145250-81-3Relevant articles and documents
Synthesis, Characterization, and Properties of Energetic Compounds Based on a CH2-Bridged Dinitromethyl Explosophore
Huang, Haifeng,Shi, Yameng,Yu, Yao,Yang, Jun
, p. 113 - 119 (2018)
A series of energetic salts based on the 1,1,3,3-tetranitropropane-1,3-diide (TNP) dianion have been prepared and fully characterized by NMR and IR spectroscopy, elemental analysis, and single-crystal X-ray diffraction. Their thermal stability (Td = 111.0–180.9 °C) and sensitivities to mechanical stimuli (IS = 2–5 J; FS = 80–128 N) have been measured. Additionally, their heats of formation (–369.8 to 347.1 kJ mol–1) and detonation performances (P = 25.0–37.0 GPa; vD = 7675–9104 m s–1) have been calculated.
Cocrystal structure, thermal behavior, and DFT calculations between FOX–7 and 1,10–Phenanthroline
Li, Keyao,Ren, Xiangwen,Fu, Shuqin,Zhu, Jiaping
, p. 26 - 32 (2018)
Cocrystal of FOX–7 (1,1-diamino-2,2-dinitroethene) and Phen (1,10-Phenanthroline) has been synthesized and characterized by X–ray crystallography. The single crystal results show that FOX–7 and its cocrystal were crystallized in the monoclinic space groups P21/n and P21/c, respectively. Thermal stability of FOX–7 and FOX–7·Phen were studied by DSC, the first exothermic peak temperatures (TP) of FOX–7 and FOX–7·Phen occurs at 223.2 and 232.7 °C, respectively; indicating that FOX–7·Phen is more stable than FOX–7. Thermokinetic parameters such as the activation energy Ea and pre-exponential factor A were 321.4 kJ mol?1 and 1.166 × 1033 s?1, respectively. DFT studies including geometry optimization, HOMO-LUMO analysis, Mulliken charge and UV–visible spectral data were also calculated by DFT-B3LYP/6-31 + G** level.
A Halogen-Free Green High Energy Density Oxidizer from H-FOX
Dharavath, Srinivas,Tang, Yongxing,Kumar, Dheeraj,Mitchell, Lauren A.,Parrish, Damon A.,Shreeve, Jean'ne M.
, p. 3142 - 3145 (2019)
Reaction of H-FOX (1-hydrazinyl-2,2-dinitroethenamine) with 2,2,2-trinitroethanol resulted in an unexpected compound, 1,1′-methylenebis[3-(2,2,2-trinitroethyl)urea] (5), which when treated with acetic anhydride and 100 % nitric acid gave an N-NO2 derivative, 1,1′-methylenebis[1-nitro-3-(2,2,2-trinitroethyl)urea] (6) in good yield. Compound 6 exhibits a good oxygen balance (+20.4 %), density (d = 1.87 g/cm3) and excellent detonation performance (vD = 8910 m/s; P = 35.8 GPa) as well as acceptable stability and sensitivity, which suggests it as an attractive replacement for ammonium perchlorate (AP).
On the synthesis of 1,1-diamino-2,2-dinitroethene (FOX-7) by nitration of 4,6-dihydroxy-2-methylpyrimidine
Latypov, Nikolaj V.,Johansson, Martin,Holmgren, Erik,Sizova, Ekaterina V.,Sizov, Vladimir V.,Bellamy, Anthony J.
, p. 56 - 59 (2007)
The synthesis of 1,1-diamino-2,2-dinitroethene (FOX-7) by nitration of 4,6-dihydroxy-2-methylpyrimidine and hydrolysis of the resulting intermediate 2-dinitromethylene-5,5-dinitropy-rimidine-4,6-dione has been studied. By varying the reaction parameters the optimal conditions for the synthesis of FOX-7 have been identified and gave a >90% yield of the pure product. The optimised process allowed the spent acid to be recycled without loss of yield, with almost stoichiometric consumption of nitric acid. The purity of the FOX-7 has been determined using a newly developed HPLC method
The unimolecular chemistry of protonated and deprotonated 2, 2-dinitroethene-1, 1-diamine (FOX-7) studied by tandem mass spectrometry and computational chemistry
Zabka, Jan,Simkova, Ludmila,Jalovy, Zdenek,Polasek, Miroslav
, p. 233 - 247 (2014)
2, 2-Dinitroethene-1, 1-diamine (FOX-7) was studied by means of electrospray ionization (ESI) and chemical ionization (CI) mass spectrometry in both positive and negative ion mode. Detailed mechanisms of unimolecular fragmentations of protonated and deprotonated FOX-7 were investigated using high- and low-energy collision-induced dissociation (CID) mass spectrometry, neutral fragment reionization mass spectrometry and quantum chemistry calculations. In deprotonated FOX-7, elimination of the carbodiimide molecule was identified as the energetically most favored fragmentation channel, closely resembling the base hydrolysis of FOX-7. The dinitromethanide ion is formed during this fragmentation as revealed by comparison with CID mass spectra of an isobaric ion prepared by the ESI of authentic sodium dinitromethanide. The proton affinity of FOX-7 was estimated as 855 kJ mol-1 by high-accuracy quantum chemistry calculations. This value corresponds to protonation at the C-2 position, though the oxygen-protonated tautomer was found to be nearly isoenergetic in the gas phase. In acetonitrile, the nitro group-protonated FOX-7 was found to be significantly less stable then its C-2 tautomer. These theoretical findings are clearly reflected in differences in fragmentations of ESI- and CI-generated [M + H]+ ions. Interestingly, the consecutive losses of OH· and NO2 · radicals instead of a whole HNO3 molecule were found to account for the most abundant fragment ion in the positive ESI CID mass spectra. In the CI-generated [M + H]+1 and [M+D]+ ions, substantial internal energy effects upon the CID were observed.
Application of [PVI-SO3H]NO3as a novel polymeric nitrating agent with ionic tags in preparation of high-energetic materials
Sepehrmansourie, Hassan,Zarei, Mahmoud,Zolfigol, Mohammad Ali,Mehrzad, Amin,Hafizi-Atabak, Hamid Reza
, p. 8367 - 8374 (2021/03/03)
In this paper, poly(vinyl imidazole) sulfonic acid nitrate [PVI-SO3H]NO3was synthesized and fully characterized. Then, [PVI-SO3H]NO3was applied for the preparation of energetic materials such as 1,1-diamino-2,2-dinitroethene (FOX-7), pentaerythritol tetranitrate (PETN), 1,3,5-trinitro-1,3,5-triazinane (RDX) and trinitrotoluene (TNT). The major advantages of the presented methodology are mild, facile workup, high yields and short reaction times. [PVI-SO3H]NO3is a suitable nitrating agent forin situgeneration of NO2and without using any co-catalysts of the described nitrating reagent.
