Abstract
1-Amino-5-nitriminotetrazole is synthesized for the first time via acid-catalyzed protection of 1,5-diaminotetrazole with acetone followed by aprotic nitration using N2O5 and in situ deprotection. The salts of 1-amino-5-nitriminotetrazolate are synthesized by addition of the corresponding bases. Most of the nitrogen-rich salts show insane explosive properties and compete with the most powerful non-nuclear explosives. The implementation of a fused triazolium cation yields a promising secondary explosive, with high performance but also low sensitivity and high thermal stability. Metal salts (K and Ag) are successfully used to initiate pentaerythritol tetranitrate using a classical detonator setup.
Item Type: | Journal article |
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Faculties: | Chemistry and Pharmacy > Department of Chemistry |
Subjects: | 500 Science > 540 Chemistry |
ISSN: | 2574-0962 |
Language: | English |
Item ID: | 111348 |
Date Deposited: | 02. Apr 2024, 07:25 |
Last Modified: | 02. Apr 2024, 07:25 |