Thermodynamic properties, decomposition kinetics of 2-(5-amino-2H-tetrazol-1-yl)-4-amine-3,5-dinitropyridine.

A novel energetic material 2-(5-amino-2H-tetrazol-1-yl)-4-amine-3,5-dinitropyridine (ATDP) was synthesized and characterized by 1H NMR, 13C NMR, mass spectroscopy, and elemental analysis. The research by differential scanning calorimetry (DSC) shows that ATDP decomposed about 290 °C. The calculating results of kinetic parameters using Ozawa method, Kissinger method, and Starink method were quite consistent. Self-accelerated decomposition temperature (TSADT), thermal ignition temperature (TTIT), and critical temperature of thermal explosion (Tb) were 272.55 °C, 121.71 °C, and 137.67 °C, respectively. Geometric optimization, heat of formation, detonation velocity (D), detonation pressure (P), bond dissociation energy (BDE), and electrostatic potential (ESP) were explored using Gaussian 16. The results show that ATDP has a much larger ΔHf,gas value than HMX(272.6 kJ mol-1). The D and P are predicted with the value of 7.50 km s-1 and 24.47 GPa, respectively. The relatively high BDE value (270.77 kJ mol-1) indicates that ATDP has moderate thermal stability.

Theoretical Studies on the Performance of HMX with Different Energetic Groups.

Forty nitramines by incorporating -C=O, -NH2, -N3, -NF2, -NHNO2, -NHNH2, -NO2, -ONO2, -C(NO2)3, and -CH(NO2)2 groups based on a 1,3,5,7-tetranitro-1,3,5,7-tetraazacyclooctane (HMX) framework were designed. Their electronic structures, heats of formation (HOFs), detonation properties, thermal stabilities, electrostatic potential, and thermodynamic properties were systematically investigated by density functional theory. The comprehensive relationships between the structures and performance of different substituents were studied. Results indicate that -C(NO2)3 has the greatest effect on improvement of HOFs among the whole substituted groups. Thermodynamic parameters, such as standard molar heat capacity (C p,m θ), standard molar entropy (S m θ), and standard molar enthalpy (H m θ), of all designed compounds increase with the increasing number of energetic groups, and the volumes of energetic groups have a great influence on standard molar enthalpy. Except for -NH2(R1), -NHNH2(R5), and B3, all of the designed compounds have higher detonation velocities and pressures than HMX. Among them, E7 exhibits an extraordinarily high detonation performance (D = 10.89 km s-1, P = 57.3 GPa), E1 exhibits a relatively poor detonation performance (D = 8.93 km s-1, P = 35.5 GPa), and -NF2 and -C(NO2)3 are the best ones in increasing the density by more or less 12%.

Theoretical Study on CL-20-Based Cocrystal Energetic Compounds in an External Electric Field.

An external electric field has great effects on the sensitivity of cocrystal energetic materials. In order to find out the relationship between the external electric field and sensitivity of cocrystals 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane/benzotrifuroxan (CL-20/BTF), 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane/3,4-dinitropyrazole (CL-20/DNP), and 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane/1-methyl-3,5-dinitro-1,2,4-triazole (CL-20/MDNT), density functional theory at B3LYP-D3/6-311+G(d,p) and M062X-D3/ma-def2 TZVPP levels was employed to calculate frontier molecular orbitals, atoms in molecules (AIM) electron density values, bond dissociation energies (BDEs) of the N-NO2 bond, impact sensitivity (H 50), electrostatic potentials (ESPs), and nitro group charges (Q NO2 ) in this work. The results show that a smaller highest occupied molecular orbital-lowest unoccupied molecular orbital gap and the BDEs, as well as H 50, tend to have a larger sensitivity along with the positive directions in the external electric field. Moreover, a smaller local positive ESP (V s max) leads to better stability in the negative electric field. The sensitivity of cocrystal molecules decreases gradually in the negative external electric field with the increase of negative nitro group charges. Finally, the change in the bond lengths, AIM electron density values, and nitro group charges correlate well with the external electric field strengths.

Pressure induced structural behavior of energetic cocrystal TNT/TNB: a density functional theory study.

In order to find out the relationship between external pressures and properties of energetic materials, we used the density functional theory (DFT) method to investigate the structural, electronic, and absorption properties of crystalline 2,4,6-trinitrotoluene (TNT)/2,4,6-trinitrotoluene (TNB) under hydrostatic compression of 0-100 GPa. By analyzing the change of lattice constants (a, b, and c) of TNT/TNB under compression conditions, we found that variation tendency of the lattice constants was anisotropic. The b-axis is much stiffer than that along the a- and c-axes, which indicates that the TNT/TNB crystal is anisotropic within a certain pressure region. The pressure-induced structure transformation results in the new covalent bonds O11-C13, O12-C11, O8-C4, and O1-C12 at 60 GPa, and O4-C5 at 80 GPa, respectively. By analyzing the band structure and density of states of TNT/TNB in the pressure range over 40 GPa, the electronic structure of TNT/TNB changed to metallic system, which indicated it becomes more sensitivity under high pressures. The pressure-induced structure transformation of TNT/TNB also contributed to the relatively high optical activity of TNT/TNB at 70 GPa.

Molecular design and properties of bridged energetic pyridines derivatives.

A series of bridged pyridine-based energetic derivatives were designed and their geometrical structures, electronic structures, heats of formation, detonation properties, thermal stabilities, thermodynamic properties and electrostatic potential were fully investigated using density functional theory. The results show that the steric hindrance effect is a decisive factor for structural stability, and the formation of intramolecular or intermolecular hydrogen bonds doesn't provide advantages to stabilize molecular structure, which was demonstrated by insertion of 3,4,5-trinitro-1H-pyrazole, 3,4-dinitro-1H-pyrazol-5-amine, 3,5-dinitro-1H-pyrazol-4-amine and 3-nitro-1H-1,2,4-triazol-5-amine. The azide group and azo bridge play an important role in improving the heats of formation of energetic pyridine-based materials. All designed molecules were found to have values of density ranging from 1.70 g cm-3 (E6, F6) to 2.11 g cm-3 (D3), values of detonation velocity ranging from 7.1 km s-1 (F1) to 9.77 km s-1 (D8), and values of detonation pressure ranging from 21.5 GPa (F1) to 46.0 GPa (D8). When a p-π conjugation formed between the nitrogen atom and pyridine ring, the bond between nitrogen and hydrogen atoms may be broken as the trigger bond.