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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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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。跨境的证据?当亚酞菁环用作光收获单元时,在NMR和光谱中观察到连接偶氮苯部分的CIS异构化。值得注意地,在从CIS→逆转器中移动的恢复开始,从转换→CIS转移,观察到荧光强度的降低,从而从CIS→逆变,这可能归因于非辐射衰减速率的变化。

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