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Photoisomerization and optical properties of a subphthalocyanine-azobenzene-subphthalocyanine triad

机译:亚酞菁 - 偶氮苯 - 亚甲酞菁三合会的光硅酸光学性和光学性质

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摘要

The synthesis and characterization of a subphthalocyanine-azobenzene-subphthalocyanine triad is reported. Evidence for trans <-> cis isomerization of the linking azobenzene moiety is observed in the NMR and optical spectra when the subphthalocyanine rings are used as light-harvesting units. Significantly, a decrease in fluorescence intensity is observed on moving from trans -> cis with a recovery in intensity observed on moving back from cis -> trans that can be attributed to a change in the rate of non-radiative decay.
机译:据报道了亚酞菁 - 偶氮苯甲酯三胞苷的合成和表征。 当将亚酞菁环用作光收集单元时,在NMR和光谱中观察到连接偶氮苯部分的反式偶氮苯异构的证据。 值得注意的是,观察到从反式> CI的转变,在从CIS - >逆变中移动的强度恢复,观察到荧光强度的降低,其可归因于非辐射衰减速率的变化。

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  • 来源
    《RSC Advances》 |2016年第75期|共7页
  • 作者单位

    Nanjing Natl Lab Microstruct State Key Lab Coordinat Chem Nanjing 210046 Jiangsu Peoples R China;

    Nanjing Natl Lab Microstruct State Key Lab Coordinat Chem Nanjing 210046 Jiangsu Peoples R China;

    Nanjing Forestry Univ Coll Chem Engn Jiangsu Key Lab Biomass Based Green Fuels &

    Chem Nanjing 210037 Jiangsu Peoples R China;

    Rhodes Univ Dept Chem POB 94 ZA-6140 Grahamstown South Africa;

    Nanjing Univ Sch Phys Natl Lab Solid State Microstruct Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Univ Sch Phys Natl Lab Solid State Microstruct Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Natl Lab Microstruct State Key Lab Coordinat Chem Nanjing 210046 Jiangsu Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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