Liu Zheng-Fei, Liu Xin-Xin, Zhang Han, Zeng Lan, Niu Li-Ya, Chen Peng-Zhong, Fang Wei-Hai, Peng Xiaojun, Cui Ganglong, Yang Qing-Zheng
Key Laboratory of Radiopharmaceuticals, Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, 100875, P. R. China.
State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian, 116024, P. R. China.
Angew Chem Int Ed Engl. 2024 Oct 14;63(42):e202407135. doi: 10.1002/anie.202407135. Epub 2024 Sep 12.
Herein we report on circularly polarized luminescence (CPL) emission originating from supramolecular chirality of organic microcrystals with a |g| value up to 0.11. The microcrystals were prepared from highly emissive difluoroboron β-diketonate (BFdbk) dyes R-1 or S-1 with chiral binaphthol (BINOL) skeletons. R-1 and S-1 exhibit undetectable CPL signals in solution but manifest intense CPL emission in their chiral microcrystals. The chiral superstructures induced by BINOL skeletons were confirmed by single-crystal XRD analysis. Spectral analysis and theoretical calculations indicate that intermolecular electronic coupling, mediated by the asymmetric stacking in the chiral superstructures, effectively alters excited-state electronic structures and facilitates electron transitions perpendicular to BFbdk planes. The coupling increases cosθ from 0.05 (monomer) to 0.86 (tetramer) and triggers intense optical activity of BFbdk. The results demonstrate that optical activity of chromophores within assemblies can be regulated by both orientation and extent of intermolecular electronic couplings.
在此,我们报道了源自有机微晶超分子手性的圆偏振发光(CPL)发射,其|g|值高达0.11。这些微晶由具有手性联萘酚(BINOL)骨架的高发射性二氟硼β-二酮(BFdbk)染料R-1或S-1制备而成。R-1和S-1在溶液中表现出无法检测到的CPL信号,但在其手性微晶中表现出强烈的CPL发射。通过单晶XRD分析证实了由BINOL骨架诱导的手性超结构。光谱分析和理论计算表明,在手性超结构中由不对称堆积介导的分子间电子耦合有效地改变了激发态电子结构,并促进了垂直于BFbdk平面的电子跃迁。这种耦合使cosθ从单体的0.05增加到四聚体的0.86,并引发了BFbdk强烈的光学活性。结果表明,组装体内发色团的光学活性可以通过分子间电子耦合的取向和程度来调节。