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Theoretical Studies of High-nitrogen-containing Energetic Compounds Based on the s-Tetrazine Unit

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
In order to develop new high-energy-density materials (HEDMs), we have investigated 12 substituted s-tetrazine (TZ) compounds, where s-tetrazine was substituted by amino, amido and related groups. Density functional theory (DFT) was used to predict the optimized geometries, electronic structures, total energy, heats of formation (HOFs) and densities. In addition the detonation properties were evaluated by using the VLW equation of state (EOS). The standard enthalpy of formation, the Gibbs free energy, entropy and equilibrium constants were used to estimate the success of the synthetic substitution reactions, which provided theoretical support for practical work. The bond dissociation energy (BDE) of bond C-R was calculated at each stage of the substitution reaction. The calculated results showed that substitution of amino, amido and their derivatives in the TZ ring enhances the HOF values and is favorable for increasing the thermal stability. The calculated detonation properties indicated that incorporating the above groups into the TZ ring is benefcial for improving the explosive performance. Considering the detonation properties and thermal stability, the 12 derivatives may be regarded as promising candidates as high-energy-density materials (HEDMs).
Rocznik
Strony
171--189
Opis fizyczny
Bibliogr. 22 poz., rys., tab.
Twórcy
autor
  • State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, P. R. China
autor
  • State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, P. R. China
autor
  • State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, P. R. China
autor
  • State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, P. R. China
autor
  • State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, P. R. China
Bibliografia
  • [1] Withersby M.A., Blake A.J., Champness N.R., Cooke P.A., Hubberstey P., Li W.S., Schroder M., Solvent Control in the Synthesis of 3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazine-bridged Cadmium(II) and Zinc(II) Coordination Polymers, Inorg. Chem., 1999, 38(10), 2259-2266.
  • [2] Chavez D.E., Hiskey M.A., Gilardi R.D., 3,3’-Azobis(6-amino-1,2,4,5-tetrazine): A Novel High-nitrogen Energetic Material, Angew. Chem. Int. Ed., 2000, 39(10), 1791-1795.
  • [3] Huynh M.H.V., Hiskey M.A., Chavez D.E., Naud D.L., Gilardi R.D., Synthesis, Characterization, and Energetic Properties of Diazido Heteroaromatic High-nitrogen C-N Compound, J. Am. Chem. Soc., 2005, 127(36), 12537-12543.
  • [4] Chavez D.E., Hiskey M.A., Naud D.L., Tetrazine Explosives, Propellants Explos. Pyrotech., 2004, 29(4), 209-215.
  • [5] Pagoria P.F., Lee G.S., Mitchell A.R., Schmidt R.D., A Review of Energetic Materials Synthesis, Thermochim. Acta, 2002, 384(1-2), 187-204.
  • [6] Garg S., Shreeve J.M., Trifuoromethyl- or Pentafuorosulfanyl-substituted Poly-1,2,3-triazole Compounds as Dense Stable Energetic Materials, J. Mater. Chem., 2011, 21(13), 4787-4795.
  • [7] Garau C., Quinonero D., Frontera A., Costa A., Ballester P., Deya P.M., s-Tetrazine as a New Binding Unit in Molecular Recognition of Anions, Chem. Phys. Lett., 2003, 370(1-2), 7-13.
  • [8] Wang G.X., Gong X.D., Liu Y., Du H.C., Xu X.J., Xiao, H.M., Looking for High Energy Density Compounds Applicable for Propellant among the Derivatives of DPO with –N3, -ONO2, and –NNO2 Groups, J. Comput. Chem., 2011, 32(5), 943-952.
  • [9] Ghule V.D., Sarangapani R., Jadhav P.M., Tewari S.P., Quantum-chemical Investigation of Substituted s-Tetrazine Derivatives as Energetic Materials, Bulletin of the Korean Chemical Society, 2012, 33(2), 564-570.
  • [10] Saikia A., Sivabalan R., Polke B.G., Gore G.M.,Singh A., Synthesis and Characterization of 3,6-Bis(1H-1,2,3,4-tetrazol-5-ylamino)-1,2,4,5-tetrazine (BTATz): Novel High-nitrogen Content Insensitive High Energy Material, J. Hazard. Mater., 2009, 170(1), 306-313.
  • [11] Wei T., Wu J., Zhu W., Zhang C., Xiao H., Characterization of Nitrogen-bridged 1,2,4,5-Tetrazine-, Furazan-, and 1H-Tetrazole-based Polyheterocyclic Compounds: Heats of Formation, Thermal Stability, and Detonation Properties, J. Mol. Model., 2012, 27, 1-13.
  • [12] Liang X.Q., Pu X.M., Tian A.M., Theoretial Studies on Structures and Properties of 1,2,4,5-Tetrazine Derivatives Substituted by Substituent Groups Containing Nitrogen (in Chinese), Chin. J. Organ. Chem., 2011, 3, 328-335.
  • [13] Tan B., Peng R., Long X., Li H., Jin B., Chu S., An Important Factor in Relation to Shock-induced Chemistry: Resonance Energy, J. Mol. Model., 2012, 18(2), 583-589.
  • [14] Zhou Y., Long X.P., Shu Y.J., Theoretical Studies on the Heats of Formation, Densities, and Detonation Properties of Substituted s-Tetrazine Compounds, J. Mol. Model., 2010, 16(5), 1021-1027.
  • [15] Odelius M., Kirchner B., Hutter J., s-Tetrazine in Aqueous Solution: A Density Functional Study of Hydrogen Bonding and Electronic Excitations, J. Phys. Chem., 2004, 108(11), 2044-2052.
  • [16] Kerth J., Lobbecke S., Synthesis and Characterization of 3,3’-Azobis(6-amino-1,2,4,5-tetrazine) DAAT − A New Promising Nitrogen-rich Compound, Propellants Explos. Pyrotech., 2002, 27(3), 111-118.
  • [17] Wei T., Zhu W.H., Zhang J.J., Xiao H.M., DFT Study on Energetic Tetrazolo-1,5-b -1,2,4,5-tetrazine and 1,2,4-Triazolo- 4,3-b -1,2,4,5-tetrazine Derivatives, J. Hazard. Mater., 2010, 179(1-3), 581-590.
  • [18] Adamo C., Barone V., A TD DFT Study of the Electronic Spectrum of s-Tetrazine in the Gas-phase and in Aqueous Solution, Chem. Phys. Lett., 2000, 330(1-2), 152-160.
  • [19] Wang F., Du H.C., Zhang J.Y., Gong X.D., A Theoretical Study on the Structures, Thermodynamic Properties and Detonation Performances of Azidamines, Mol. Simul., 2011, 37(10), 893-898.
  • [20] Sharma P., Kumar A., Singh J., Sahu V., Theoretical Evaluation of the Global and Local Electrophilicity Patterns to Characterize Hetero Diels-Alder Cycloaddition in the Synthesis of Isoxazolo 4,5-e (1,2,3,4-tetrazine), Chin. J. Chem., 2009, 27(5), 868-876.
  • [21] Frisch M.J., Trucks G.W., Schlegel H.B., et al. (Ed.) GAUSSIAN 03, Rew B 03., Pittsburgh, PA, 2003.
  • [22] Wu X., Long X.P., He B., Jiang X.H., VLW Equation of State on the Products of Detonation (in Chinese), Sci. China Ser. B-Chem, 2008, 38(52), 1129-1132.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-8a9be47e-a924-49d7-b1af-17717b254530
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