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Pulling with the Pentafluorosulfanyl Acceptor in Push Pull Dyes

机译:用五氟氟丁基受体拉动拉动染料

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摘要

A new class of push-pull fluorophores featuring the pentafluorosulfanyl (SF5) group as a potent acceptor has been synthesized. Known for its excellent chemical and thermal stability, the unique SF5 functionality is also strongly electron-withdrawing but at the same time highly lipophilic. We report six new fluorescent dyes, which were characterized by UV-vis/fluorescence spectroscopy, single-crystal X-ray diffraction, and cyclic voltammetry. Notable dye properties include large Stokes shifts (100 nm), pronounced solvatofluorochromic effects arising from intramolecular charge transfer, moderate fluorescence quantum yields in both solutions and thin films, and extensive supramolecular C-H center dot center dot center dot F interactions in their crystalline states. Reversible mechanofluorochromism was also observed in dye 5, where grinding and fuming of a solid sample gave blue- and red-shifted emissions, respectively. Postfunctionalization of dye 3 to afford a pair of strong visible-light absorbers was also demonstrated.
机译:已经合成了一种新的推拉荧光团,其具有戊氟磺基(SF5)组作为有效受体。以其优异的化学和热稳定性而闻名,独特的SF5官能度也是强烈的电子提取,但同时非常亲脂性。我们报告了六种新的荧光染料,其特征在于UV-VIS /荧光光谱,单晶X射线衍射和循环伏安法。值得注意的染料性质包括大型斯托克斯偏移(& 100nm),从分子内电荷转移产生的明显的溶解荧光效应,中等荧光量子产量在溶液和薄膜中,以及其晶体状态的广泛的超分子CH中心点中心点中心点F相互作用。在染料5中也观察到可逆的机械氟铬,其中固体样品的研磨和卷曲分别产生了蓝色和红色偏移的排放。还证明了染料3的染料3所得到的染料3。

著录项

  • 来源
    《The Journal of Organic Chemistry》 |2017年第20期|共13页
  • 作者单位

    Univ Ottawa Dept Chem &

    Biomol Sci 10 Marie Curie Pvt Ottawa ON K1N 6N5 Canada;

    Univ Ottawa Dept Chem &

    Biomol Sci 10 Marie Curie Pvt Ottawa ON K1N 6N5 Canada;

    Univ Ottawa Dept Chem &

    Biomol Sci 10 Marie Curie Pvt Ottawa ON K1N 6N5 Canada;

    Univ Ottawa Dept Chem &

    Biomol Sci 10 Marie Curie Pvt Ottawa ON K1N 6N5 Canada;

    Univ Ottawa Dept Chem &

    Biomol Sci 10 Marie Curie Pvt Ottawa ON K1N 6N5 Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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