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Synthesis of novel multifunctional carbazole-based molecules and their thermal electrochemical and optical properties

机译:新型多功能咔唑基分子的合成及其热电化学和光学性质

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摘要

Two novel carbazole-based compounds 7a and 7b were synthesised as potential candidates for application in organic electronics. The materials were fully characterised by NMR spectroscopy, mass spectrometry, FTIR, thermogravimetric analysis, differential scanning calorimetry, cyclic voltammetry, and absorption and emission spectroscopy. Compounds 7a and 7b, both of which were amorphous solids, were stable up to 291 °C and 307 °C, respectively. Compounds 7a and 7b show three distinctive absorption bands: high and mid energy bands due to locally excited (LE) transitions and low energy bands due to intramolecular charge transfer (ICT) transitions. In dichloromethane solutions compounds 7a and 7b gave emission maxima at 561 nm and 482 nm with quantum efficiencies of 5.4% and 97.4% ± 10%, respectively. At positive potential, compounds 7a and 7b gave two different oxidation peaks, respectively: quasi-reversible at 0.55 V and 0.71 V, and reversible at 0.84 V and 0.99 V. At negative potentials, compounds 7a and 7b only exhibited an irreversible reduction peak at −1.86 V and −1.93 V, respectively.
机译:合成了两种新的咔唑基化合物7a和7b作为潜在的有机电子应用的潜在候选物。通过NMR光谱,质谱,FTIR,热重分析,差示扫描量热法,循环伏安法和吸收和发射光谱,所述材料完全表征。化合物7a和7b,两者都是无定形固体,分别稳定至291℃和307℃。化合物7a和7b示出了三个独特的吸收带:由于局部激发(Le)过渡和由于分子内电荷转移(ICT)过渡而导致的高和中央带。在二氯甲烷溶液中,化合物7a和7b在561nm和482nm处产生排放最大值,量子效率分别为5.4%和97.4%±10%。在阳性电位下,化合物7a和7b分别产生两种不同的氧化峰:在0.55V和0.71V下进行准可逆,并且在0.84V和0.99V下可逆。在负电位,化合物7a和7b仅在不可逆的减少峰值处表现出不可逆的减少峰值-1.86 v和-1.93 v。

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