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Synthesis of trifluoromethyl-substituted N-aryl-poly-1,2,3-triazole derivatives

机译:三氟甲基取代的N-芳基-聚1,2,3-三唑衍生物的合成

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摘要

Synthesis, characterization, and physical properties of -CF3 and -NO2 substituted N-aryl-polytriazole derivatives are reported. The molecules are prepared by a reliable Cu-catalyzed [3 + 2]-cycloaddition between -CF3 substituted aryl azides and alkynes followed by a nitration sequence and also the base-promoted nucleophilic displacement of the halo groups by the 1,2,3-triazoles. The compounds are characterized by analytical and spectroscopic methods; the solid state structures of some of the compounds are confirmed by X-ray diffraction techniques. The synthesized materials decompose in the range of 195-308 °C. Most of the -CF3 and -NO2 groups-bearing aryl triazoles exhibit good densities and acceptable detonation characteristics. Some of the fluorine containing polytriazole-bearing compounds showed positive heats of formation.
机译:报道了-CF 3和-NO 2取代的N-芳基-聚三唑衍生物的合成,表征和物理性质。这些分子是通过在-CF3取代的芳基叠氮化物和炔烃之间进行可靠的Cu催化的[3 + 2]环加成而制备的,随后是硝化序列以及卤代基团通过1,2,3-碱促进的亲核取代。三唑。这些化合物通过分析和光谱方法表征; X射线衍射技术证实了某些化合物的固态结构。合成的材料在195-308°C的范围内分解。大部分带有-CF3和-NO2基团的芳基三唑都具有良好的密度和可接受的爆轰特性。一些含氟聚三唑的化合物显示出正的形成热。

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