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Boosting the circularly polarized luminescence of small organic molecules via multi-dimensional morphology control

Achieving a higher dissymmetry factor is a crucial issue in developing circularly polarized luminescence (CPL) materials. Here, by tailoring the solvent composition and the morphology of the same chiral emissive small molecules (R- or S-SPAn), circularly polarized emission with a boosted dissymmetry...

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Detalles Bibliográficos
Autores principales: Ma, Kai, Chen, Wenjie, Jiao, Tifeng, Jin, Xue, Sang, Yutao, Yang, Dong, Zhou, Jin, Liu, Minghua, Duan, Pengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657416/
https://www.ncbi.nlm.nih.gov/pubmed/31391904
http://dx.doi.org/10.1039/c9sc01577a
Descripción
Sumario:Achieving a higher dissymmetry factor is a crucial issue in developing circularly polarized luminescence (CPL) materials. Here, by tailoring the solvent composition and the morphology of the same chiral emissive small molecules (R- or S-SPAn), circularly polarized emission with a boosted dissymmetry factor (two orders) was realized. It was found that by regulating the water fraction in the mixed THF/H(2)O, we were able to achieve kinetic control over association of chiral emissive R- or S-SPAn into various nanostructures with 0D nanospheres, 2D nanoflakes and 3D stacked nanoflakes. These nanostructures are all CPL active. Remarkably, the dissymmetry factors of the nanostructures were significantly enhanced compared to those of the molecules and further boosted in different morphologies, from ∼10(–4) (0D nanospheres) to 10(–3) (2D flake) to ∼10(–2) (3D nanoflakes). The enlarged g(lum) value could be assigned to a good packing induced strong luminescence of an excimer. This strategy provides an efficient way to fabricate higher dissymmetry factor CPL organic nanomaterials by only changing the supramolecular architectures while using the same chiral small molecules.