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Hole-transporting thiophene-based hydrazones with reactive vinyl groups

机译:具有反应性乙烯基的空穴传输噻吩基

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Synthesis and optical, thermal, electrochemical, and photoelectrical properties of new thiophene-based hydrazones with reactive vinyl groups are reported. The synthesized compounds were characterized by ' H, ~(13)C NMR, IR, UV/vis, fluorescence, mass spectrometries, and cyclic voltammetry. The synthesized thiophene-based hydrazones form glasses with the glass transition temperatures ranging from 15 °C to 72 °C, as it was elucidated by DSC. Cyclic voltammetry measurements showed that all the synthesized dihydrazones are electrochemically stable up to 0.8 V. Their oxidation potentials are in the range of 0.02-0.55 V. Solid state ionization potentials of these compounds were found to be in the range of 4.82-5.35 eV. Time-of-flight hole-drift mobility in the layer of di-(2-(4-vinylbenzyl)-2-phenyl-l-((thiophene-2-yl)methylene))hydrazone approached 10-5 cm2/Vs at high electric field.
机译:报道了具有反应性乙烯基的新型噻吩基的合成,光学,热,电化学和光电性能。通过1 H,〜(13)C NMR,IR,UV / vis,荧光,质谱和循环伏安法对合成的化合物进行表征。合成的噻吩基形成玻璃,其玻璃化转变温度为15℃至72℃,这已通过DSC进行了阐明。循环伏安法测量表明,所有合成的二hydr在高达0.8 V的电压下都是电化学稳定的。它们的氧化电势在0.02-0.55 V范围内。发现这些化合物的固态电离电势在4.82-5.35 eV范围内。二-(2-(4-乙烯基苄基)-2-苯基-1-((噻吩-2-基)亚甲基))hydr层中的飞行时间空穴漂移迁移率接近10-5 cm2 / Vs高电场。

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