Skip to main navigation Skip to search Skip to main content

Energetic 1,2,5-Oxadiazolo-Pyridazine and its N-Oxide

  • Yongxing Tang
  • , Chunlin He
  • , Gregory H. Imler
  • , Damon A. Parrish
  • , Jean'ne M. Shreeve*
  • *Corresponding author for this work
  • University of Idaho
  • Naval Research Laboratory

Research output: Contribution to journal › Article › peer-review

Abstract

Achieving an energetic compound, which exhibits high performance and insensitivity, is important in the field of energetic materials and remains a major challenge. Herein, we found that oxidation of 4,7-diaminopyridazino[4,5-c]furoxan (5) with a mixture of 50 % hydrogen peroxide and trifluoroacetic anhydride gave 6-amino-7-nitro-[1,2,5]oxadiazolo[3,4-c]pyridazine (7) and its N-oxide derivative (8). The oxidation of 5 with hypofluorous acid (HOF) was also studied. Compound 8 displayed an energetic performance compared to triaminotrinitrobenzene (TATB) and insensitive properties (impact sensitivity (IS) 36 J and friction sensitivity (FS)>360 N). Such excellent properties make 8 attractive for high-performance applications, in which insensitivity is important.

Original languageEnglish
Pages (from-to)15022-15025
Number of pages4
JournalChemistry - A European Journal
Volume23
Issue number60
DOIs
Publication statusPublished - 26 Oct 2017
Externally publishedYes

Keywords

  • N-oxides
  • energetic materials
  • furazanes
  • furoxanes
  • pyridazines

Fingerprint

Dive into the research topics of 'Energetic 1,2,5-Oxadiazolo-Pyridazine and its N-Oxide'. Together they form a unique fingerprint.

Cite this