Journals / Turkish Journal of Chemistry / 2018 / Cilt: 42 - Sayı: 5

A new cocrystal explosive trinitrotoluene (TNT):1-amino-4-bromonaphthalene with reduced sensitivity

Pages
1321–1333
Publication Date
2018-10-11
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The results highlight that cocrystallization is an effective way to alter the impact sensitivity, detonation performance, decomposition temperature, melting point, oxygen balance, crystal packing, and the density of explosives.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A 1:1 cocrystal of TNT and 1-amino-4-bromonaphthalene was prepared via solvent evaporation.
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Key Findings & Data:Hirshfeld surfaces showed that these weak interactions were significant for crystal packing.
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Conclusion & Impact:The results highlight that cocrystallization is an effective way to alter the impact sensitivity, detonation performance, decomposition temperature, melting point, oxygen balance, crystal packing, and the density of explosives.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Trinitrotoluene · sensitivity · cocrystal

Abstract

A 1:1 cocrystal of TNT and 1-amino-4-bromonaphthalene was prepared via solvent evaporation. The structure of the cocrystal was determined via single-crystal and powder X-ray diffraction. Crystal structure determination studies indicated that the main mechanism of cocrystallization originates from the intermolecular hydrogen bonding (amino-nitro), halogen bonding, and π−ππ−π\pi -\pi stacking. Investigation of intermolecular interactions by Hirshfeld surface and fingerprint plot analysis revealed that the structures were stabilized by H...H, O...H, C...C (π−π)π−π)\pi -\pi ) and Br...O interactions. Hirshfeld surfaces showed that these weak interactions were significant for crystal packing. We analyzed the crystal packing and showed how this may influence sensitivity to impact. The TNT:1-amino-4-bromonaphthalene cocrystal displays significantly reduced impact sensitivity relative to pure TNT, indicating for the first time that a new TNT cocrystal was less sensitive to impact than pure TNT component. This difference in impact sensitivities may arise from the considerably different intermolecular interactions seen in the cocrystal structure. The results highlight that cocrystallization is an effective way to alter the impact sensitivity, detonation performance, decomposition temperature, melting point, oxygen balance, crystal packing, and the density of explosives.

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Cite This Article

ŞEN, N. (2018). A new cocrystal explosive trinitrotoluene (TNT):1-amino-4-bromonaphthalene with reduced sensitivity. Turkish Journal of Chemistry, Cilt: 42 - Sayı: 5, 1321–1333. https://ajindex.com/articles/184268

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References (25)

  1. Becuwe, A.; Delclos, A. Propellants, Explosives, Pyrotechnics. 1993, 18, 1-10.
  2. Van der Heijden, A. E. D. M.; Bouma, R. H. B.; Van der Steen, A. C. Propellants, Explosives, Pyrotechnics 2004, 29, 304-313.
  3. Millar, R. W.; Philbin, S. P.; Claridge, R. P.; Hamid, J. Propellants, Explosives, Pyrotechnics 2004, 29, 81-92.
  4. Zhurova, E. A.; Zhurov, V. V.; Pinkerton, A. A. J. Am. Chem. Soc. 2007, 129, 13887-13893.
  5. Sikder, A. K.; Sikder, N. J. Hazard. Mat. 2004, 112, 1-15.
  6. Shen, J. P.; Duan, X. H.; Luo, Q. P.; Zhou, Y.; Bao, Q.; Ma, Y. J.; Pei, C. H. Cryst. Growth Des. 2011, 11, 1759-1765.
  7. Remenar, J. F.; Morissette, S. L.; Peterson, M. L.; Moulton, B.; MacPhee, J. M.; Guzman, H. R.; Almarsson. J. Am. Chem. Soc. 2003, 125, 8456-8457.
  8. Weyna, D. R.; Shattock, T.; Vishweshwar, P.; Zaworotko, M. J. Cryst. Growth Des. 2009, 9, 1106-1123.
  9. Almarsson, Ö.; Zaworotko, M. J. Chem. Commun. 2004, 7, 1889-1896.
  10. Zhu, W.; Xiao, J.; Zhao, F.; Ji, G., Ma, X., Xiao, H. Acta Chim. Sin. 2007, 65, 1223. Wei, C.; Huang, H.; Duan, X.; Pei, C. Propellants, Explosives, Pyrotechnics 2004, 29, 81-92.
  11. Landenberger, K. B.; Matzger, A. J. Cryst. Growth Des. 2012, 12, 3603-3609.
  12. Sun, T.; Xiao, J. J.; Liu, Q.; Zhao, F., Xiao, H. M. J. Mater. Chem. A 2014, 2, 13898-13904.
  13. Bolton, O.; Matzger, A. J. Angew. Chem. 2011, 50, 8960-8963.
  14. Nguyen, K. L.; Friščić, T.; Day, G. M.; Gladden, L. F.; Jones, W. Nat. Mater. 2007, 6, 206-209.
  15. Alshahateet, S. F. J. Chem. Crystallogr. 2011, 41, 276-279.
  16. Klapötke, T. M. Chemistry of High-Energy Materials; Walter de Gruyter GmbH & Co. KG: Berlin:, Germany, 2011, p. 20. Landenberger, K. B.; Matzger, A. J. Cryst. Growth Des. 2010, 10, 5341-5347.
  17. Wang, Y; Yang, Y; Li, H; Zhou, Xi; Zhang, Qi; Wang, Ji; Liu, Y. Propellants, Explosives, Pyrotechnics 2014, 39, 590-596. Trzciński, W. A.; Cudziło, S.; Dyjak, S.; Nita, M. Cent. Eur. J. Energ. Mat. 2014, 11, 443-455.
  18. Zhang, H; Guo, C; Wang, Xi; Xu, J.; He, X.; Li, Y; Liu, X; Huang, H; Sun. J. Cryst. Growth Des. 2013, 13, 679-687.
  19. Loschen, C.; Klamt, A. Ind. Eng. Chem. Res. 2012, 51, 14303-14308.
  20. Hirsch, K. A.; Wilson, S. R.; Moore, J. S. J. Chem. Eur. 1997, 3, 765-771.
  21. Amabilino, D. B.; Stoddart, J. F. Chem. Rev. 1995, 95, 2725-2828.
  22. Ma, Y.; Zhang, A.; Xue, X.; Jiang, D.; Zhu, Y.; Zhang, C. Cryst. Growth Des. 2014, 14, 6101-6114.
  23. Brill, T. B.; James, K. J. Chem. Rev. 1993, 93, 2667-2692.
  24. Yang, Y. C.; Baker, J. A.; Ward, J. R. Chem. Rev. 1992, 92, 1729-1743.
  25. Ma, Y