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Synthesis and Spectral Characteristics of Two Novel Intramolecular Charge Transfer Fluorescent Dyes

机译:两种新型分子内电荷转移荧光染料的合成及光谱特性

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1.Introduction The intramolecular charge-transfer compound is one kind of the most important molecule materials which is functionalized by electron-donating (D) and electron-accepting (A) groups through a π-conjugated linker. In this paper, two novel ICT fuorescent dyes were synthesized which were (fluorene-2-yl)(9-ethylcarbazole-3-yl) ketene (compound c) and l-phenyl-3-(fluorenone-2-yl)-5-(9-ethylcarbazole-3-yl) -2-pyrazoline (compound e). Their structures were characterized by Ig, 1H NMR and fluorescence spectra. The polarity parameters of ET (30)[1] and △f following the Lippert-Mataga equation[2] were used to correlate the polarity influence of the solvents and the results indicated that the emission wavelength of the compounds was red-shifted and the Stokes shifts increased with the increase of solvent polarity. In addition, the fluorescence quantum yields of the dyes were obtained.
机译:1.引言分子内电荷转移化合物是一种最重要的分子材料,其通过π-共轭连接基团的供电子基团(D)和受电基团(A)进行功能化。本文合成了两种新颖的ICT荧光染料,分别为(芴-2-基)(9-乙基咔唑-3-基)烯酮(化合物c)和1-苯基-3-(芴酮-2-基)-5 -(9-乙基咔唑-3-基)-2-吡唑啉(化合物e)。它们的结构通过Ig,1 H NMR和荧光光谱表征。遵循Lippert-Mataga方程[2]的ET(30)[1]和△f的极性参数用于关联溶剂的极性影响,结果表明化合物的发射波长发生红移,并且斯托克斯位移随溶剂极性的增加而增加。另外,获得了染料的荧光量子产率。

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