Abstract

BackgroundPoly nitro aromatic compounds are high energy density materials. Carbon–bonded anionic sigma complexes derived from them have remarkable thermal stability. At present there is a strong requirement for thermally stable insensitive high energy density materials (IHEDMs) in the energetic field which necessitates the present investigation.ResultsThree new carbon–bonded anionic sigma complexes were synthesized from 2-chloro-1,3,5-trinitrobenzene, 1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione (1,3-dimethylbarbituric acid) and bases such as triethanolamine, pyridine and N,N-diethylaniline, characterized by UV–VIS, IR, 1H NMR, 13C NMR and elemental analysis data. Their molecular structures were further ascertained through single crystal X-ray diffraction studies. TGA/DTA testings were undertaken at four different heating rates (5, 10, 20 and 40 K/min) and energy of activation was determined employing Ozawa and Kissinger plots.ConclusionsThe reported carbon–bonded anionic sigma complexes were prepared through single pot synthesis in good yield with high purity. These complexes are molecular salts comprise of cation and anion moieties. Because of the salt–like nature, they are highly stable upto 300°C and decompose in two stages on further heating. They are stable towards impact of 2 kg mass hammer upto height limit (160 cm) of the instrument. The delocalization of the negative charge and various hydrogen bonds noticed in their crystals are the added factors of their thermal stability. The new insensitive high energy density materials of the present findings may receive attention in the field of energetics in future.Graphical A new class of carbon-bonded anionic sigma complexes as insensitive high energy density materials

Highlights

  • Nitro aromatic compounds are high energy density materials

  • As a continuation of our interest in synthesizing insensitive high energy density materials [24] we report in this article a new class of carbon–bonded anionic sigma complexes with 1,3-dimethyl-2,6-dioxo5-(2,4,6-trinitrophenyl)-1,2,3,6-tetrahydropyrimidin–4–olate moiety synthesized from 2-chloro-1,3,5-trinitrobenzene (TNCB), 1,3-dimethylpyrimidine-2,4,6 (1H,3H,5H)-trione [N,N-dimethylbarbituric acid (NDMBA)] and bases such as triethanolamine, pyridine and N,N-diethylaniline as insensitive high energy density materials

  • As nitro groups are present at the ortho and para positions with respect to chloro group, carbanionic sigma complex intermediate is formed followed by elimination of chloro group (SNAr) mechanism, substitution product [5-(2,4,6-trinitrophenyl)-1,3-dimethylbarbituric acid] is formed

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Summary

Results

Three new carbon–bonded anionic sigma complexes were synthesized from 2-chloro-1,3,5-trinitrobenzene, 1,3-dimethylpyrimidine-2,4,6(1H,3H,5H)-trione (1,3-dimethylbarbituric acid) and bases such as triethanolamine, pyridine and N,N-diethylaniline, characterized by UV–VIS, IR, 1H NMR, 13C NMR and elemental analysis data. TGA/DTA testings were undertaken at four different heating rates (5, 10, 20 and 40 K/min) and energy of activation was determined employing Ozawa and Kissinger plots

Conclusions
Background
Results and discussion
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