Issue 39, 2017

Synthesis of 1-(2H-tetrazol-5-yl)-5-nitraminotetrazole and its derivatives from 5-aminotetrazole and cyanogen azide: a promising strategy towards the development of C–N linked bistetrazolate energetic materials

Abstract

A series of C–N linked bistetrazolate nitramino compounds, i.e., 1-(2H-tetrazol-5-yl)-5-nitraminotetrazole (2) and its energetic salts (3–8), were successfully prepared from readily available 5-aminotetrazole. All new energetic compounds were fully characterized by IR and NMR spectra and elemental analysis, and six of them (1, 3–7) were further determined by single-crystal X-ray diffraction analysis. The nitrogen contents of these energetic bistetrazolate compounds, ranging from 59.3% (3) to 74.8% (7), are much higher than those of the commonly used high explosives such as RDX (N: 37.8%), HMX (N: 37.8%) and CL-20 (N: 38.3%). And theoretical calculations by using the Gaussian 09 program package demonstrate that compounds 1–8 have high positive heats of formation, of which the heats of formation of ammonium salt 4 (3.60 kJ g−1), aminonitroguanidinium 5 (3.11 kJ g−1) and dihydrazinium salt 7 (3.25 kJ g−1) are approximately eight times higher than those of RDX (0.39 kJ g−1) and HMX (0.39 kJ g−1), and four times higher than that of CL-20 (0.83 kJ g−1). The high nitrogen contents and high heats of formation have endowed these energetic compounds with prominent detonation performance. It is noteworthy that compound 7 exhibits an excellent calculated detonation velocity of 9822 m s−1 superior to that of CL-20 (9730 m s−1), while the impact and friction sensitivities of 7 (IS = 8 J, FS = 192 N) are comparable to those of HMX (IS = 7 J, FS = 112 N). The good detonation properties with moderate sensitivities demonstrate that compound 7 is a promising candidate for application as a high-performance energetic material.

Graphical abstract: Synthesis of 1-(2H-tetrazol-5-yl)-5-nitraminotetrazole and its derivatives from 5-aminotetrazole and cyanogen azide: a promising strategy towards the development of C–N linked bistetrazolate energetic materials

Supplementary files

Article information

Article type
Paper
Submitted
07 Jul 2017
Accepted
12 Sep 2017
First published
12 Sep 2017

J. Mater. Chem. A, 2017,5, 20867-20873

Synthesis of 1-(2H-tetrazol-5-yl)-5-nitraminotetrazole and its derivatives from 5-aminotetrazole and cyanogen azide: a promising strategy towards the development of C–N linked bistetrazolate energetic materials

B. Wang, X. Qi, W. Zhang, K. Wang, W. Li and Q. Zhang, J. Mater. Chem. A, 2017, 5, 20867 DOI: 10.1039/C7TA05905A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements