Energetic Methylene‐Bridged Furoxan‐Triazole/Tetrazole Hybrids

Design and synthesis of new energetic materials retains its urgency in chemistry and materials science. Herein, rational construction and regioselective synthesis of a series of energetic compounds comprising of a methylene-bridged combination of 1,2,5-oxadiazole and nitrogen-rich azoles (1,2,4-triazole and tetrazole) enriched with additional explosophoric functionalities (nitro and azo moieties) is presented. All target materials were thoroughly characterized using IR and multinuclear NMR (<sup>1</sup>H, <sup>13</sup>C, <sup>14</sup>N, <sup>15</sup>N) NMR spectroscopy, high-resolution mass spectrometry, X-ray diffraction, and differential scanning calorimetry. All synthesized energetic substances showed good thermal stability (up to 239 °C) and low mechanical sensitivity, while their performance reached or exceeded the level of TNT.

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Publication Details

Journal
ChemPlusChem
Published
2024-08-30
DOI
https://doi.org/10.1002/cplu.202400496
Citations
9
Primary Topic
Synthesis of Tetrazole Derivatives
Type
article
Field-Weighted Citation Impact
2.25
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article

Energetic Methylene‐Bridged Furoxan‐Triazole/Tetrazole Hybrids

Алла Н. Пивкина, Alexander V. Shaferov, Константин А. Моногаров, Ivan V. Ananyev et al.
9 citations
ChemPlusChem
Synthesis of Tetrazole Derivatives
2.25
article

Energetic Methylene‐Bridged Furoxan‐Triazole/Tetrazole Hybrids

Алла Н. Пивкина, Alexander V. Shaferov, Константин А. Моногаров, Ivan V. Ananyev, Леонид Л. Ферштат, Igor V. Fomenkov
article en
9 citations

Abstract

Design and synthesis of new energetic materials retains its urgency in chemistry and materials science. Herein, rational construction and regioselective synthesis of a series of energetic compounds comprising of a methylene-bridged combination of 1,2,5-oxadiazole and nitrogen-rich azoles (1,2,4-triazole and tetrazole) enriched with additional explosophoric functionalities (nitro and azo moieties) is presented. All target materials were thoroughly characterized using IR and multinuclear NMR (<sup>1</sup>H, <sup>13</sup>C, <sup>14</sup>N, <sup>15</sup>N) NMR spectroscopy, high-resolution mass spectrometry, X-ray diffraction, and differential scanning calorimetry. All synthesized energetic substances showed good thermal stability (up to 239 °C) and low mechanical sensitivity, while their performance reached or exceeded the level of TNT.

ChemPlusChemVol. 89(12)
National Research University Higher School of Economics (RU), Russian Academy of Sciences (RU), Semenov Institute of Chemical Physics (RU), A. N. Nesmeyanov Institute of Organoelement Compounds (RU), N.D. Zelinsky Institute of Organic Chemistry (RU), NS Kurnakova Institute of General and Inorganic Chemistry (RU)
Openalex Percentile: Top 12%
Synthesis of Tetrazole Derivatives
2.25
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Energetic Methylene‐Bridged Furoxan‐Triazole/Tetrazole Hybrids — Алла Н. Пивкина, Alexander V. Shaferov, et al. · ChemPlusChem (2024) | TGRS Research Map | TGRS