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Nitrogen-rich salts based on the combination of 1,2,4-triazole and 1,2,3-triazole rings: a facile strategy for fine tuning energetic properties
The synthesis of four neutral 4-nitro-5-(1,2,4-triazol-3-yl)-2 H -1,2,3-triazole compounds in combination with different energetic moieties like amino, nitrimino, nitro, and azo groups is presented. Furthermore, a novel family of energetic salts based on the 4-nitro-5-(5-R-1,2,4-triazol-3-yl)-2 H -1...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (5), p.2239-2248 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The synthesis of four neutral 4-nitro-5-(1,2,4-triazol-3-yl)-2
H
-1,2,3-triazole compounds in combination with different energetic moieties like amino, nitrimino, nitro, and azo groups is presented. Furthermore, a novel family of energetic salts based on the 4-nitro-5-(5-R-1,2,4-triazol-3-yl)-2
H
-1,2,3-triazole (
2
: R = nitrimino;
3
: R = nitro) monoanion and dianion were controllably synthesized. All new compounds were fully characterized by IR and multinuclear NMR spectroscopy, elemental analysis and DSC measurements. The molecular structures of
2
,
3
,
8
and
17
were determined by single-crystal X-ray diffraction. In addition, the heats of formation and detonation performance of all the energetic compounds were calculated using Gaussian 09 and EXPLO5 v6.01 programs, respectively. Both experimental and theoretical evaluations show promising properties for these energetic compounds, such as high density, positive heats of formation, high thermal stabilities, good sensitivities and excellent detonation performances. Among them,
6
,
7
,
14
to
16
,
24
and
25
exhibit favorable overall properties as energetic materials. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C7TA08941D |