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Photophysical and electrochemical properties of 1,7-diaryl-substituted perylene diimides

机译:1,7-二芳基取代的per二酰亚胺的光物理和电化学性质

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Substituent effects on the photophysical and electrochemical properties of 1,7-diaryl-substituted perylene diimides (1,7-Ar(2)PDIs) have been carefully explored. Progressive red-shifts of the absorption and emission maxima were observed when the electron-donating ability of these substituents was increased. Linear Hammett correlations of 1/lambda(max) versus sigma(+) were observed in both spectral analyses. The positive slopes of the Hammett plots suggested that the electronic transitions carry certain amounts of photoinduced intramolecular charge-transfer (PICT) character from the aryl substituents to the perylene diimide core which leads to the reduction of the electron density on the substituents. The substituent electronic effects originated mainly from the perturbation of the core PDI HOMO energy level by the substituents. This conclusion was supported by PM3 analyses and confirmed by cyclic voltammetry experiments. More interestingly, the Ph2NC6H4-substituted PDI, 4i, showed an unusual dual-band absorption that spans from 450 to 750 nm. We tentatively assigned these two bands as the charge-transfer band and the PDI core absorption, respectively.
机译:仔细研究了取代基对1,7-二芳基取代的per二酰亚胺(1,7-Ar(2)PDIs)的光物理和电化学性能的影响。当这些取代基的给电子能力增加时,观察到吸收和发射最大值的进行性红移。在两个光谱分析中均观察到1 /λ(max)与sigma(+)的线性Hammett相关性。 Hammett图的正斜率表明,电子跃迁具有一定量的从芳基取代基到the二酰亚胺核的光致分子内电荷转移(PICT)特征,这导致取代基上的电子密度降低。取代基的电子效应主要源自取代基对核心PDI HOMO能级的扰动。该结论得到PM3分析的支持,并被循环伏安法实验证实。更有趣的是,Ph2NC6H4取代的PDI 4i显示出异常的双波段吸收,范围从450到750 nm。我们暂时将这两个频带分别指定为电荷转移频带和PDI磁芯吸收。

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