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首页> 外文期刊>Tetrahedron >Synthesis and properties of N,N,N′,N′-tetrasubstituted 1,3-bis(5-aminothien-2-yl)azulenes and their application as a hole-injecting material in organic light-emitting devices
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Synthesis and properties of N,N,N′,N′-tetrasubstituted 1,3-bis(5-aminothien-2-yl)azulenes and their application as a hole-injecting material in organic light-emitting devices

机译:N,N,N',N'-四取代的1,3-双(5-氨基噻吩-2-基)az唑酮的合成,性质及其在有机发光器件中作为空穴注入材料的应用

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摘要

Two title compounds, N,N,N′,N′-tetraphenyl-1,3-bis(5-aminothien-2-yl)azulene (3a) and 1,3-bis{5-(9-carbazolyl)thien-2-yl}azulene (3b), were synthesized from 1,3-di(2-thienyl)azulene (4) by a two-step sequence involving bromination and subsequent Pd-catalyzed amination. These compounds were characterized by spectroscopic analyses and the structure of 3a was determined by X-ray crystallographic analysis. Their HOMO energy levels were estimated using their electrochemical oxidation potentials, and these compounds were used as a hole-injecting material in organic light-emitting devices. The device with 3a showed greater durability than that with copper phthalocyanine.
机译:两个标题化合物N,N,N',N'-四苯基-1,3-双(5-氨基噻吩-2-基)az(3a)和1,3-双{5-(9-咔唑基)噻吩-由1,3-二(2-噻吩基)氮杂烯(4)通过包括溴化和随后的Pd催化的氨基化的两步序列合成了2-基}氮杂烯(3b)。通过光谱分析对这些化合物进行表征,并通过X射线晶体学分析确定3a的结构。利用其电化学氧化电势估算其HOMO能级,并将这些化合物用作有机发光器件中的空穴注入材料。具有3a的器件显示出比具有铜酞菁的器件更高的耐久性。

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