Diagonally Compressed TNAZ - A DFT Treatment

  • Lemi Türker Department of Chemistry, Middle East Technical University, Üniversiteler, Eskişehir Yolu No: 1, 06800 Çankaya/Ankara, Turkey
Keywords: TNAZ, 1,3,3-trinitroazetidine, explosive, impact sensitivity, DFT

Abstract

TNAZ is an insensitive explosive material having a 4-membered azetidine ring system which has three nitro groups substituted, one of them is a nitramine type. In the present density functional treatise at the level of B3LYP/6-311++G(d,p), the 4-membered ring of TNAZ is compressed diagonally either along the X- or Y-axis direction. Various properties (including energies, quantum chemical and spectral etc.) in the perturbed systems have been searched and discussed.

References

P.F. Pagoria, G.S. Lee, R. A. Mitchell and R.D. Schmidt, A review of energetic materials synthesis, Thermochim. Acta 384 (2002), 187-204. https://doi.org/10.1016/S0040-6031(01)00805-X

H.S. Jadhav, M.B. Talawar, D.D. Dhavale, S.N. Asthana and V.V. Krishnamurthy, Alternate method to synthesis of 1,3,3-trinitroazetedine (TNAZ): Next generation melt castable high energy material, Indian J. Chemical Technology 13 (2006), 41-46.

L. Türker, A composite of NTO and TNAZ - A DFT treatment, Earthline Journal of Chemical Sciences 5(2) (2021) 261-274. https://doi.org/10.34198/ejcs.5221.261274

L. Türker, A DFT treatment of some aluminized 1,3,3-trinitroazetidine (TNAZ) systems - A deeper look, Earthline Journal of Chemical Sciences 3(2) (2020), 121-140. https://doi.org/10.34198/ejcs.3220.121140

T.G. Archibald, R. Gilardi, K. Baum and C.J. George, Synthesis and x-ray crystal structure of 1,3,3-trinitroazetidine, J. Org. Chem. 55 (1990), 2920-2924. https://doi.org/10.1021/jo00296a066

R.L. McKenney, Jr., T.G. Floyd, W.E. Stevens, T.G. Archibald, A.P. Marchand, G.V.M. Sharma and S.G. Bott, Synthesis and thermal properties of 1,3-dinitro-3-(1′,3′-dinitroazetidin-3′-yl) azetidine (TNDAZ) and its admixtures with 1,3,3-trinitroazetidine (TNAZ), J. Energ. Mater. 16 (1998), 199-235. https://doi.org/10.1080/07370659808217513

A.M. Hiskey, M.C. Johnson and E.D. Chavez, Preparation of 1-substituted-3,3-dinitroazetidines, J. Energ. Mater. 17 (1999), 233-252. https://doi.org/10.1080/07370659908216106

J. Zhang, R. Hu, C. Zhu, G. Feng and Q. Long, Thermal behavior of 1,3,3- trinitroazetidine, Thermochim. Acta 298 (1997), 31-35. https://doi.org/10.1016/S0040-6031(97)00056-7

S. Zeman, The thermoanalytical study of some amino derivatives of 1,3,5-trinitrobenzene, Thermochim. Acta 216 (1993), 157-168. https://doi.org/10.1016/0040-6031(93)80389-R

M.H. Keshavarz, Approximate prediction of melting point of nitramines, nitrate esters, nitrate salts and nitroaliphatics energetic compounds, J. Hazard. Mater. 138 (2006), 448-451. https://doi.org/10.1016/j.jhazmat.2006.05.097

Z. Jalovy, S. Zeman, M. Suceska, P. Vavra, K. Dudek and J.M. Rajic, 1,3,3- Trinitroazetidine (TNAZ). Part I. Syntheses and properties, J. Energ. Mater. 19 (2001), 219-239. https://doi.org/10.1080/07370650108216127

D.S. Watt and M.D. Cliff, Evaluation of 1,3,3-trinitroazetidine (TNAZ) – A high performance melt-castable explosive, Technical Report DSTO-TR-1000, Defence Science and Technology Organization (DSTO), Aeronautical and Maritime Research Laboratory, Melbourne, Australia, 2000.

A.K. Sikder and N. Sikder, A review of advanced high performance, insensitive and thermally stable energetic materials emerging for military and space applications, J. Hazard. Mater. 112 (2004), 1-15. https://doi.org/10.1016/j.jhazmat.2004.04.003

S. Iyer, E. Y. Sarah, M. Yoyee, R. Perz, J. Alster and D. Stoc, TNAZ based composition C-4 development, 11th Annual Working Group, Institute on Synthesis of High Density Materials (Proc.), Kiamesha Lakes, 1992.

M. Oftadeh, M. Hamadanian, M. Radhoosh and M.H. Keshavarz, DFT molecular orbital calculations of initial step in decomposition pathways of TNAZ and some of its derivatives with –F, –CN and –OCH3 groups, Computational and Theoretical Chemistry 964 (2011), 262-268. https://doi.org/10.1016/j.comptc.2011.01.007

J.O. Doali, R.A. Fifer, D.I. Kruzezynski and B.J. Nelson, The mobile combustion diagnostic fixture and its application to the study of propellant combustion Part-I. Investigation of the low pressure combustion of LOVA XM-39 Propellant, Technical Report No: BRLMR-3787/5, US Ballistic Research Laboratory, Maryland, 1989.

J.P. Agrawal, Recent trends in high-energy materials, Prog. Energ. Combust. Sci. 24/1 (1998), 1-30. https://doi.org/10.1016/S0360-1285(97)00015-4

M.D. Coburn, M.A. Hiskey and T.G. Archibald, Scale-up and waste-minimization of the Los Alamos process for 1,3,3-trinitroazetidine (TNAZ), Waste Management 17 (1997), 143-146. https://doi.org/10.1016/S0956-053X(97)10013-7

L. Jizhen, F. Xuezhong, F. Xiping, Z. Fengqi and H. Rongzu, Compatibility study of 1,3,3-trinitroazetidine with some energetic components and inert materials, Journal of Thermal Analysis and Calorimetry 85(3) (2006), 779-784. https://doi.org/10.1007/s10973-005-7370-8

L. Türker and S. Varis, Desensitization of TNAZ via molecular structure modification and explosive properties – A DFT study, Acta Chim. Slov. 59 (2012), 749-759.

J. Wu, Y. Huang, L. Yang, D. Geng, F. Wang, H. Wang and L. Chen, Reactive molecular dynamics simulations of the thermal decomposition mechanism of 1,3,3-trinitroazetidine, Chem. Phys. Chem. 19(20) (2018), 2683-2695. https://doi.org/10.1002/cphc.201800550

J.J.P. Stewart, Optimization of parameters for semiempirical methods I. Method, J. Comput. Chem. 10 (1989), 209-220. https://doi.org/10.1002/jcc.540100208

J.J.P. Stewart, Optimization of parameters for semi empirical methods II. Application, J. Comput. Chem. 10 (1989), 221-264. https://doi.org/10.1002/jcc.540100209

A. R. Leach, Molecular Modeling, Essex: Longman, 1997.

P. Fletcher, Practical Methods of Optimization, New York: Wiley, 1990.

W. Kohn and L. Sham, Self-consistent equations including exchange and correlation effects, J. Phys. Rev. 140 (1965), A1133-A1138. https://doi.org/10.1103/PhysRev.140.A1133

R.G. Parr and W. Yang, Density Functional Theory of Atoms and Molecules, London: Oxford University Press, 1989.

C.J. Cramer, Essentials of Computational Chemistry, Chichester, West Sussex: Wiley, 2004.

A.D. Becke, Density-functional exchange-energy approximation with correct asymptotic behavior, Phys. Rev. A 38 (1988), 3098-3100. https://doi.org/10.1103/PhysRevA.38.3098

S.H. Vosko, L. Wilk and M. Nusair, Accurate spin-dependent electron liquid correlation energies for local spin density calculations: a critical analysis, Can. J. Phys. 58 (1980), 1200-1211. https://doi.org/10.1139/p80-159

C. Lee, W. Yang and R.G. Parr, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density, Phys. Rev. B 37 (1988), 785-789. https://doi.org/10.1103/PhysRevB.37.785

SPARTAN 06, Wavefunction Inc., Irvine CA, USA, 2006.

A. Streitwieser, Jr., Molecular Orbital Theory for Organic Chemists, New York: Wiley, 1961.

V. Anbu, K.A. Vijayalakshmi, R. Karunathan, A.D. Stephen and P.V. Nidhin, Explosives properties of high energetic trinitrophenyl nitramide molecules: A DFT and AIM analysis, Arab. J. Chem. 12(5) (2019), 621-632. https://doi.org/10.1016/j.arabjc.2016.09.023

N.R. Badders, C. Wei, A.A. Aldeeb, W.J. Rogers and M.S. Mannan, Predicting the impact sensitivities of polynitro compounds using quantum chemical descriptors, J. Energ. Mater. 24 (2006), 17-33. https://doi.org/10.1080/07370650500374326

Published
2021-05-20
How to Cite
Türker, L. (2021). Diagonally Compressed TNAZ - A DFT Treatment. Earthline Journal of Chemical Sciences, 6(1), 65-84. https://doi.org/10.34198/ejcs.6121.6584
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