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首页> 外文期刊>Chemistry: A European journal >Novel Molecular Building Blocks Based on the Boradiazaindacene Chromophore: Applications in Fluorescent Metallosupramolecular Coordination Polymers
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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 H-1 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.
机译:我们设计和合成了新颖的硼硅氮杂茚并(Bodipy)衍生物,它们适当地功能化了金属离子介导的超分子聚合。因此,是2-叔吡啶基-,2,6-叔吡啶基-的配体。通过Sonogashira偶联合成了双吡啶基官能化的Bodipy染料。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)导致在化学计量上发生聚合,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,以单体金属络合物起主导作用的方式重新建立了动态​​平衡。平衡的位置可以很容易地通过H-1 NMR和荧光光谱法进行监测。不出所料,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。

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