Issue 46, 2018

Asymmetric nitrogen-rich energetic materials resulting from the combination of tetrazolyl, dinitromethyl and (1,2,4-oxadiazol-5-yl)nitroamino groups with furoxan

Abstract

Three classes of nitrogen-rich energetic compounds 7–9 (combination of tetrazolyl, dinitromethyl and furoxan), 12–17 (combination of tetrazolyl, (1,2,4-oxadiazol-5-yl)nitroamino and furoxan) and 20–22 (combination of dinitromethyl, (1,2,4-oxadiazol-5-yl)nitroamino and furoxan) were obtained by selected reactions with 3,4-dicyano-furoxan. All the new compounds were thoroughly characterized by IR, NMR [1H, 13C{1H}], elemental analysis, and differential scanning calorimetry (DSC). Compounds 7, 13, 20 and 22 were also further characterized with single-crystal X-ray diffraction studies. Heats of formation and detonation performances for nine compounds were determined using Gaussian 03 and EXPLO5 v6.01 programs, showing that 15 as a secondary explosive is superior to 1,3,5-trinitrotriazacyclohexane (RDX) and 20 is a promising green primary explosive.

Graphical abstract: Asymmetric nitrogen-rich energetic materials resulting from the combination of tetrazolyl, dinitromethyl and (1,2,4-oxadiazol-5-yl)nitroamino groups with furoxan

Supplementary files

Article information

Article type
Paper
Submitted
07 Sep 2018
Accepted
30 Oct 2018
First published
30 Oct 2018

Dalton Trans., 2018,47, 16558-16566

Author version available

Asymmetric nitrogen-rich energetic materials resulting from the combination of tetrazolyl, dinitromethyl and (1,2,4-oxadiazol-5-yl)nitroamino groups with furoxan

Y. Liu, C. He, Y. Tang, G. H. Imler, D. A. Parrish and J. M. Shreeve, Dalton Trans., 2018, 47, 16558 DOI: 10.1039/C8DT03616K

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