Journal
CHEMISTRY OF MATERIALS
Volume 20, Issue 13, Pages 4519-4530Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cm8004166
Keywords
-
Ask authors/readers for more resources
I-Methyl-5-nitriminotetrazole (1) was formed by nitration of 1-methyl-5-aminotetrazole, which was obtained by methylation of sodium 5-aminotetrazolate. 1 was deprotonated using potassium hydroxide forming the corresponding potassium salt (2), which was transformed into silver 1-methyl-5-nitriminotetrazolate (3) by the reaction with silver nitrate. Guanidinium (4), I-aminoguanidinium (5), 1,3-diaminoguanidinium (6), 1,3,5-triaminoguanidinium (7), and azidoformamidinium (8) 1-methyl-5nitriminotetrazolate were prepared by metathesis reactions either using 2 and guanidinium perchlorates or 3 and guanidiniurn chlorides under the precipitation of KClO4 or AgCl, respectively. All compounds were fully characterized by single crystal X-ray diffraction, vibrational spectroscopy, multinuclear NMR spectroscopy, elemental analysis, differential scanning calorimetry (DSQ as well as bomb calorimetry. Since the packing of molecules in the solid state influences the properties of materials significantly, a detailed description of the crystal structures of 3, 4, 6, 7, and 8 is given. Using the heats of combustion the heats of formations were calculated to be strongly endothermic. Several detonation parameters like the detonation pressure and detonation velocity were calculated using the EXPL05 software. In addition the sensitivities were tested using the BAM drop hammer and friction tester. With respect to developing newhigh explosives triaminoguanidinium 1-methyl-5-nitriminotetrazolate shows the most promising values and was therefore successfully tested in a Koenen Test (critical diameter :S 10 mm).
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available