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Clickable azide-functionalized bromoarylaldehydes – synthesis and photophysical characterization

机译:可点击的叠氮化物功能化溴芳醛醛 - 合成和光物理表征

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摘要

Herein, we present a facile synthesis of three azide-functionalized fluorophores and their covalent attachment as triazoles in Huisgen-type cycloadditions with model alkynes. Besides two ortho- and para-bromo-substituted benzaldehydes, the azide functionalization of a fluorene-based structure will be presented. The copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) of the so-synthesized azide-functionalized bromocarbaldehydes with terminal alkynes, exhibiting different degrees of steric demand, was performed in high efficiency. Finally, we investigated the photophysical properties of the azide-functionalized arenes and their covalently linked triazole derivatives to gain deeper insight towards the effect of these covalent linkers on the emission behavior.
机译:在此,我们介绍了三种叠氮化物官能化荧光团的容易合成及其与alkynes型号的Huisgen型环加成的三唑的共价附着。除了两个原子和溴代取代的苯并醛之外,将呈现芴基结构的叠氮化物功能化。铜(I) - 具有末端炔烃的丙烷-Alkyne环加成(Cuaac),具有末端炔烃,其含有末端alkynes,具有较高的效率。最后,我们研究了叠氮化物官能化的芳烃的光物理性质及其共价连接的三唑衍生物,以更深地洞察这些共价接头对排放行为的影响。

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