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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Synthesis and properties of new luminescent hole transporting materials containing triphenylamine and carbazole units
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Synthesis and properties of new luminescent hole transporting materials containing triphenylamine and carbazole units

机译:含三苯胺和咔唑单元的新型发光空穴传输材料的合成与性能

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Two new blue luminescent hole transporting materials (HTM) containing triphenylamine, carbazole units and olefinic linkers (TM1 and TM2) were synthesized via Wittig reaction and characterized by 1H NMR, FT-IR, and HRMS. The compounds show good solubility in common organic solvents such as dichloromethane, chloroform, tetrahydrofuran and dimethyl formamide. Their optical, electrochemical and crystalline properties were investigated by using UV-Vis, photoluminescence (PL) spectra, cyclic voltammetry (CV) and differential scanning calorimetry (DSC), respectively. Quantum-chemical calculation was performed to obtain their optimized structures and the electron distribution of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels. The UV-Vis absorption and PL spectra of the two compounds in solid state were found to be similar to that when they were in dilute THF, which suggests that these compounds remain as an amorphous state in solid films. CV measurements show that the two compounds embody suitable HOMO levels (in a range of -5.28 to -5.23 eV) for hole injection, which is consistent with the calculation consequence. Two compounds possess high glass-transition temperature (T _g) at 96.61 and 90.74 °C for TM1 and TM2, respectively, suggesting the two compounds could form stable amorphous glassy states. The experimental results show that the synthesized compounds have great potential for application in organic light-emitting devices (OLEDs).
机译:通过Wittig反应合成了两种新的蓝色发光空穴传输材料(HTM),它们分别含有三苯胺,咔唑单元和烯烃连接基(TM1和TM2),并通过1 H NMR,FT-IR和HRMS进行了表征。该化合物在常见的有机溶剂(例如二氯甲烷,氯仿,四氢呋喃和二甲基甲酰胺)中显示出良好的溶解性。分别使用紫外-可见光谱,光致发光(PL)光谱,循环伏安法(CV)和差示扫描量热法(DSC)研究了它们的光学,电化学和晶体性质。进行了量子化学计算,以获得它们的优化结构和最高占据分子轨道(HOMO)和最低未占据分子轨道(LUMO)能级的电子分布。发现这两种化合物在固态下的UV-Vis吸收和PL光谱与在稀THF中时的相似,这表明这些化合物在固态膜中保持为非晶态。 CV测量表明,这两种化合物的空穴注入具有合适的HOMO水平(在-5.28至-5.23 eV范围内),与计算结果一致。两种化合物分别对TM1和TM2具有96.61和90.74°C的高玻璃化转变温度(T _g),表明这两种化合物可形成稳定的非晶态玻璃态。实验结果表明,所合成的化合物具有广阔的应用前景。

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