前所未有的单向手性发光和自组装形态介导的金(I)基对映体的多种圆极化磷光

IF 13.7 Q1 CHEMISTRY, MULTIDISCIPLINARY
Debin Fu, Shanting Liu, Xiaofei Yang, Zhao Chen, Sheng Hua Liu
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引用次数: 0

摘要

用手性发光分子在相同条件下实现具有相同手性方向的圆偏振发光是前所未有的。同时,获得具有较大不对称因子(glum)的圆偏振磷光(CPP)具有重要意义,但具有一定的挑战性。本文制备了两种手性含Au(I)对映体,即(S,S)-1和(R,R)-1。(S,S)-1和(R,R)-1随着溶液中聚集程度的变化表现出不同的自组装行为,从而形成多种CPP信号。值得注意的是,具有+2.78 × 10−2和- 1.54 × 10−2高glum值的非镜像CPP,两种手性Au(I)发光源的手性扩增和反转伴随着其自组装形态的变化。令人印象深刻的是,(S,S)-1和(R,R)-1表现出具有相同手性方向的聚集诱导CPP,这是第一次在相同的外部环境下观察到手性对映体的单向CPL。幸运地得到了它们各自具有不同排列方式的(S,S)-1和(R,R)-1三个多晶晶体。由(S,S)-1或(R,R)-1衍生出的多晶体表现出m -螺旋和p -螺旋的堆叠排列。通过研究(S,S)-1和(R,R)-1培养的六种晶体的CPP特性、堆叠模式和分子间相互作用,进一步了解(S,S)-1和(R,R)-1自组装形态依赖的多模式CPP特性的机制。此外,(S,S)-1和(R,R)-1均表现出力触发CPP猝灭的特征,并且将合成的对映体与商品化的非手性液晶结合得到|胶|值达到0.11的手性共组装体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unprecedented Unidirectional Chiral Luminescence and Self-Assembly Morphologies-Mediated Multifarious Circularly Polarized Phosphorescence From Au(I)-Based Enantiomers

Unprecedented Unidirectional Chiral Luminescence and Self-Assembly Morphologies-Mediated Multifarious Circularly Polarized Phosphorescence From Au(I)-Based Enantiomers

Realizing circularly polarized luminescence (CPL) with the same chiral direction by chiral luminogenic molecules under the identical conditions is unprecedented. Meanwhile, obtaining circularly polarized phosphorescence (CPP) with a large dissymmetry factor (glum) is highly significant but rather challenging. Herein, two chiral Au(I)-containing enantiomers, namely (S,S)-1 and (R,R)-1, are prepared. (S,S)-1 and (R,R)-1 show different self-assembly behaviors as the degree of aggregation in solution changes, leading to the formation of a variety of CPP signals. Notably, non-mirror-image CPP, CPP with the high glum values of +2.78 × 10−2 and −1.54 × 10−2, chirality amplification and inversion from the two chiral Au(I) luminogens are accompanied by the variation of their self-assembly morphologies. Impressively, (S,S)-1 and (R,R)-1 exhibit aggregation-induced CPP with the same chiral direction, and this is the first time that the unidirectional CPL from chiral enantiomers under the identical external environment is observed. Their respective three polymorphic crystals of (S,S)-1 and (R,R)-1, each with different packing arrangements, are fortunately obtained. The polymorphs derived from (S,S)-1 or (R,R)-1 demonstrate both M-helix and P-helix stacking arrangements. Through investigating their CPP properties, stacking modes, and intermolecular interactions of these six types of crystals cultivated by (S,S)-1 and (R,R)-1, the mechanism of their self-assembly morphologies-dependent multiple patterns CPP characteristics of (S,S)-1 and (R,R)-1 is further understood. Additionally, both (S,S)-1 and (R,R)-1 show a force-triggered CPP quenching feature, and the chiral co-assembly system with the |glum| value reaching 0.11 is gained by a combination of the synthesized enantiomers and commercial achiral liquid crystal.

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