Taming of Triazole, Tetrazole, and Azido Groups: Nitrogen-Rich Energetic Materials with High Thermal Stabilities.

Nitrogen-rich energetic materials are of interest due to their potential use as high-energy-density materials in various applications. However, most compounds with a high nitrogen content show poor thermal stabilities, which may limit their use in certain applications. In pursuit of nitrogen-rich energetic materials, this study presents the synthesis and characterization of two nitrogen rich energetic compounds, namely 3-azido-1-(1H-tetrazol-5-yl)-1H-1,2,4-triazol-5-amine (3, C3H3N11, N%: 79.78) and (E)-1,2-bis(3-azido-1-(1H-tetrazol-5-yl)-1H-1,2,4-triazol-5-yl) diazene (7, C6H2N22, N%: 80.62). Compounds 3 and 7 have high thermal stabilities of 216 and 221 °C, respectively, making them the most thermally stable among metal-free primary explosives. Additionally, they show good energetic performance (vD: 8345 m s-1; P: 25.17 GPa; vD: 8275 m s-1; P: 25.57 GPa), making them potential candidates for metal-free high energy primary explosive. The energetic salts of 3 and 7 were also investigated. Among them, hydrazinium salt 11 displays better energetic performance (vD: 9089 m s-1; P: 30.55 GPa), which was on par with those of cyclotetramethylene tetranitramine (HMX). This research contributes to the exploration of nitrogen-rich energetic materials with potential applications in various fields.

First Alliance of Pyrazole and Furoxan Leading to High-Performance Energetic Materials.

Nitrogen heterocyclic scaffolds retain their leading position as valuable building blocks in material science, particularly for the design of small-molecule energetic materials. However, the search for more balanced combinations of directly linked heterocyclic cores is far from being exhausted and aims to reach ideally balanced high-energy substances. Herein, we present the synthetic route to novel pyrazole-furoxan framework enriched with nitro groups and demonstrate a promising set of properties, viz., good thermal stability, acceptable mechanical sensitivity, and high detonation performance. In-depth crystal analysis showed that the isomers having lower-impact sensitivity values in both types of regioisomeric pairs are those with the exocyclic furoxan oxygen atom being closer to the pyrazole ring. Owing to the favorable combination of high crystal densities (1.83-1.93 g cm-3), positive oxygen balance to CO (up to +13.9%), and high enthalpies of formation (322-435 kJ mol-1), the synthesized compounds show high calculated detonation velocities (8.4-9.1 km s-1) and excellent metal accelerating abilities. The incorporation of the 3-nitrofuroxan moiety increases the thermal stability (by ca. 20 °C) and decreases the mechanical sensitivity of target hybrid materials in both types of regioisomeric pairs. Simultaneously, the detonation performance of 3-nitrofuroxans is almost identical to that of 4-nitrofuroxans, highlighting the potential of the regioisomeric tunability in the future design of energetic materials.

Theoretical study on multi-perspective interaction analysis of ADN and ADN-H2O-CH3OH solutions.

CONTEXT: Revealing the mechanism of intermolecular interactions in dinitroamine ammonium (ADN)-based liquid propellants and exploring the reasons for their performance changes, multi-perspective interaction analyses of ADN and ADN-water (H2O)-methanol (CH3OH) solutions have been conducted via theoretical methods. The band structure, density of states (DOS), surface electrostatic potential (ESP), Hirshfeld surface, reduced density gradient (RDG), AIM topological analysis, and detonation performance were studied and the results showed that both the ADN and ADN-H2O-CH3OH solutions had hydrogen bonds and van der Waals interactions. By introducing the small molecules H2O and CH3OH, the detonation performance of the ADN-H2O-CH3OH solution slightly decreased, but its sensitivity also decreased. Overall, the comprehensive performance of the ADN-H2O-CH3OH solution has improved, and the application range has expanded. These results are helpful for obtaining a deeper understanding of ADN-based liquid propellants at the atomic level and contribute to the development of new liquid propellants. METHODS: The ADN and ADN-H2O-CH3OH solutions were constructed by Amorphous cell module and optimized via GGA with PBE methods in the Dmol3 module of the Materials Studio, and their electronic properties were calculated. Hirshfeld surfaces were generated with CrystalExplorer 3.0. A topological analysis of a variety of molecular clusters was performed via QTAIM. The QTAIM and RDG analyses in this work were generated by Multiwfn 3.0.

Trinitromethyl-Substituted 1H-1,2,4-Triazole Bridging Nitropyrazole: A Strategy of Utterly Manipulable Nitration Achieving High-Energy Density Material.

Nitro groups have been demonstrated to play a decisive role in the development of the most powerful known energetic materials. Two trinitromethyl-substituted 1H-1,2,4-triazole bridging nitropyrazoles were first synthesized by straightforward routes and were characterized by chemical (MS, NMR, IR spectroscopy, and single-crystal X-ray diffraction) and experimental analysis (sensitivity toward friction, impact, and differential scanning calorimetry-thermogravimetric analysis test). Their detonation properties (detonation pressure, detonation velocity, etc.) were predicted by the EXPLO5 package based on the crystal density and calculated heat of formation with Gaussian 09. These new trinitromethyl triazoles were found to show suitable sensitivities, high density, and highly positive heat of formation. The combination of exceedingly high performances superior to those of HMX (1,3,5,7-tetranitrotetraazacyclooctane), and its straightforward preparation highlights compound 8 as a promising high-energy density material (HEDM). This work supports the effectivity of utterly manipulable nitration and provides a generalizable design synthesis strategy for developing new HEDMs.

Enhancing Conjugation Effect to Develop Nitrogen-Rich Energetic Materials with Higher Energy and Stability.

This work reports a strategy by enhancing conjugation effect and synthesizes a symmetrical and planar compound, 1,2-bis (4,5-di(1H-tetrazol-5-yl)-2H-1,2,3-triazol-2-yl)diazene (NL24). The incorporation of azo and 1,2,3-triazole moieties manifests a synergistic effect, amplifying the conjugation effect of the azo bridge and thereby elevating the stability of NL24 (Td: 263 °C, IS: 7 J). Notably, NL24, possessing a structural configuration comprising four tetrazoles harboring a total of 24 nitrogen atoms, exhibits excellent detonation performances (ΔHf: 6.06 kJ g-1, VD: 9002 m s-1). This strategy achieves the balance of energy and stability of polycyclic tetrazoles and provides a direction for high-performance energetic materials.

Polyvalent Ionic Energetic Salts Based on 4-Amino-3-hydrazino-5-methyl-1,2,4-triazole.

The synthesis of the new energetic material 4-amino-3-hydrazino-5-methyl-1,2,4-triazole, which shows excellent performance and reliable safety, has drawn attention recently. To fully characterize this material, a comprehensive analysis was performed using various techniques, including differential scanning calorimetry (DSC), infrared spectroscopy (IR), elemental analysis, and 1H and 13C NMR spectroscopy. Additionally, three compounds, 3, 5 and 9, were further characterized using single X-ray diffraction. The X-ray data suggested that extensive hydrogen bonds affect molecular structure by means of intermolecular interactions. In order to evaluate the explosive properties of these synthesized compounds, detonation pressures and velocities were calculated using EXPLO5 (V6.01). These calculations were carried out utilizing experimental data, including density and heat of formation. Among the explosives tested, compounds 7 and 8 exhibited zero oxygen balance and demonstrated exceptional detonation properties. Compound 7 achieved the highest recorded detonation pressure, at 34.2 GPa, while compound 8 displayed the highest detonation velocity, at 8887 m s-1.

Design and Synthesis of Energetic Melt-Castable Materials by Substituent-Specific Modification.

With the increase in the demand for high-performance composite explosives, the search for advanced energetic melt-castable compounds has attracted increasing attention in the field of energetic materials. Herein, two new energetic materials with nitromethyl and azidomethyl substituents (1-(nitromethyl)-3,4-dinitro-1H-pyrazole (NMDNP) and 1-(azidomethyl)-3,4-dinitro-1H-pyrazole (AMDNP) were prepared by the substituent modification of a potential melt-castable molecule ((3,4-dinitro-1H-pyrazol-1-yl) methyl nitrate, MC-4), respectively. NMDNP exhibited a suitable melting point (90 °C), good thermal stability (Td : 185 °C) and excellent detonation performance (8484 m s-1 ) and impact sensitivity (25 J), thereby demonstrating promise as an energetic melt-castable material. Simultaneously, compared with the nitrato-methyl and azidomethyl substituents, the nitromethyl substituent exhibited greater advantages in regulating performance.

2,2'-Azobis(1,5'-bitetrazole) with a N10 Chain and 1,5'-Bitetrazolate-2N-oxides: Construction of Highly Energetic Nitrogen-Rich Materials Based on C-N-Linked Tetrazoles.

A series of high-nitrogen compounds, including a unique molecule 2,2'-azobis(1,5'-bitetrazole) with a branched N10 chain and 1,5'-bitetrazolate-2N-oxides, were synthesized successfully based on C-N-linked 1,5'-bistetrazoles using azo coupling of N-amine bonds and N-oxide introduction strategies. All compounds were characterized by NMR spectroscopy, IR spectroscopy, elemental analysis, and differential scanning calorimetry, in which the structures of five compounds were further determined by single-crystal X-ray diffraction analysis (2, T-N10B, 3a, 3b, and THX). The nitrogen contents of these five compounds range from 63.62 (THX) to 83.43% (T-N10B), which are much higher than that of CL-20 (38.34%). The heat of formation for the prepared compounds was calculated by using the Gaussian 09 program, with T-N10B having the highest value of 5.13 kJ g-1, about 6 times higher than that of CL-20 (0.83 kJ g-1). The calculated detonation performances by EXPLO5 v6.05.04 show that THX has excellent detonation performance (D = 9581 m s-1, P = 35.93 GPa) and a remarkable specific impulse (Isp = 284.9 s).

Periodate-Based Perovskite Energetic Materials: A Strategy for High-Energy Primary Explosives.

The requirements for high energy and green primary explosives are more and more stringent because of the rising demand in the application of micro initiation explosive devices. Four new energetic compounds with powerful initiation ability are reported and their performances are experimentally proven as designed, including non-perovskites ([H2 DABCO](H4 IO6 )2 ·2H2 O, named TDPI-0) and perovskitoid energetic materials (PEMs) ([H2 DABCO][M(IO4 )3 ]; DABCO=1,4-Diazabicyclo[2.2.2]octane, M=Na+ , K+ , and NH4 + for TDPI-1, -2, and -4, respectively). The tolerance factor is first introduced to guide the design of perovskitoid energetic materials (PEMs). In conjunction with [H2 DABCO](ClO4 )2 ·H2 O (DAP-0) and [H2 DABCO][M(ClO4 )3 ] (M=Na+ , K+ , and NH4 + for DAP-1, -2, and -4), the physiochemical properties of the two series are investigated between PEMs and non-perovskites (TDPI-0 and DAP-0). The experimental results show that PEMs have great advantages in improving the thermal stability, detonation performance, initiation capability, and regulating sensitivity. The influence of X-site replacement is illustrated by hard-soft-acid-base (HSAB) theory. Especially, TDPIs possess much stronger initiation capability than DAPs, which indicates that periodate salts are in favor of deflagration-to-detonation transition. Therefore, PEMs provide a simple and feasible method for designing advanced high energy materials with adjustable properties.

Theoretical study on the structure, electronic properties, intermolecular interactions, and detonation performance of DAF:ADNP co-crystal.

CONTEXT: Explosives have a wide range of applications in many fields due to their high energy and high density. Recently, a new synthesized co-crystal explosive DAF:ADNP presents high detonation performance and low sensitivity. This work is aimed to understand how the structure and intermolecular interactions affect the performance of the DAF:ADNP co-crystal. The results indicate that the formed π-π interactions and stronger hydrogen bonds in the co-crystal enhance its stability and its impact sensitivity is reduced. The strong intralayer H···N and H···O interactions and interlayer π-π stacking are the main driving force for the formation of the co-crystal. Compared with the pure crystals, the detonation performance of the co-crystal slightly decreases, while its sensitivity reduces. METHODS: All calculations were used the DFT-PBE-D method with Vanderbilt-type ultrasoft pseudopotentials and plane wave (340.0 eV) in the CASTEP package. Radial distribution function were calculated by NVT-MD simulations for 100 ps with a time step of 1 fs at 298 K. Hirshfeld surfaces were generated by CrystalExplorer 3.0 and reduced density gradient analyses were performed by Multiwfn 3.0.

Insensitive High-Energy Density Materials Based on Azazole-Rich Rings: 1,2,4-Triazole N-Oxide Derivatives Containing Isomerized Nitro and Amino Groups.

It is an arduous and meaningful challenge to design and develop new energetic materials with lower sensitivity and higher energy. How to skillfully combine the characteristics of low sensitivity and high energy is the key problem in designing new insensitive high-energy materials. Taking a triazole ring as a framework, a strategy of N-oxide derivatives containing isomerized nitro and amino groups was proposed to answer this question. Based on this strategy, some 1,2,4-triazole N-oxide derivatives (NATNOs) were designed and explored. The electronic structure calculation showed that the stable existence of these triazole derivatives was due to the intramolecular hydrogen bond and other interactions. The impact sensitivity and the dissociation enthalpy of trigger bonds directly indicated that some compounds could exist stably. The crystal densities of all NATNOs were larger than 1.80 g/cm3, which met the requirement of high-energetic materials for crystal density. Some NATNOs (9748 m/s for NATNO, 9841 m/s for NATNO-1, 9818 m/s for NATNO-2, 9906 m/s for NATNO-3, and 9592 m/s for NATNO-4) were potential high detonation velocity energy materials. These study results not only indicate that the NATNOs have relatively stable properties and excellent detonation properties but also prove that the strategy of nitro amino position isomerization coupled with N-oxide is an effective means to develop new energetic materials.

Trinitromethyl Energetic Groups Enhance High Heats of Detonation.

The introduction of groups with high enthalpies of formation can effectively improve the detonation performance of the compounds. A series of novel energetic compounds (10-13) with high enthalpies of formation, high density, and high nitrogen-oxygen content were designed and synthesized by combining gem-polynitromethyl, 1,2,4-oxadiazole, furoxan, and azo groups. All the new compounds were thoroughly characterized by IR, NMR, elemental analysis, and differential scanning calorimetry. Compounds 10 and 11 were also further characterized with single-crystal X-ray diffraction. Compound 11 has high density (1.93 g cm-3), high enthalpy of formation (993.5 kJ mol-1), high detonation velocity (9411 m s-1), and high heat of detonation (6889 kJ kg-1) and is a potentially excellent secondary explosive.

The ionic salts with super oxidizing ions O2 + and N5 +: Potential candidates for high-energy oxidants.

As an important component of energetic materials, high-energy oxidant is one of the key materials to improve their energy. The oxidizability of oxidant directly determines the intensity of combustion or explosion reaction. It is generally believed that when the nature of reductant is certain, the stronger the oxidizability, the more intense the reaction. Dioxygenyl cation (O2 +) and pentazenium cation (N5 +) are two kinds of super oxidizing ions, which oxidizability are comparable to that of fluorine. A series of high energetic ionic salts with O2 +, N5 + and various anions as active components are designed, and the results show that: 1) Most ionic salts have appropriate thermodynamic stability, high density (up to 2.201 g/cm3), high enthalpy of formation (up to 1863.234 kJ/mol) and excellent detonation properties (up to 10.83 km/s, 45.9 GPa); 2) The detonation velocity value of O2 (nitrotetrazole-N-oxides) and O2B(N3)4 exceed 10.0 km/s, and the detonation pressure exceed 45.0 GPa because of the O2 + salts have higher crystal density (g/cm3) and oxygen balance than that of N5 +salts; 3) With a higher nitrogen content than O2 +, the N5 + salts have higher enthalpy of formation, which exceed 330 kJ/mol than that of O2 + salts; 4) The linear spatial structure of N5 + leads the salts to reduce their density. Encouragingly, this study proves that these super oxidizing ions have the potential to become high-energy oxidants, which could be a theoretical reference for the design of new high energetic materials.

Boosting the Energetic Performance of Trinitromethyl-1,2,4-oxadiazole Moiety by Increasing Nitrogen-Oxygen in the Bridge.

The trinitromethyl moiety is a useful group for the design and development of novel energetic compounds with high nitrogen and oxygen content. In this work, by using an improved nitration method, the dinitromethyl precursor was successfully nitrated to the trinitromethyl product (2), and its structure was thoroughly characterized by FTIR, NMR, elemental analysis, differential scanning calorimetry, and single-crystal X-ray diffraction. Compound 2 has a high density (1.897 g cm-3), high heat of formation (984.8 kJ mmol-1), and a high detonation performance (D: 9351 m s-1, P: 37.46 GPa) that may find useful applications in the field of high energy density materials.

Recent Progress on Synthesis, Characterization, and Performance of Energetic Cocrystals: A Review.

In the niche area of energetic materials, a balance between energy and safety is extremely important. To address this "energy-safety contradiction", energetic cocrystals have been introduced. The investigation of the synthesis methods, characteristics, and efficacy of energetic cocrystals is of the utmost importance for optimizing their design and development. This review covers (i) various synthesis methods for energetic cocrystals; (ii) discusses their characteristics such as structural properties, detonation performance, sensitivity analysis, thermal properties, and morphology mapping, along with other properties such as oxygen balance, solubility, and fluorescence; and (iii) performance with respect to energy contents (detonation velocity and pressure) and sensitivity. This is followed by concluding remarks together with future perspectives.

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.

Chemical study of fused ring tetrazine derivatives as possible high energy density materials (HEDMs).

Using density functional theory (DFT), enthalpy of formation (HOF), thermodynamic properties, and detonation properties of a series of tetrazine fused ring derivatives are calculated. The results show that the introduction of coordinated oxygen is beneficial to increase the HOF value. The effects of different substituents on HOF are as follows: -C(NO2)3 > -N3 > -CH(NO2)2 > -NHNO2 > -NO2 > -NHNH2 > -H > -OH. Introduction of -H, -NH2, and -NHNH2 on the parent is not conducive to improving the detonation performance, while the introduction of -C(NO2)3 is conducive to improving the detonation performance of the designed compound. The explosion velocity of the newly designed compounds varies between 8.96 and 10.48 km·s-1. The explosion pressure varies between 35.97 and 51.80 GPa, and the density varies between 1.83 and 2.00 g·cm-3. Considering the thermal stability, density, and detonation properties, most of these compounds designed this time can be used as potential candidates for high energy density compounds.

What Shall We Do with the Computed Detonation Performance? Comment on "1,3,4-Oxadiazole Bridges: A Strategy to Improve Energetics at the Molecular Level".

In this Correspondence, a question is raised on how confident are the computed detonation performance values. Consideration of the energetic materials in a recent Research Article in this journal and some other newly synthesized promising compounds shows that the variation between the available methods of calculation is surprisingly high.

Response to "What Shall We Do with Computed Detonation Performance? Comment on '1,3,4-Oxadiazole Bridges: A Strategy to Improve Energetics at the Molecular Level'".

The values obtained for detonation performance are a function of the computational methods utilized. Since there are many such methods, the literature may contain a range of values for a single compound.

Theoretical study of effects of introducing varying linkages into bis-triazoles on energetic performance.

A series of novel bis-triazole compounds was designed by combining high-energy functionalities (nitro and nitramino groups) as substituents with each triazole and incorporating of varying linkages into the bis-triazoles. Then, their heats of formation (HOFs), energetic properties, HOMO-LUMO, electrostatic potential, and impact sensitivity were studied theoretically to facilitate further developments. In general, all the designed compounds possess much higher HOFs than RDX, -CH2-CH2-, -N=N-, or -NH-NH- linkages contribute to increase the HOFs, while incorporation of the bridge group -O-CH2-CH2-O- shows negative effect on HOFs. Detonation properties of most of the designed compounds can be comparable with or even better than ones of RDX, suggesting that designing the bridged bis-triazoles-based derivatives with energy-rich substituents is an efficient method to obtain potential energetic compounds. Considering the detonation performance and impact sensitivity, -NH-(I), -N=N- (V), and -NH-NH- (VI) are favorable bridged groups between energetic moieties for designing efficient energetic materials (EMs).