson, R. Organic Chemistry of Explosives. Wiley Interscience, N.Y., 2007; ISBN: 978-0-470-02967-1.
  • [2] Urbanski, T. Chemistry and Technology of Explosives. Warszawa, Vol. 1-4, 1964.
  • [3] Klapötke, T.M. Chemistry of High-Energy Materials. Walter de Gruyter, Berlin, 2012. pp. 141-142; ISBN 978-3110273588.
  • [4] Pagoria, P.F.; Lee, G.S.; Mitchell, A.R.; Schmidt, R.D. A Review of Energetic Materials Synthesis. Thermochim. Acta 2002, 384: 187-204; DOI: 10.1016/S0040-6031(01)00805-X.
  • [5] Coburn, M.D.; Harris, B.W.; Lee, K.-Y.; Stinecipher, M.M.; Heyden, H.H. Explosives Synthesis at Los Alamos. Ind. Eng. Chem. Prod. Res. Dev. 1986, 25: 68-72; DOI: 10.1021/i300021a015.
  • [6] Larsson, A.; Wingborg, N. Green Propellants Based on Ammonium Dinitramide (ADN). In: Advances in Spacecraft Technologies. (Hall, J., Ed.) InTech, Rijeka, Croatia, 2011, pp. 139-156; DOI: 10.5772/13640.
  • [7] Matyáš, R.; Pachman, J. Primary Explosives. Springer, Germany, 2013, pp. 212-226; ISBN: 978-3-642-28436-6.
  • [8] Liu, W.; Liu, W.L.; Pang, S.P. Structures and Properties of Energetic Cations in Energetic Salts. RSC Adv. 2017, 7: 3617-3627; DOI: 10.1039/C6RA26032B.
  • [9] Östmark, H.; Bemm, U.; Bergman, H.; Langlet, A. N-Guanylurea-Dinitramide: A New Energetic Material with Low Sensitivity for Propellants and Explosives Applications. Termochim. Acta 2002, 384: 253-259; DOI: 10.1016/S0040-6031(01)00800-0.
  • [10] Agrawal, J.P. Past, Present and Future of Thermally Stable Explosives. Cent. Eur. J. Energ. Mater. 2012, 9(3): 273-290.
  • [11] Ostrovskii, V.A.; Pevzner, M.S.; Kofman, T.P.; Tselinskii, I.V. Energetic 1,2,4-Triazoles and Tetrazoles: Synthesis, Structure and Properties. Targets Heterocycl. Syst. 1999, 3: 467- 526; ISBN 88-86208-13-8.
  • [12] Gao, H.; Shreeve, J.M. Azole-Based Energetic Salts (Review). Chem. Rev. 2011, 111(11): 7377-7436; DOI: 10.1021/cr200039c.
  • [13] Xue, H.; Gao, Y.; Twamley, B.; Shreeve, J.M. New Energetic Salts Based on Nitrogen-Containing Heterocycles. Chem. Mater. 2005, 17: 191-198; DOI: 10.1021/cm048864x.
  • [14] Green Energetic Materials. (Brinck, T., Ed.) Wiley, Chichester, UK, 2014, pp. 1-290; ISBN: 978-1-119-94129-3.
  • [15] Talawar, M.B.; Sivabalan, R.; Mukundan, T.; Muthurajam, H.; Sikder, A.K.; Gandhe, B.R.; Rao, A.S. Environmentally Compatible Next Generation Green Energetic Materials. J. Hazard. Mater. 2009, 161: 589-607; DOI: 10.1016/j.jhazmat.2008.04.011.
  • [16] Šarlauskas, J.; Nemeikaitė-Čėnienė, A.; Anusevičius, Ž.; Misevičienė, L.; Marozienė, A.; Markevičius, A.; Čėnas, N. Enzymatic Redox Properties of Novel Nitrotriazole Explosives: Implications for their Toxicity. Z. Naturforsh. 2004, 59(c): 399-404, DOI: 10.1515/znc-2004-5-620.
  • [17] Klapötke, T.M.; Sabaté, C.M.; Stierstorfer, J. Hydrogen-bonding Stabilization in Energetic Perchlorate Salts: 5-Amino-1H-tetrazolium Perchlorate and its Adduct with 5-Amino-1H-tetrazole. Z. Anorg. Allg. Chem. 2008, 634: 1867-1874; DOI: 10.1002/zaac.200800228.
  • [18] Thottempudi, V.; Shreeve, J.M. Synthesis and Promising Properties of a New Family of High-Density Energetic Salts of 5-Nitro-3-trinitromethyl-1H-1,2,4-triazole and 5,5′-Bis (trinitromethyl)-3,3′-azo-1H-1,2,4-triazole. J. Am. Chem. Soc. 2011, 133(49): 19982-19992; DOI: 10.1021/ja208990z.
  • [19] Chioato, Z.L.; Klapötke, T.M.; Mieskes, F.; Stierstörfer, J.; Weyrauther, M. (Picrylamino)-1,2,4-triazole Derivatives ‒Thermally Stable Explosives. Eur. J. Inorg. Chem. 2016, 7: 956-962; DOI: 10.1002/ejic.201501435.
  • [20] Wu, B.; Wang, Z.X.; Yang, H.W.; Lin, Q.H.; Ju, X.H.; Lu, C.X.; Cheng, G.B. Synthesis and Characterization of a New Family of Energetic Salts Based on a Guanidinium Cation Containing a Picryl Moiety. New J. Chem. 2015, 39: 893-901; DOI: 10.1039/C4NJ01849D.
  • [21] Panasiuk, O.H.; Shestozub, A.B. Salts of Polynitroaryl Derivatives of Some Substituted s-Triazoles. (in Ukrainian) Patent UA 7340, 2005.
  • [22] Coburn, M.D.; Jackson, T.E. Picrylamino‐substituted Heterocycles. III. 1,2,4‐Triazoles. J. Heterocycl. Chem. 1968, 5: 199-203; DOI: 10.1002/jhet.5570050208.
  • [23] Keshavarz, M.H.; Motamedoshariati, H.; Moghayadnia, R.; Nazari, H.R.; Azarniamehraban, J. A New Computer Code to Evaluate Detonation Performance of High Explosives and Their Thermochemical Properties. Part I. J. Hazard. Mater. 2009, 172: 1218-1228; DOI: 10.1016/j.jhazmat.2009.07.128.
  • [24] Šarlauskas, J.; Vaitekūnas, J.; Tamulienė, J. Energetic Polynitrophenyl Substituted 1,2,4-Triazole Derivatives: Synthesis, Properties and LC-MS Analysis. Proc. 21st Semin. New Trends Res. Energ. Mater., Pardubice, Czech Republic, 2018, 1080-1094; ISBN: 9788075601360.
  • [25] Yigiter, A.Ö.; Atakol, M.K.; Aksu, M.L.; Atakol, O. Thermal Characterization and Theoretical and Experimental Comparison of Picryl Chloride Derivatives of Heterocyclic Energetic Compounds. J. Therm. Anal. Cal. 2017, 127: 2199-2123; DOI: 10.1007/s10973-016-5766-2.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-5009354f-8f1b-4cc4-8a28-c7024e5c4091
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