Issue 8, 2013

4-Chloro-3,5-dinitropyrazole: a precursor for promising insensitive energetic compounds

Abstract

A series of 3,5-dinitropyrazole derivatives was prepared from 4-chloro-3,5-dinitropyrazole in good yields and characterized by IR, 1H, and 13C NMR (some cases 15N NMR) spectroscopy, elemental analysis, and DSC. The structures of 7 and 13 were confirmed by single crystal X-ray diffraction. The impact sensitivity was determined using a standard BAM method, and detonation properties were obtained using experimental densities and calculated heats of formation.

Graphical abstract: 4-Chloro-3,5-dinitropyrazole: a precursor for promising insensitive energetic compounds

Supplementary files

Article information

Article type
Paper
Submitted
04 Dec 2012
Accepted
07 Jan 2013
First published
08 Jan 2013

J. Mater. Chem. A, 2013,1, 2863-2868

4-Chloro-3,5-dinitropyrazole: a precursor for promising insensitive energetic compounds

C. He, J. Zhang, D. A. Parrish and J. M. Shreeve, J. Mater. Chem. A, 2013, 1, 2863 DOI: 10.1039/C2TA01359B

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