N-diazo-bridged nitroazoles: Catenated nitrogen-atom chains compatible with nitro functionalities

Ping Yin, Damon A. Parrish, Jean'Ne M. Shreeve*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

84 Citations (Scopus)

Abstract

N-diazo-bridged azoles were synthesized based on oxidative coupling of N-aminoazoles. Incorporation of extended catenated nitrogen-atom chains with nitro groups led to compounds with favorable functional compatibilities. This combination gives rise to a series of high-density energetic materials (HEDMs) with high heats of formation, enhanced densities, positive oxygen balances, and good detonation properties while retaining excellent thermal stabilities and relatively low impact sensitivities. Calculated and experimental studies showed the delicate balance between the length of the nitrogen atom chain, energetic performance, and inherent stability, thus, providing a promising strategy for designing advanced energetic materials.

Original languageEnglish
Pages (from-to)6707-6712
Number of pages6
JournalChemistry - A European Journal
Volume20
Issue number22
DOIs
Publication statusPublished - 26 May 2014
Externally publishedYes

Keywords

  • catenated nitrogen chains
  • energetic properties
  • explosives
  • nitroazoles
  • nitrogen

Fingerprint

Dive into the research topics of 'N-diazo-bridged nitroazoles: Catenated nitrogen-atom chains compatible with nitro functionalities'. Together they form a unique fingerprint.

Cite this