手性(物理)
发光
分子间力
材料科学
圆极化
超分子化学
圆二色性
荧光
分子
超分子手性
光子学
光电子学
自组装
纳米技术
化学物理
结晶学
聚合物
纳米晶
分子间相互作用
分子物理学
光化学
作者
Dandan Liu,Jiali Chen,Jiao Wu,Zhiwen Wang,Qiao‐Hong Li,Miao Yu,Jian Zhang
标识
DOI:10.1002/anie.202523938
摘要
The development of chiral main-group metal-oxo clusters (MOCs) exhibiting high-performance circularly polarized luminescence (CPL) remains a significant challenge. This study presents a generalizable strategy to successfully synthesize a series of chiral indium-oxo clusters (cInOCs). These cInOCs can further self-assemble into supramolecular absolute helices through intermolecular interactions, exhibiting strong chirality and intense blue CPL with a dissymmetry factor glum of 0.012-0.013. To our knowledge, these cInOCs represent the first intrinsically CPL-active main-group MOCs, whose performance rivals or surpasses that of previously reported dye-doped chiral main-group MOCs systems. Capitalizing on the substantial pore channels within the cInOCs, green and yellow fluorescent dye molecules were encapsulated in situ, yielding cInOCs@Dyes composites with color-tunable CPL properties. Efficient chirality transfer from the cInOC host to the guest dyes led to enhanced and tunable photoluminescence, alongside highly adjustable and amplified CPL. A maximum glum of 0.037 was attained, approximately three times greater than that of the pristine cInOCs. Furthermore, the successful processability of these cInOCs or cInOCs@Dyes composites into flexible, transparent films highlights their considerable potential for practical applications in optical and photonic devices.
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