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Chiral transcription in self-assembled tetrahedral Eu 4 L 6 chiral cages displaying sizable circularly polarized luminescence

机译:自组装四面体Eu 4 L 6手性笼中的手性转录显示出较大的圆偏振发光

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Predictable stereoselective formation of supramolecular assembly is generally believed to be an important but complicated process. Here, we show that point chirality of a ligand decisively influences its supramolecular assembly behavior. We designed three closely related chiral ligands with different point chiralities, and observe their self-assembly into europium (Eu) tetrametallic tetrahedral cages. One ligand exhibits a highly diastereoselective assembly into homochiral (either ΔΔΔΔ or ΛΛΛΛ) Eu tetrahedral cages whereas the two other ligands, with two different approaches of loosened point chirality, lead to a significant breakdown of the diastereoselectivity to generate a mixture of (ΔΔΔΔ and ΛΛΛΛ) isomers. The cages are highly emissive (luminescence quantum yields of 16(1) to 18(1)%) and exhibit impressive circularly polarized luminescence properties ( g lum : up to 0.16). With in-depth studies, we present an example that correlates the nonlinear enhancement of the chiroptical response to the nonlinearity dependence on point chirality.
机译:通常认为超分子组装体的可预测的立体选择性形成是重要但复杂的过程。在这里,我们表明配体的点手性决定性地影响其超分子组装行为。我们设计了三种具有不同点手性的密切相关的手性配体,并观察它们自组装成euro(Eu)四金属四面体笼。一个配体表现出高度非对映选择性组装到同手性的Eu四面体笼中,而另外两个配体具有两种不同的松散手性手性方法,导致非对映选择性显着分解,从而生成(ΔΔΔΔ和ΛΛΛΛ )异构体。该笼子是高发射率的(发光量子产率为16(1)至18(1)%),并展现出令人印象深刻的圆偏振发光特性(g lum:高达0.16)。通过深入的研究,我们提供了一个示例,该示例将手性响应的非线性增强与点手性的非线性依赖性相关联。

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