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Systematic Control of the Excited-State Dynamics and Carrier-Transport Properties of Functionalized Benzo[ghi]perylene and Coronene Derivatives

机译:功能化苯并per和并戊烯衍生物的激发态动力学和载流子传输特性的系统控制

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摘要

A series of benzo[ghi]perylene (Bp) and coronene (Cor) derivatives substituted with electron-withdrawing methoxycarbonyl (COOMe) or electron-donating methoxyl (MeO) groups was synthesized. The electrochemical, spectroscopic, and photophysical properties of these compounds were investigated by cyclic voltammetry, steady-state and time-resolved spectroscopy, and quantum-yield measurements. Introduction of suitable substituents onto the aromatic rings enabled control of electrochemical and spectroscopic behavior. Examination of excited-state dynamics revealed that fluorescence quantum yields increased with increasing number of COOMe groups in both Bp and Cor derivatives, consistent with the findings of DFT calculations. Single-crystal analysis allowed the performance of fieldeffect transistors containing single crystals of the derivatives to be rationalized.
机译:合成了一系列用吸电子甲氧基羰基(COOMe)或给电子甲氧基(MeO)取代的苯并per(Bp)和苯并(Cor)衍生物。通过循环伏安法,稳态和时间分辨光谱以及量子产率测量研究了这些化合物的电化学,光谱和光物理性质。将合适的取代基引入芳环使得能够控制电化学和光谱行为。激发态动力学的研究表明,随着Bp和Cor衍生物中COOMe基团数量的增加,荧光量子产率增加,这与DFT计算的结果一致。单晶分析允许合理化包含衍生物单晶的场效应晶体管的性能。

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