Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(12), С. 3196 - 3207
Опубликована: Дек. 1, 2024
Язык: Английский
Russian Journal of General Chemistry, Год журнала: 2024, Номер 94(12), С. 3196 - 3207
Опубликована: Дек. 1, 2024
Язык: Английский
Journal of Materials Chemistry A, Год журнала: 2024, Номер unknown
Опубликована: Янв. 1, 2024
Compared with traditional polycyclic-based heterocyclic energetic compounds, the synthesis of fused ring compounds is more challenging since only a few substrates meet structural requirements for cyclization reaction.
Язык: Английский
Процитировано
10Energetic Materials Frontiers, Год журнала: 2024, Номер 5(1), С. 8 - 16
Опубликована: Фев. 23, 2024
In the field of energetic materials, prime attention has been given to synthesis environmentally compatible materials having an adequate balance between energy and stability. For this purpose, nitrogen-rich heterocyclic rings have contributed as pivotal frameworks. Nitro-functionalized 1,2,4-triazoles profusely used a constituent for synthesizing high-performing (EMs) due their high nitrogen content, good thermal stability, modifiable sites via functionalization. Combination with different scaffold may provide opportunity accessible tailoring. work, in effort investigate potential 3-nitrotriazoles, its N-acetonitrile derivative 2 was synthesized, which further converted various explosophores. N-methylene-C bridged asymmetrically connected tetrazole (3) 1,2,4-oxadiazole (9 10) based EMs synthesized. Further tuning properties salt formation strategy employed compounds 4–7, 11 12. 1,2,4-oxadiazole-based compound 9 also confirmed X-ray diffraction analysis, 10 analyzed 15N NMR spectroscopy. Compounds 3, 4, 5, 7 exhibited stabilities were found be insensitive towards impact friction. 6, detonation performance comparable conventional explosive TATB.
Язык: Английский
Процитировано
10Journal of Materials Chemistry A, Год журнала: 2024, Номер 12(36), С. 24188 - 24194
Опубликована: Янв. 1, 2024
H4 ( T d = 365 °C, D 8844 m s −1 ) synthesized in this work possesses both super heat resistance and high explosive properties, strongly supporting it as a candidate for advanced ultra heat-resistant explosives.
Язык: Английский
Процитировано
8Chemical Communications, Год журнала: 2023, Номер 59(65), С. 9864 - 9867
Опубликована: Янв. 1, 2023
The design of heat-resistant energetic compounds generally employs symmetry, planarity, and multi-hydrogen bonds to obtain with high density, good thermal stability, low sensitivity. In this paper, a hydrazine-bridged compound, 6,6'-(hydrazine-1,2-diyl)bis(5-nitropyrimidine-2,4-diamine) (PHP), was designed synthesized the strategy multi-fused conjugated structure constructed by hydrogen bonds. compound featured strong conjugation stability (364 °C). This provides basis for compounds.
Язык: Английский
Процитировано
14Journal of Molecular Structure, Год журнала: 2023, Номер 1293, С. 136321 - 136321
Опубликована: Июль 30, 2023
Язык: Английский
Процитировано
14Dalton Transactions, Год журнала: 2024, Номер 53(42), С. 17179 - 17189
Опубликована: Янв. 1, 2024
A family of new asymmetric N -methylene-C linked nitropyrazoles and 1,2,4-triazol-3-one based thermally stable energetic materials with reduced sensitivity has been synthesized. Background image via Canva.
Язык: Английский
Процитировано
4Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 159133 - 159133
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Organic Letters, Год журнала: 2025, Номер unknown
Опубликована: Март 7, 2025
Heat-resistant energetic compounds are of great importance in the field material chemistry. Here, we report a practical synthesis series fused-ring via combination 1,2,3-triazine N-oxide and 2,4,6-trinitroaniline moieties. Starting from known compound 4,6-diamino-2-chloropyrimidine-5-carbonitrile (1), nucleophilic substitution followed by one-step nitration introduced three nitro groups onto benzene ring moiety, simultaneously. The resulting 4-7 exhibited high decomposition temperature (Td > 250 °C) as well relatively good detonation properties low sensitivities.
Язык: Английский
Процитировано
0Journal of Molecular Structure, Год журнала: 2025, Номер unknown, С. 142027 - 142027
Опубликована: Март 1, 2025
Язык: Английский
Процитировано
0The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 25, 2025
Among all compounds constructed by intramolecular integration, 4 (Td = 321 °C, D 8799 m s-1, IS 35 J) that integrates ortho amino nitro group and tetrazole framework possesses a much better comprehensive performance than most widely used heat-resistant explosive HNS 318 7612 5 J), which suggest it might be candidate for advanced explosive. Compared with 8, isomer shows significant improvement in density, thermal stability sensitivity, may caused the relatively strong structural aromaticity, hydrogen bond large face-to-face π-π interaction surfaces strength.
Язык: Английский
Процитировано
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