Synthetic Strategies for C‐Amino 1,2,3‐Triazoles and Their Oxides: A Review DOI Open Access
S. P. Balabanova, Alexey A. Voronin, Andrei V. Churakov

et al.

Journal of Heterocyclic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 12, 2024

ABSTRACT The review is devoted to synthetic methods for the preparation of C ‐amino 1,2,3‐triazoles and their oxides being important precursors in development energetic compounds as well biological, medicinal, organic, bio‐organic, polymer, material chemistry. This research mainly covers papers published after year 1986.

Language: Английский

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

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: unknown, P. 158859 - 158859

Published: Dec. 1, 2024

Language: Английский

Citations

2

Dinitrophenyl-oxadiazole compounds: Design strategy, synthesis, and properties of a series of new melt-cast explosives DOI Creative Commons

Baolong Kuang,

Tingwei Wang, Cong Li

et al.

Defence Technology, Journal Year: 2023, Volume and Issue: 35, P. 100 - 107

Published: Dec. 21, 2023

Melt-cast explosives are the most widely used energetic materials in military composite explosives, researchers have been unremittingly exploring high-energy and insensitive melt-cast explosives. In this work, a series of dinitrophenyl-oxadiazole compounds were designed prepared. These an ideal low melting point (80–97 °C), good detonation performance (detonation velocity D = 6455–6971 m/s, pressure P 18–19 GPa) extreme nature (impact sensitivity ≥60 J, friction >360 N). All these well characterized by nuclear magnetic resonance, fourier transform infrared spectroscopy, elemental analysis. Compounds 2, 3 unambiguously confirmed X-ray single crystal diffraction As result, their overall properties superior to traditional trinitrotoluene (TNT) dinitroanisole (DNAN) which may excellent potential applications

Language: Английский

Citations

5

Equilibrium Molecular Structure of 3-Cyano-4-Amino-1,2,5-Oxadiazole-2-Oxide in the Gas Phase DOI
N. V. Lobanov, Anatolii N. Rykov,

A. V. Stepanova

et al.

Journal of Structural Chemistry, Journal Year: 2024, Volume and Issue: 65(8), P. 1603 - 1611

Published: Aug. 1, 2024

Language: Английский

Citations

1

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

T. E. Khoranyan,

Alexander А. Larin, Kyrill Yu. Suponitsky

et al.

ACS Applied Materials & Interfaces, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 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

Language: Английский

Citations

0

Vicinal Combination of N—NH2 and C—NO2 Benefitting for Low Sensitivity and High Energy Azole Molecules: A Strategy Developed from Isomerization DOI Creative Commons
Yaoyao Linghu, Chaoyang Zhang

Energetic Materials Frontiers, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 1, 2024

Language: Английский

Citations

0

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

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 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

Language: Английский

Citations

0

Synthesis of hybrid molecules based on thioglycolurils and 1,2,5-oxadiazoles via the Eschenmoser sulfide contraction DOI Open Access
Ekaterina E. Vinogradova, Alexander А. Larin, Галина А. Газиева

et al.

Mendeleev Communications, Journal Year: 2024, Volume and Issue: 34(1), P. 122 - 125

Published: Jan. 1, 2024

Language: Английский

Citations

0

Synthetic Strategies for C‐Amino 1,2,3‐Triazoles and Their Oxides: A Review DOI Open Access
S. P. Balabanova, Alexey A. Voronin, Andrei V. Churakov

et al.

Journal of Heterocyclic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 12, 2024

ABSTRACT The review is devoted to synthetic methods for the preparation of C ‐amino 1,2,3‐triazoles and their oxides being important precursors in development energetic compounds as well biological, medicinal, organic, bio‐organic, polymer, material chemistry. This research mainly covers papers published after year 1986.

Language: Английский

Citations

0