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Push-Pull Chromophores Based on the Naphthalene Scaffold: Potential Candidates for Optoelectronic Applications

机译:基于萘支架的推挽发色团:光电应用的潜在候选对象

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摘要

A series of ten push-pull chromophores comprising 1H-cyclopenta[b]naphthalene-1,3(2H)-dione as the electron-withdrawing group have been designed, synthesized, and characterized by UV-visible absorption and fluorescence spectroscopy, cyclic voltammetry and theoretical calculations. The solvatochromic behavior of the different dyes has been examined in 23 solvents and a positive solvatochromism has been found for all dyes using the Kamlet-Taft solvatochromic relationship, demonstrating the polar form to be stabilized in polar solvents. To establish the interest of this polyaromatic electron acceptor only synthesizable in a multistep procedure, a comparison with the analog series based on the benchmark indane-1,3-dione (1H-indene-1,3(2H)-dione) has been done. A significant red-shift of the intramolecular charge transfer band has been found for all dyes, at a comparable electron-donating group. Parallel to the examination of the photophysical properties of the different chromophores, a major improvement of the synthetic procedure giving access to 1H-cyclopenta[b]naphthalene-1,3(2H)-dione has been achieved.
机译:设计,合成了一系列十个以1H-环戊[b]萘-1,3(2H)-二酮为吸电子基团的推挽生色团,并通过紫外可见吸收和荧光光谱,循环伏安法对其进行了表征。和理论计算。已在23种溶剂中检查了不同染料的溶剂溶变色行为,并使用Kamlet-Taft溶剂溶变色关系对所有染料都发现了正溶剂溶变色现象,表明极性形式在极性溶剂中可以稳定。为了确定仅可通过多步方法合成的这种多芳族电子受体的兴趣,已与基于基准茚满-1,3-二酮(1H-茚-1,3(2H)-二酮)的类似物系列进行了比较。 。已经发现在可比较的给电子基团下,所有染料的分子内电荷转移带均发生明显的红移。平行于检查不同发色团的光物理性质,已实现了对1H-环戊[b]萘-1,3(2H)-二酮的合成方法的重大改进。

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