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以咔唑、芴酮等为原料,通过亲核加成等反应合成了两个新型咔唑衍生物:3-亚芴基肼撑亚甲基-N-乙基咔唑和3,6-双(亚芴基肼撑亚甲基)-N-乙基咔唑(a和b).通过红外、核磁和元素分析对所合成的两种化合物的结构进行了表征,并考察了其紫外吸收光谱、荧光光谱、电化学行为和热稳定性.实验结果表明:所合成化合物a和b的薄膜均显示出较强的红色荧光,且均具有明显的聚集诱导发光(Aggregation-Induced Emission,AIE)特性;化合物a和b的电离势分别为5.62和5.65eV,与正电极ITO的功函数相匹配,可有效降低空穴注入的能垒,有利于空穴的传输;化合物a和b的热分解温度分别是310℃和309℃,均具有良好的热稳定性.

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