Abstract
The azotetrazole moiety represents a great platform for energetic materials, it offers a planar and nitrogen-rich backbone, combined with a high heat of formation, which easily can be functionalized and tuned. Herein, we start from sodium 5-aminotetrazolate and obtain two isomers by substitution reaction with 2-chloroethanol. Azidoethyl and nitratoethyl substituted azo- tetrazoles were finally synthesized by oxidative azo coupling of the respective N-ethyl functionalized 5-aminotetrazole precursors using tert-butyl hypochlorite as reagent. All compounds were analyzed through multicore NMR and IR spectroscopy as well as mass spectrometry. All solid compounds were further investigated using low-temperature X-ray crystallography. The purity was verified by CHNO elemental analysis and the decomposition temperature (DTA) and sensitivities toward impact, friction and electrostatic discharged were determined. Based on the CBS-4M calculation results, the energetic properties were calculated using the EXPLO5 code.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Chemie und Pharmazie > Department Chemie |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 540 Chemie |
ISSN: | 1434-193X |
Sprache: | Englisch |
Dokumenten ID: | 96928 |
Datum der Veröffentlichung auf Open Access LMU: | 05. Jun. 2023, 15:24 |
Letzte Änderungen: | 05. Jun. 2023, 15:24 |