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Energetic Salts Based on Monoanions of N , N ‐Bis(1 H ‐tetrazol‐5‐yl)amine and 5,5′‐Bis(tetrazole)
Author(s) -
Guo Yong,
Tao GuoHong,
Zeng Zhuo,
Gao Haixiang,
Parrish Damon A.,
Shreeve Jean'ne M.
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200902951
Subject(s) - chemistry , barium , nuclear magnetic resonance spectroscopy , triclinic crystal system , tetrazole , crystal structure , crystallography , inorganic chemistry , stereochemistry
Abstract High‐density energetic salts that contain nitrogen‐rich cations and the 5‐(tetrazol‐5‐ylamino)tetrazolate (HBTA − ) or the 5‐(tetrazol‐5‐yl)tetrazolate (HBT − ) anion were readily synthesized by the metathesis reactions of sulfate salts with barium compounds, such as bis[5‐(tetrazol‐5‐ylamino)tetrazolate] (Ba(HBTA) 2 ), barium iminobis(5‐tetrazolate) (BaBTA), or barium 5,5′‐bis(tetrazolate) (BaBT) in aqueous solution. All salts were fully characterized by IR spectroscopy, multinuclear ( 1 H, 13 C, 15 N) NMR spectroscopy, elemental analyses, density, differential scanning calorimetry (DSC), and impact sensitivity. Ba(HBTA) 2 ⋅ 4 H 2 O crystallizes in the triclinic space group P $\bar 1$ , as determined by single‐crystal X‐ray diffraction, with a density of 2.177 g cm −3 . The densities of the other organic energetic salts range between 1.55 and 1.75 g cm −3 as measured by a gas pycnometer. The detonation pressure ( P ) values calculated for these salts range from 19.4 to 33.6 GPa, and the detonation velocities ( ν D ) range from 7677 to 9487 m s −1 , which make them competitive energetic materials. Solid‐state 13 C NMR spectroscopy was used as an effective technique to determine the structure of the products that were obtained from the metathesis reactions of biguanidinium sulfate with barium iminobis(5‐tetrazolate) (BaBTA). Thus, the structure was determined as an HBTA salt by the comparison of its solid‐state 13 C NMR spectroscopy with those of ammonium 5‐(tetrazol‐5‐ylamino)tetrazolate (AHBTA) and diammonium iminobis(5‐tetrazolate) (A 2 BTA).