Tetraanionic nitrogen-rich tetrazole-based energetic salts

dc.contributor.author Srinivas, Dharavath
dc.contributor.author Ghule, Vikas D.
dc.contributor.author Muralidharan, Krishnamurthi
dc.contributor.author Jenkins, H. Donald B.
dc.date.accessioned 2022-03-27T08:33:43Z
dc.date.available 2022-03-27T08:33:43Z
dc.date.issued 2013-01-01
dc.description.abstract 1,1,3,3-Tetra(1H-tetrazol-5-yl)propane-based energetic salts were synthesized in a simple and straightforward manner. The structures of these new salts were determined by 1H and 13C NMR spectroscopy, IR spectroscopy, MS, and elemental analysis. All of these compounds showed good thermal stabilities above 180°C, as confirmed by thermogravimetric- differential thermal analysis (TG-DTA) measurements. Moreover, these salts also exhibited high positive enthalpies of formation, high nitrogen content, good thermal stabilities, and moderate detonation properties. Salty but sweet: 1,1,3,3-Tetra(1H-tetrazol-5-yl)propane-based energetic salts were synthesized in a simple and straightforward manner. These salts showed high positive enthalpies of formation, high nitrogen content, good thermal stabilities, and showed moderate detonation properties. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation Chemistry - An Asian Journal. v.8(5)
dc.identifier.issn 18614728
dc.identifier.uri 10.1002/asia.201300033
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/asia.201300033
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/10770
dc.subject azo compounds
dc.subject energetic compounds
dc.subject heats of formation
dc.subject salt effect
dc.subject tetrazoles
dc.title Tetraanionic nitrogen-rich tetrazole-based energetic salts
dc.type Journal. Article
dspace.entity.type
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