Synthesis of energetic triazole- and tetrazole-containing oligomers and polymers
Sign Up to like & getrecommendations! Published in 2017 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-017-2109-6
Abstract: This review covers the synthesis of monomers containing 1,2,3-triazole and/or tetrazole rings and provides analysis of examples where such monomers have been used for the formation of polymers with superior energetic characteristics. The reactions used… read more here.
Keywords: triazole tetrazole; containing oligomers; synthesis energetic; oligomers polymers ... See more keywords
Synthesis and Energetic Properties of N-Substituted 3,4- and 3,5-Dinitropyrazoles
Sign Up to like & getrecommendations! Published in 2023 at "ACS Omega"
DOI: 10.1021/acsomega.2c07390
Abstract: 3,4- and 3,5-Dinitropyrazoles (DNPs) were substituted with acryl and allyl groups on the N1 nitrogen atom, resulting in three novel energetic materials. These compounds are all liquids at room temperature with melting points ranging from… read more here.
Keywords: synthesis energetic; spectroscopy; energetic properties; substituted dinitropyrazoles ... See more keywords
Photoelectrochemical driving and clean synthesis of energetic salts of 5,5′-azotetrazolate at room temperature
Sign Up to like & getrecommendations! Published in 2018 at "Green Chemistry"
DOI: 10.1039/c8gc01663a
Abstract: A photoelectrochemical route with a W, Mo co-doped BiVO4 film photoanode was exploited for the first time to drive the coupling reaction of 5-amino-1H-tetrazole at room temperature for clean synthesis of sodium 5,5′-azotetrazolate, a starting… read more here.
Keywords: room; synthesis energetic; room temperature; clean synthesis ... See more keywords