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Novel molecular building blocks based on the boradiazaindacene chromophore: Applications in fluorescent metallosupramolecular coordination polymers

机译:基于硼氮杂吲哚发色团的新型分子构件:在荧光金属超分子配位聚合物中的应用

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摘要

We designed and synthesized novel boradiazaindacene (Bodipy) derivatives that are appropriately functionalized for metal-ion-mediated supramolecular polymerization. Thus, ligands for 2-terpyridyl-, 2,6-terpyridyl-, and bipyridyl-functionalized Bodipy dyes were synthesized through Sonogashira couplings. These fluorescent building blocks are responsive to metal ions in a stoichiometry-dependent manner. Octahedral coordinating metal ions such as Zn II result in polymerization at a stoichiometry corresponding to two terpyridyl ligands to one Zn II ion. However, at increased metal ion concentrations, the dynamic equilibria are re-established in such a way that the monomeric metal complex dominates. The position of equilibria can easily be monitored by 1H NMR and fluorescence spectroscopies. As expected, although open-shell Fe II ions form similar complex structures, these cations quench the fluorescence emission of all four functionalized Bodipy ligands. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
机译:我们设计和合成了新颖的硼硅氮杂吲哚(Bodipy)衍生物,这些衍生物可以适当地官能化以用于金属离子介导的超分子聚合。因此,通过Sonogashira偶联合成了2-叔吡啶基-,2,6-叔吡啶基-和联吡啶基官能化的Bodipy染料的配体。这些荧光构件以化学计量依赖的方式响应金属离子。八面体配位金属离子(例如Zn II)导致在化学计量下发生聚合,对应于一个Zn II离子的两个吡啶基配体。然而,在增加的金属离子浓度下,动态平衡以单体金属络合物占主导的方式重新建立。平衡的位置可以很容易地通过1 H NMR和荧光光谱法进行监测。如预期的那样,尽管开壳的Fe II离子形成相似的复杂结构,但这些阳离子可猝灭所有四个功能化Bodipy配体的荧光发射。 ©2009 Wiley-VCH Verlag GmbH&Co. KGaA。

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