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Synthesis, Characterization, and Energetic Properties of Diazido Heteroaromatic High-Nitrogen C-N Compound

机译:重氮基杂芳族高氮C-N化合物的合成,表征和能量性质

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摘要

The synthesis, characterization, and energetic properties of diazido heteroaromatic high-nitrogen C-N compound, 3,6-diazido-1,2,4,5-tetrazine (DiAT), are reported. Its normalized heat of formation (NΔH_f), experimentally determined using an additive method, is shown to be the highest positive NΔH_f compared to all other organic molecules. The unexpected azido-tetrazolo tautomerizations and irreversible tetrazolo transformation of DiAT are remarkable compared to all other polyazido heteroaromatic high-nitrogen C-N compounds, for example, 2,4,6-triazido-1,3,5-triazine; 4,4′,6,6′-tetra(azido)hydrazo-1,3,5-triazine; 4,4′,6,6′-tetra(azido)azo-1,3,5-triazine; and 2,5,8-tri(azido)-1,3,4,6,7,9,9b-heptaazaphenalene (heptazine).
机译:报道了叠氮基杂芳族高氮C-N化合物3,6-二叠氮基1,2,4,5-四嗪(DiAT)的合成,表征和高能性能。与所有其他有机分子相比,使用加成法实验确定的归一化形成热(NΔH_f)显示为最高正NΔH_f。与所有其他多叠氮基杂芳族高氮C-N化合物(例如2,4,6-三叠氮基-1,3,5-三嗪)相比,DiAT的意想不到的叠氮-四唑基互变异构和不可逆的四唑基转化效果显着。 4,4',6,6'-四(叠氮基)hydr-1,3,5-三嗪; 4,4',6,6'-四(叠氮基)偶氮-1,3,5-三嗪;和2,5,8-三(叠氮基)-1,3,4,6,7,9,9b-庚七氮杂萘(庚嗪)。

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