Dalton Transactions, volume 51, issue 31, pages 11806-11813
Chemistry of 2,5-diaminotetrazole
Publication type: Journal Article
Publication date: 2022-07-15
Journal:
Dalton Transactions
scimago Q1
SJR: 0.697
CiteScore: 6.6
Impact factor: 3.5
ISSN: 14779226, 14779234
PubMed ID:
35861528
Inorganic Chemistry
Abstract
1,5-Diaminotetrazole is one of the most prominent high-nitrogen tetrazole compounds described in the literature. Interestingly the isomer 2,5-diaminotetrazole is nearly undescribed due to its challenging synthetic routes. 2,5-Diaminotetrazol (1) was successfully synthesized via amination of 5-aminotetrazole followed by various purification steps to separate it from isomeric 1,5-diaminotetrazole. In addition to the extensive characterization of 2,5-DAT further derivates by protonation, methylation and amination of the tetrazole ring were synthesized and characterized. The resulting tri-functionalized, ionic tetrazolium derivatives were combined with energetic anions (nitrate, perchlorate, azide, 5,5'-bistetrazole-1,1'-diolate (BTO2-)) to adjust and tune the properties of each compound. All compounds were intensively characterized including IR and multinuclear NMR spectroscopy, thermal analysis through DTA, X-ray diffraction and sensitivity testing. The purity was verified by CHNO elemental analysis and the energetic properties were calculated using the EXPLO5 code and the calculated enthalpy of formation (CBS-4M).
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Profiles