首页> 外文期刊>Chemistry of heterocyclic compounds >Synthesis, structure, and characterization of high-energy 4,6-diazido-N-(4,6-diazido-1,3,5-triazin-2-yl)-1,3,5-triazin-2-amine
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Synthesis, structure, and characterization of high-energy 4,6-diazido-N-(4,6-diazido-1,3,5-triazin-2-yl)-1,3,5-triazin-2-amine

机译:高能4,6-二氮杂基-N-(4,6-二氮杂-1,3,5-三嗪-2-基胺-2-胺的合成,结构和表征。-1,3,5-三嗪-2-胺

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摘要

The high-energy compound 4,6-diazido-N-(4,6-diazido-1,3,5-triazin-2-yl)-1,3,5-triazin-2-amine was obtained in high yield by azidation of 4,6-dichloro-N-(4,6-dichloro-1,3,5-triazin-2-yl)-1,3,5-triazin-2-amine with sodium azide in acetone. According to D-13 and N-15 NMR spectral data, the obtained tetraazide did not undergo azido-tetrazole tautomerism in DMSO solutions and existed solely in the azide form. This tetraazide formed a molecular 1:1 complex with pyridine, the structure of which was confirmed by X-ray structural analysis. The obtained tetraazide had an exceptionally high melting point among azidotriazines (220-222A degrees D), high enthalpy of formation (1641 kJ/mol) and may be of interest as starting compound for the preparation of new high-energy materials.
机译:高能量化合物4,6-二氮杂基-N-(4,6-二氮杂-1,3,5-三嗪-2-基二氧化铝-2-胺)高产率获得 - 1,3,5-三唑-2-胺获得 将4,6-二氯-N-(4,6-二氯-1,3,5-三唑-2-基二嗪-2-基)-1,3,5-三嗪-2-胺用叠氮酸钠在丙酮中蒸叠。 根据D-13 <倒置感叹号>和N-15 NMR光谱数据,所得四氮化物在DMSO溶液中没有经过氮杂唑级靠近的氮杂物质,并仅存在叠氮化物形式中。 该四氮化物与吡啶形成分子1:1络合物,其结构通过X射线结构分析证实。 所得四氮化物在氮氧化嗪(220-222A度D <倒置感光>)中具有出色的熔点,形成高焓(1641kJ / mol),并且可能是用于制备新型高能量材料的起始化合物 。

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