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Stacking Transformation-Triggered Circularly Polarized Luminescence Reversion in γ-Cyclodextrins-Pyrene Co-Assembly.
Yang, Shijie; Hu, Fengqing; Xu, Tianjing; Lin, Fanjie; Han, Jinsong; Li, Fei.
Afiliação
  • Yang S; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
  • Hu F; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
  • Xu T; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
  • Lin F; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
  • Han J; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
  • Li F; State Key Laboratory of Natural Medicines, College of Engineering, China Pharmaceutical University, Jiangning District, Nanjing, 211198, China.
Chemistry ; 30(55): e202402012, 2024 Oct 01.
Article em En | MEDLINE | ID: mdl-39072899
ABSTRACT
Considerable attention has been directed towards cyclodextrins (CDs) in the creation of co-assembled CPL-active materials, owing to their intrinsic chiral host cavities and synergistic host-guest interactions. However, achieving reversed CPL emission regulation with single-handedness CDs moiety poses a significant challenge. In this study, we have devised a series of γ-CD-based host-guest complexes comprising dual pyrene imidazolium derivatives with multiple linkers, which exhibit reversed circularly polarized emission. We have uncovered that the transformation of excimer stacking within γ-CD/pyrene complexes contributes to the inverted CPL emissions originating from a single-handed chiral host. This research elucidates the phenomenon of (+)- and (-)-circularly polarized excimer emission (CPEE) within γ-CD, arising from right- and left-handed stacking conformations, respectively.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article