The β‐δ‐Phase Transition and Thermal Expansion of Octahydro‐1,3,5,7‐Tetranitro‐1,3,5,7‐Tetrazocine

Phase behavior of octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine (HMX) is investigated by X‐ray powder diffraction (XRD). The XRD patterns at elevated temperature show that there is a co‐existing temperature range of β‐ and δ‐phase during the phase transition process. Additionally, mechanical forces can catalyze the conversion from δ‐ back to β‐phase. Based on the diffraction patterns of β‐ and δ‐phase at different temperatures, we calculate the coefficients of thermal expansion by Rietveld refinement. For β‐HMX, the linear coefficients of thermal expansion of a‐axis and b‐axis are about 1.37×10⁻⁵ and 1.25×10⁻⁴ °C⁻¹. A slight decrease in c‐axis with temperature is also observed, and the value is about −0.63×10⁻⁵ °C⁻¹. The volume coefficient of thermal expansion is about 1.60×10⁻⁴ °C⁻¹, with a 2.2% change from 30 to 170 °C. For δ‐HMX, the linear coefficients of thermal expansion of a‐axis and c‐axis are found to be 5.39×10⁻⁵ and 2.38×10⁻⁵ °C⁻¹, respectively. The volume coefficient of thermal expansion is about 1.33×10⁻⁴ °C⁻¹, with a 2.6% change from 30 to 230 °C. The results indicate that β‐HMX has a similar volume coefficient of thermal expansion compared with δ‐HMX, and there is about 10.5% expansion from β‐HMX at 30 °C to δ‐HMX at 230 °C, of which about 7% may be attributed to the reconstructive transition.     

Analysis of Polar Precursors of 1,3,5,7‐Tetranitro‐1,3,5,7‐tetrazocine (HMX) Using Hydrophilic Interaction Chromatography

Octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine (HMX) is currently one of the most widely used explosives. 1,3,5,7‐Tetraacetyl‐1,3,5,7‐tetraazacyclooctane (TAT) is an attractive precursor for the synthesis of HMX; the nitration of this key precursor results in both high yield and purity under mild condition. TAT can be prepared either by acetylation of 2,6‐diacetyl‐pentamethylenetetramine (DAPT) or by the condensation of ACN and 1,3,5‐trioxane. However, TAT and DAPT are polar compounds, and are difficult to analyze using reverse phase liquid chromatography. Herein, a chromatography method for the direct separation of these polar compounds was developed using hydrophilic interaction chromatography (HILIC) using a Venusil HILIC column, with ACN/water (95/5, v/v) as the mobile phase. The chromatographic analysis and identification of these polar compounds provide valuable information for the optimization of the synthetic process of TAT.     

Selective Extraction of N‐Heterocyclic Precursors of 1,3,5,7‐Tetranitro‐1,3,5,7‐tetraazacyclooctane (HMX) Using Molecularly Imprinted Polymers

N‐heterocyclic compounds are key nitration precursors for some high energy density explosives such as 1,3,5,7‐tetranitro‐1,3,5,7‐tetraazacyclooctane (HMX). Nitration of 1,3,5,7‐tetraacetyl‐1,3,5,7‐tetraazacyclooctane (TAT) yields HMX in high yields and purity. However, the analogue 1,3,5‐triacetyl‐1,3,5‐triazacyclohexane (TRAT) is easily co‐produced via the condensation of acetonitrile and 1,3,5‐trioxan. To selectively extract TAT from a mixture of TAT and TRAT, the molecular imprinting technology (MIT) was developed in this study. The capacity of the dry polymer is 16 mg g⁻¹ and the recovery surpasses 75 %.     

Chemical Transformation of Octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine (HMX) Induced by Low Energy Electron Beam Irradiation

The effects of 8.0×10⁻¹⁷ J (500 eV) and 3.2×10⁻¹⁹ J (2 eV) electrons on chemical structure of octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine (HMX) were studied in situ, under ultra‐high vacuum conditions using a combination of X‐ray photoelectron spectroscopy (XPS) and quadrupole mass spectrometry. XPS data indicated that electrons impact by 8.0×10⁻¹⁷ J for 30 s caused a decrease in nitro group concentration, and a little shift in the binding energy of the nitrogen 1s peak. Such a phenomenon was found at very low kinetic energy (3.2×10⁻¹⁹ J) with time evolution. Quadrupole mass spectrometry detected gas desorption after electron irradiation included H₂O and H₂ mostly. Microscopy‐IR spectroscopic investigations also proved that the intensity of nitro groups of HMX after irradiation decreased compared with those of the pristine HMX. We attributed the structure changes obtained by XPS and IR spectroscopy result in a chemical transformation, which was associated with low‐energy dissociative electron attachment (DEA) of surface contaminants followed by deoxidization reactions to form the product molecules.     

Dependence of the Mechanical Sensitivity on the Fractal Characteristics of Octahydro‐1,3,5,7‐tetranitro‐1,3,5,7‐tetrazocine Particles

Three fabrication methods were used to synthesize HMX powders with different particle sizes and microscopic morphologies. All as‐prepared samples were characterized by laser granularity measurements and scanning electron microscopy (SEM). The mechanical sensitivity and thermal stability of the different HMX powders were characterized using mechanical sensitivity tests and differential scanning calorimetry (DSC). Size distribution data and SEM images were used to find the size fractal dimension (D) and surface fractal dimension (D_s) of HMX samples, which were calculated by the least‐squares method and fractal image processing software (FIPS), respectively. The parameters D and D_s quantize two important properties of HMX particles, namely the complexity of the particle size distribution and the irregularity of the particle surface, which affect the thermal conductivity of the particle group if it is exposed to stimuli such as impact, friction or heating. The fractal dimensions reveal the dependence of the mechanical sensitivity of HMX on the powder size, size distribution and microscopic morphology. The results indicate that the proportion of fine particles in HMX powder increases as the D value increases, which causes decreased impact sensitivity. This occurs because hot spot formation leading to an explosion is more difficult because of the improved thermal conductivity of the particle group. Similarly, the surface roughness of HMX particles increases with an increase in D_s, causing an increase in friction sensitivity because of the excessive accumulation of frictional heat. In addition, thermal analysis results indicate that the maximum thermal decomposition rate of HMX decreases with increasing D and D_s.     

Thermal Behavior and Thermolysis Kinetics of the Explosive Trans‐1,4,5,8‐Tetranitro‐1,4,5,8‐Tetraazadecalin (TNAD)

Trans‐1,4,5,8‐Tetranitro‐1,4,5,8‐Tetraazadecalin (TNAD), a cyclic nitroamine, has been studied with regard to the kinetics and mechanism of thermal decomposition, using thermogravimetry (TG), IR spectroscopy, and pressure differential scanning calorimetry (PDSC). The IR spectra of TNAD have also been recorded, and the kinetics of thermolysis has been followed by non‐isothermal TG. The activation energy of the solid‐state process was determined by using the Flynn‐Wall‐Ozawa method. Compared with the activation energy obtained from the Ozawa method, the reaction mechanism of the exothermic process of TNAD was classified by the Coats‐Redfern method as a nucleation and nuclear growth (Avrami equation 1) chemical reaction (α=0.30–0.60) and a 2D diffusion (Valensi equation) chemical reaction (α=0.60–0.90). E_a and ln A were established to be 330.14 kJ mol⁻¹ and 29.93 (α=0.30–0.60) or 250.30 kJ mol⁻¹ and 21.62 (α=0.60–0.90).     

Theoretical Studies on Molecular and Explosive Properties of 4,4′,5,5′‐Tetranitro‐2,2′‐bi‐1H‐imidazole (TNBI)

We performed theoretical studies to predict the molecular structure, molecular properties, and explosive performance of 4,4′,5,5′‐tetranitro‐2,2′‐bi‐1H‐imidazole (TNBI). High levels of ab initio and density functional theories were employed to predict the molecular structure of TNBI. Predicted TNBI structure was in good agreement with that observed by X‐ray crystallography. Heat of formation in the solid phase at 298 K was predicted to be 270.3 kJ/mol. Density of TNBI was predicted to be 1.919–1.956 g/cm³ depending upon the parameter sets of group additivity method. By using these values as input data, we estimated detonation velocity and C–J pressure to be 8.69–8.80 km/s and 34.5‐36.1 GPa, respectively. Impact sensitivity of TNBI was predicted to be 33 cm.     

Synthesis and Characterization of 4,4′,5,5′‐Tetranitro‐2,2′‐Bi‐1H‐imidazole (TNBI)

We synthesized 4,4′,5,5′‐tetranitro‐2,2′‐bi‐1H‐imidazole (TNBI), which may serve as a new energetic filler for high explosive formulations. TNBI was synthesized by treating an excess amount of sodium nitrate with 2,2′‐bi‐1H‐imidazole (BI), which was produced from glyoxal and ammonia gas. The overall synthetic yield was 32%. The synthesized TNBI was characterized by performing various chemical analyses including NMR, IR, and CHN analyses. Small scale sensitivity tests were carried out at both research institutes (ADD and ARDEC). The sensitivity results varied from ‘more sensitive than RDX’ to ‘substantially less sensitive than RDX’ according to the purity and conditions of the test samples. Based on our careful characterizations, this large variation in sensitivity was attributed to the moisture content that was present in the test samples due to a hygroscopic nature of TNBI. We also found that the hygroscopic nature of TNBI changed significantly due to the amount of impurities, especially sulfates.     

Synthesis and Energetic Properties of 4,4′,5,5′‐Tetranitro‐2,2′‐biimidazolate(N4BIM) Salts

This paper describes the synthesis and characterization of several salts of 4,4′,5,5′‐tetranitro‐2,2′‐biimidazolate (N4BIM). Each of the salts were characterized chemically, thermally, morphologically, as well as with respect to destructive stimuli (impact, electrostatic discharge, friction, thermal). These salts show promise as propellant ingredient additives, and in particular, the bis‐triaminoguanidinium salt of N4BIM displays excellent burn rate and combustion behavior. Our combustion studies have shown that TAGN4BIM displays a fast burning rate and has the lowest pressure dependence exponent yet measured for a triaminoguanidinium salt.     

Experimental and Theoretical Study of 1,5‐Diamino‐4‐H‐1,2,3,4‐Tetrazolium Perchlorate

The synthesis and characterization of 1,5‐diamino‐1,2,3,4‐tetrazolium perchlorate were carried out. Experimental evidence strongly supports the protonation of a nitrogen atom of the tetrazole ring, including the structure observed in a single crystal X‐ray diffraction study of the title compound. Quantum chemical calculations were performed at the CCSD(T)/6‐311G(2df, p)//MP2/6‐311G(d, p) level of theory to determine the relative energies of all possible N‐protonated structures of the 1,5‐diamino‐1,2,3,4‐tetrazole ring. The predicted geometry of the most stable isomer compares favorably with the experimentally observed structure.     

Bishydrazinium and Diammonium Salts of 4,4′,5,5′‐Tetranitro‐2,2′‐biimidazolate (TNBI): Synthesis and Properties

The diammonium ( 1 ) and bishydrazinium ( 2 ) salts of 4,4′,5,5′‐tetranitro‐2,2′‐biimidazolate (TNBI) were synthesized and their physical properties as well as predicted explosive performance characteristics are described. These dianionic salts are easily formed in good yields by reaction of TNBI with aqueous solutions of the cationic species. TNBI is synthesized from 2,2′‐biimidazole, which is ultimately synthesized by the condensation of aqueous glyoxal with ammonium acetate. The compounds were characterized by NMR spectroscopy, vibrational (FT‐IR and Raman) spectroscopy, elemental analysis, thermal analysis (DSC, VTS and calorimetry), and small scale safety testing (impact, friction, ESD). The measured densities and heats of formation are reported. The materials show promise for use in IM explosive and propellant formulations due to the combination of their calculated performances, thermal stability and insensitivity to stimuli.     

Gold(I)‐Catalyzed Carboaminations of Allenes by N‐Allyltetrahydro‐β‐carbolines: An Experimental and Theoretical Study

N‐Allyltetrahydro‐β‐carbolines bearing a pendant allene undergo unprecedented gold(I)‐catalyzed cyclizations proceeding with an allyl migration from the nitrogen to the allene moiety. The initial product of the gold‐catalyzed cyclization evolves either via isomerization or Cope rearrangement, leading to different scaffolds. Density function theory (DFT) calculations established that the allyl migration occurs in an asynchronous suprafacial manner.

     

Synthesis,Characterization and Thermal Behaviour of 2,4,6,8‐Tetranitro‐2,4,6,8‐Tetraazabicyclo[3.3.1]Nonane‐3,7‐Dione (TNPDU) and one of its Methylene Analogues

2,4,6,8 ‐ Tetranitro – 2,4,6,8 ‐ tetraazabicyclo[3.3.1]nonane‐3,7‐dione (TNPDU) has been synthesized from propane diurea by nitration with nitric acid‐acetic anhydride with a yield of 85 %. The molecular structure of the compound has been determined by elemental analysis, IR and ¹H‐NMR spectroscopy. Some of the properties including thermal and explosion delay behaviour of the compound and its mixtures with high explosives, are reported. An analogous compound 2,5,7,9‐tetranitro‐2,5,7,9‐tetraazabicyclo[4.3.0]nonane–8–one (TNABN) has also been evaluated for some of the explosive properties considering its good stability and insensitiveness as compared to other nitrodiurea derivatives.     

Combustion Properties of Amino‐Substituted Guanidinium 4,4′,5,5′‐Tetranitro‐2,2′‐biimidazolate(N4BIM) Salts

This paper describes the combustion properties of the amino‐substituted guanidinium 4,4′,5,5′‐tetranitro‐2,2′‐biimidazolate (N4BIM) series, including the bis‐mono, di and triaminoguanidinium salts. These salts are of interest as propellant ingredient additives, and in particular, the bis‐triaminoguanidinium salt of N4BIM displays excellent burn rate and combustion behavior. Our combustion studies have shown that TAGN4‐BIM displays a fast burning rate and has the lowest pressure dependence exponent yet measured for a triaminoguanidinium salt.     

Photophysics of Structurally Modified Flavin Derivatives in the Blue‐Light Photoreceptor YtvA: A Combined Experimental and Theoretical Study

The light‐induced processes of two flavin mononucleotide derivatives (1‐ and 5‐deaza flavin mononucleotide, 1DFMN and 5DFMN), incorporated into the LOV domain of YtvA protein from Bacillus subtilis, were studied by a combination of experimental and computational methods. Quantum mechanics/molecular mechanics (QM/MM) calculations were carried out in which the QM part was treated by density functional theory (DFT) using the B3LYP functional for geometry optimizations and the DFT/MRCI method for spectroscopic properties, whereas the MM part was described by the CHARMM force field. 1DFMN is incorporated into the protein binding site, yielding a red‐shifted absorption band (λ_max=530 nm compared to YtvA wild‐type λ_max=445 nm), but does not undergo any LOV‐typical photoreactions such as triplet and photoadduct formation. QM/MM computations confirmed the absence of a channel for triplet formation and located a radiation‐free channel (through an S₁/S₀ conical intersection) along a hydrogen transfer path that might allow for fast deactivation. By contrast, 5DFMN‐YtvA‐LOV shows a blue‐shifted absorption (λ_max=410 nm) and undergoes similar photochemical processes to FMN in the wild‐type protein, both with regard to the photophysics and the formation of a photoadduct with a flavin‐cysteinyl covalent bond. The QM/MM calculations predict a mechanism that involves hydrogen transfer in the T₁ state, followed by intersystem crossing and adduct formation in the S₀ state for the forward reaction. Experimentally, in contrast to wild‐type YtvA, dark‐state recovery in 5DFMN‐YtvA‐LOV is not thermally driven but can only be accomplished after absorption of a second photon by the photoadduct, again via the triplet state. The QM/MM calculations suggest a photochemical mechanism for dark‐state recovery that is accessible only for the adduct with a C4a? S bond but not for alternative adducts with a C5? S bond.     

Enantioenriched Calcium‐(R)‐5,5′,6,6′,7,7′,8,8′‐Octahydro‐BINOL (H8‐BINOL): An Efficient Catalyst for the Creation of a Quaternary Stereocenter#

An efficient catalyst for the creation of a quaternary stereocenter has been developed utilizing easily available, eco‐friendly CaCl₂ and applied for enantioselective carbon‐carbon bond forming reactions. Among the surveyed ligands, it was found that (R)‐5,5′,6,6′,7,7′,8,8′‐octahydro‐BINOL‐Ca ( 2f ) gave maximum ee (72%) with excellent yields.     

Organocatalysts for the Synthesis of Poly(ethylene terephthalate‐co‐isosorbide terephthalate): A Combined Experimental and DFT Study

Organocatalysts are assessed for the insertion of isosorbide, a rigid, biobased diol monomer, into poly(ethylene terephthalate). A sulfonic acid (p‐toluenesulfonic acid—APTS), an amidine base (1,8‐diazabicyclo [5.4.0] undec‐7‐ene—DBU) and a guanidine base (1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene—TBD) successfully catalyze the polymerization. The reaction mechanisms are studied by density functional theory. A bifunctional activation is observed in the presence of the sulfonic acid, the carbonyl moiety being activated via the acidic proton of APTS and the alcohol via the basic oxygen. Regarding DBU, a mechanism based on a basic activation of the alcohol rather than a nucleophilic attack of the catalyst is evidenced. The difference observed between TBD and DBU is attributed to a better H‐bonding ability of the former versus the latter.     

Phase separation and melting behavior in poly(ε‐caprolactone)‐epoxy blends cured by 3,3′‐dimethylmethylene‐di(cyclohexylamine)

The morphology and the melting behavior of poly(ε‐caprolactone)/epoxy blends (PCL/epoxy) have been investigated by SEM and DSC. The mechanism of phase separation varies with the curing temperature and PCL content, which can be deduced from the cured morphology of the blend. Higher temperature leads to lower blend viscosity and a higher curing rate, and the final morphology is determined by the competition of these two factors. The PCL melting behavior of the blend is influenced by the extent of phase separation and crystallization during curing. The dual melting behavior of the PCL blend can be ascribed to the interference of the epoxy, which results in the formation of less perfect PCL crystallites melted at lower temperature. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3107–3114, 2003     

Ring Expansion versus Cyclization in 4‐Oxoazetidine‐2‐ carbaldehydes Catalyzed by Molecular Iodine: Experimental and Theoretical Study in Concert

Molecular iodine (10 mol%) efficiently catalyzes the ring expansion of 4‐oxoazetidine‐2‐carbaldehydes in the presence of tert‐butyldimethylsilyl cyanide, or allylic and propargylic trimethylsilanes to afford protected 5‐functionalized‐3,4‐dihydroxypyrrolidin‐2‐ones with good yield and high diastereoselectivity, through a C3 C4 bond cleavage of the β‐lactam nucleus. Interestingly, in contrast to the iodine‐catalyzed reactions of 3‐alkoxy‐β‐lactam aldehydes which lead to the corresponding γ‐lactam derivatives (rearrangement adducts), the reactions of 3‐aryloxy‐β‐lactam aldehydes under similar conditions gave β‐lactam‐fused chromanes (cyclization adducts) as the sole products, through exclusive electrophilic aromatic substitution involving the C3 aromatic ring and the carbaldehyde. In order to support the mechanistic proposals, theoretical studies have been performed.