What makes efficient circularly polarised luminescence in the condensed phase: aggregation-induced circular dichroism and light emission

发光 圆二色性 荧光 猝灭(荧光) 分子内力 分子 光化学 化学 相(物质) 材料科学 化学物理 结晶学 光电子学 立体化学 光学 物理 有机化学
作者
Jianzhao Liu,Huimin Su,Luming Meng,Yihua Zhao,Chunmei Deng,Jason C. Y. Ng,Ping Lü,Faisal Mahtab,Jacky W. Y. Lam,Xuhui Huang,Hongkai Wu,Kam Sing Wong,Ben Zhong Tang
出处
期刊:Chemical Science [Royal Society of Chemistry]
卷期号:3 (9): 2737-2737 被引量:361
标识
DOI:10.1039/c2sc20382k
摘要

In this contribution, we conceptually present a new avenue to construction of molecular functional materials with high performance of circularly polarised luminescence (CPL) in the condensed phase. A molecule (1) containing luminogenic silole and chiral sugar moieties was synthesized and thoroughly characterized. In a solution of 1, no circular dichroism (CD) and fluorescence emission are observed, but upon molecular aggregation, both the CD and fluorescence are simultaneously turned on, showing aggregation-induced CD (AICD) and emission (AIE) effects. The AICD effect is supported by the fact that the molecules readily assemble into right-handed helical nanoribbons and superhelical ropes when aggregated. The AIE effect boosts the fluorescence quantum efficiency (ΦF) by 136 fold (ΦF, ∼0.6% in the solution versus ∼81.3% in the solid state), which surmounts the serious limitations of aggregation-caused quenching effect encountered by conventional luminescent materials. Time-resolved fluorescence study and theoretical calculation from first principles conclude that restriction of the low-frequency intramolecular motions is responsible for the AIE effect. The helical assemblies of 1 prefer to emit right-handed circularly polarised light and display large CPL dissymmetry factors (gem), whose absolute values are in the range of 0.08–0.32 and are two orders of magnitude higher than those of commonly reported organic materials. We demonstrate for the first time the use of a Teflon-based microfluidic technique for fabrication of the fluorescent pattern. This shows the highest gem of −0.32 possibly due to the enhanced assembling order in the confined microchannel environment. The CPL performance was preserved after more than half year storage under ambient conditions, revealing the excellent spectral stability. Computational simulation was performed to interpret how the molecules in the aggregates interact with each other at the molecular level. Our designed molecule represents the desired molecular functional material for generating efficient CPL in the solid state, and the current study shows the best results among the reported organic conjugated molecular systems in terms of emission efficiency, dissymmetry factor, and spectral stability.
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