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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人

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摘要

A series of ten push-pull chromophores comprising 1 H -cyclopenta[ b ]naphthalene-1,3(2 H )-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 (1 H -indene-1,3(2 H )-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 1 H -cyclopenta[ b ]naphthalene-1,3(2 H )-dione has been achieved.
机译:设计,合成了一系列十个包含1 H-环戊[b]萘-1,3(2 H)-二酮作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对其进行了表征,循环伏安法和理论计算。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溶剂溶变色关系发现了所有染料的正溶剂溶变色现象,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,与基于基准茚满-1,3-二酮(1 H-茚-1,3(2 H)-二酮)的类似物系列进行了比较完成了。已经发现在可比的给电子基团下所有染料的分子内电荷转移带都发生了明显的红移。平行于检查不同发色团的光物理性质,已经实现了合成方法的重大改进,该方法使得获得了1 H-环戊[b]萘-1,3(2 H)-二酮。

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