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В работе представлены результаты исследования влияния новых высокоазотистых соединений комплекса хлорида никеля на скорость горения пиротехнического состава Fe2O3/Ba(NO3)2/Al. Установлено, что представленные в данной работе соединения проявляют ингибирующие скорость горения свойства. Показана взаимосвязь ингибирующей активности соединений от их структуры и химического состава. The paper presents the results of a study of the effect of new high-nitrogen compounds of the nickel chloride complex on the combustion rate of the Fe2O3/Ba(NO3)2/Al pyrotechnic composition. It has been established that the compounds presented in this work exhibit properties that inhibit the burning rate. The relationship between the inhibitory activity of the compounds and their structure and chemical composition is shown.

Dinitramic acid salts are promising components as oxidizers and burning-rate modifiers of high-energy compositions. However, most of these salts are not free of drawbacks such as hygroscopicity. Therefore, their application under special conditions of use and storage is limited. The synthesis and storage of stable dinitramic acid salts is a topical issue. Here, we synthesized an adduct starting from the nickel salt of dinitramic acid with carbohydrazide and glyoxal to settle the problem of stability and storage of that salt. The chemical composition of the adduct was confirmed by infrared spectroscopy and elemental analysis. The Ni content was determined by atomic emission spectroscopy. Thermogravimetric DSC and TGA analyses showed the adduct to have three decomposition stages. The adduct exhibits a good thermal stability and a low sensitivity to mechanical stimuli. Here, the adduct is demonstrated to be a promising burning-rate inhibitor of pyrotechnic compositions.

Herein, we describe the synthesis of coordination compounds starting from carbohydrazide ((H2NHN)2C=O (CHZ)) and the Zn2+ salt of dinitramic acid (HDN), which are high-nitrogen substances that exhibit properties similar to those of a burning-rate inhibitor of pyrotechnic compositions. This study demonstrates that these compounds react with glyoxal to furnish adducts of metal–organic macrocyclic cages bearing the elements of carbohydrazide, complexing metals and the HDN anion, depending on the ratio of the starting reactants. The assembled macrocyclic cage has “host–guest” properties and is a safe container for the storage of HDN salts. X-ray crystallographic analysis of the resultant coordination compound, [Zn(chz)3(N(NO2)2)2]), indicated that the metal‒ligand association occurs via the N and O atoms of carbohydrazide. The zinc salt of dinitramic acid, which is enclosed into adducts with a macrocycle, is thermally stable and insensitive to mechanical impacts. The complex zinc salt of dinitramide was shown herein to exhibit inhibitory activity towards the burning rate of pyrotechnic compositions.

Here, we report the study results of the nitration of 3,7,10-trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane (THAP) by different nitrating agents such as nitric acid, mixed nitric/sulfuric acids, nitric anhydride, and mixed concentrated nitric acid/acetic anhydride to furnish 3,7,10-trioxo-2-nitro-2,4,6,8,9,11-hexaaza[3.3.3]propellane and 3,7,10-trioxo-2,8-dinitro-2,4,6,8,9,11-hexaaza[3.3.3]propellane, whereas a lactam–lactim rearrangement was found to take place upon vigorous cooling to give 10-hydroxy-2,4,6,8,9,11-hexaazatricyclo[3.3.3.01,5]undec-9-ene-3,7-dione. The two competing reactions, lactam–lactim rearrangement, and nitration were found to take place. The acylation of 3,7,10-trioxo-2,4,6,8,9,11-hexaaza[3.3.3]propellane was examined and the formation conditions of 2,6-di- and 2,6,9-triacetyl-substituted and 3,7,10-trioxo-2,4,6,8,9,11-hexaacetyl-2,4,6,8,9,11-hexaaza[3.3.3]propellane were established. The acetyl derivatives were found to be instable in an acidic medium and to undergo deacylation. The obtained findings correlate well with the quantum-chemical calculations.