Azobis(polynitrophenyl-1,2,5-oxadiazoles) as Heat-Resistant Friction-Insensitive Energetic Materials DOI
Ilya Deltsov, Dmitry B. Vinogradov, Константин А. Моногаров

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 13, 2024

The evolution of energetic materials science presents new challenging tasks associated with the creation advanced technologies for sustainable development future. In this work, a set heat-resistant high-energy incorporating polynitrophenyl-1,2,5-oxadiazole scaffold enriched azo/azoxy moieties have been designed and synthesized. Due to smart combination explosophoric groups 1,2,5-oxadiazole rings, prepared substances excellent thermal stability (up 300 °C), good densities 1.75 g cm–3), high enthalpies formation (340–538 kJ mol–1), combined nitrogen–oxygen content (63–68%). In-depth structural analysis revealed presence strong intra- intermolecular hydrogen bonds in aminodinitrophenyl derivatives, which small deviation electrostatic potential values explains low mechanical sensitivity these materials. At same time, trinitrophenyl-1,2,5-oxadiazoles three adjacent non-coplanar nitro demonstrated higher impact, albeit retaining complete insensitivity friction. overall performance thus exceeds that known explosive hexanitrostilbene. Therefore, newly synthesized family polynitrophenyl-1,2,5-oxadiazoles provides fruitful foundation

Язык: Английский

Exploring the energetic potential of 2,5-disubstituted tetrazoles: a case of 2,5-bis(oxadiazolyl)tetrazoles DOI
Vera A. Sereda,

Ekaterina V. Dubasova,

Ivan V. Ananyev

и другие.

Dalton Transactions, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

The preparation of new energetic materials comprising the poorly explored 2,5-disubstituted tetrazole scaffold as a central structural motif coupled with oxadiazole rings is reported.

Язык: Английский

Процитировано

0

Energetic Nitrated Azole Assemblies: Linear Alliance of Isomeric Furazan-1,2,4-triazole-pyrazole Combinations DOI
Igor L. Dalinger,

T. E. Khoranyan,

Kyrill Yu. Suponitsky

и другие.

Crystal Growth & Design, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 19, 2024

While the effect of isomerism on properties energetic molecules has long been recognized, use this phenomenon to deliberately improve performance materials now approached. Here, we report development effective protocols for preparation isomeric compounds with a furazan-triazole-pyrazole framework, which differ in binding points these subunits and position nitro group. The two synthesized isomers readily form X-ray quality crystals solvates DMSO water, but only one isomer was able give unsolvated crystals. Significant differences molecular geometry noncovalent interactions due solvent incorporated into crystal lattice are highlighted. ambiguity evaluating structure–property relationships single compound from data its solvate is demonstrated. first time, 3-(5-(5-(3,4-dinitro-1H-pyrazol-5-yl)-1H-1,2,4-triazol-3-yl)-4-nitrofurazan (6), greater interest because, unlike other isomer, it not hygroscopic higher density. Isomer 6 shock sensitivity detonation velocity similar those RDX, more thermally stable insensitive friction.

Язык: Английский

Процитировано

2

Energetic azine N-oxides: State-of-the-art achievements in the synthesis and performance DOI
Dmitry B. Vinogradov, Леонид Л. Ферштат

Chemical Engineering Journal, Год журнала: 2024, Номер unknown, С. 158859 - 158859

Опубликована: Дек. 1, 2024

Язык: Английский

Процитировано

2

First Alliance of Pyrazole and Furoxan Leading to High-Performance Energetic Materials DOI

T. E. Khoranyan,

Alexander А. Larin, Kyrill Yu. Suponitsky

и другие.

ACS Applied Materials & Interfaces, Год журнала: 2024, Номер unknown

Опубликована: Сен. 25, 2024

Nitrogen heterocyclic scaffolds retain their leading position as valuable building blocks in material science, particularly for the design of small-molecule energetic materials. However, search more balanced combinations directly linked cores is far from being exhausted and aims to reach ideally high-energy substances. Herein, we present synthetic route novel pyrazole-furoxan framework enriched with nitro groups demonstrate a promising set properties, viz., good thermal stability, acceptable mechanical sensitivity, high detonation performance. In-depth crystal analysis showed that isomers having lower-impact sensitivity values both types regioisomeric pairs are those exocyclic furoxan oxygen atom closer pyrazole ring. Owing favorable combination densities (1.83-1.93 g cm

Язык: Английский

Процитировано

1

Trinitroethyl nitropyrazole-3-carboxylates DOI Creative Commons

Dariya V. Maksimova,

Igor L. Dalinger,

Ирина А. Вацадзе

и другие.

FirePhysChem, Год журнала: 2024, Номер unknown

Опубликована: Окт. 1, 2024

Процитировано

1

Spotlights: Untargeted Forensic Drug Detection, Burn Pit Smoke Inhalation, and Problems in the Friction Sensitivity Literature DOI
Lauren Goulding

ACS Chemical Health & Safety, Год журнала: 2024, Номер 31(4), С. 274 - 275

Опубликована: Июль 3, 2024

Язык: Английский

Процитировано

0

Azobis(polynitrophenyl-1,2,5-oxadiazoles) as Heat-Resistant Friction-Insensitive Energetic Materials DOI
Ilya Deltsov, Dmitry B. Vinogradov, Константин А. Моногаров

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 13, 2024

The evolution of energetic materials science presents new challenging tasks associated with the creation advanced technologies for sustainable development future. In this work, a set heat-resistant high-energy incorporating polynitrophenyl-1,2,5-oxadiazole scaffold enriched azo/azoxy moieties have been designed and synthesized. Due to smart combination explosophoric groups 1,2,5-oxadiazole rings, prepared substances excellent thermal stability (up 300 °C), good densities 1.75 g cm–3), high enthalpies formation (340–538 kJ mol–1), combined nitrogen–oxygen content (63–68%). In-depth structural analysis revealed presence strong intra- intermolecular hydrogen bonds in aminodinitrophenyl derivatives, which small deviation electrostatic potential values explains low mechanical sensitivity these materials. At same time, trinitrophenyl-1,2,5-oxadiazoles three adjacent non-coplanar nitro demonstrated higher impact, albeit retaining complete insensitivity friction. overall performance thus exceeds that known explosive hexanitrostilbene. Therefore, newly synthesized family polynitrophenyl-1,2,5-oxadiazoles provides fruitful foundation

Язык: Английский

Процитировано

0