LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Functionalization of fluorodinitroethylamino derivatives based on azole: a new family of insensitive energetic materials

Photo by hansonluu from unsplash

In this work, four energetic N-fluorodinitroethyl-substituted aminoazoles 6, 8, 10 and 11, as well as nitramine 7 and 9 (the N-nitration products of 6 and 8, respectively) are synthesized. All… Click to show full abstract

In this work, four energetic N-fluorodinitroethyl-substituted aminoazoles 6, 8, 10 and 11, as well as nitramine 7 and 9 (the N-nitration products of 6 and 8, respectively) are synthesized. All compounds are characterized by multinuclear NMR spectroscopy, IR, elemental analysis, as well as differential scanning calorimetry (DSC); what's more, the structures of compounds 6, 9 and 10 are confirmed by single crystal X-ray diffraction. In addition, the sensitivities of 6ā€“10 are measured by standard impact and friction tests. The results indicate that the reported compounds are less sensitive than TNT. The detonation performance based on the calculated heat of formation and experimental densities illustrates that most of the compounds might be of interest for applications as insensitive energetic materials, especially for compounds 7 and 9 (D = 8835 and 8896 m sāˆ’1; P = 35.6 and 36.4 GPa).

Keywords: energetic materials; insensitive energetic; functionalization fluorodinitroethylamino; based azole; fluorodinitroethylamino derivatives; derivatives based

Journal Title: New Journal of Chemistry
Year Published: 2018

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.