| Literature DB >> 30675973 |
Zuo-Bang Sun1, Jun-Kai Liu2, Da-Fei Yuan2, Zheng-Hua Zhao1, Xiao-Zhang Zhu2, Di-Hong Liu1, Qian Peng2, Cui-Hua Zhao1.
Abstract
Temperature-dependent dual fluorescence and switchable circularly polarized luminescence (CPL) are two highly pursued but challenging properties for small organic molecules (SOMs). We herein disclose a triarylborane π-system based on a 2,2'-diamino-6,6'-diboryl-1,1'-binaphthyl scaffold that can serve as a versatile building block for achieving these two properties by simply choosing different amino groups. BNMe2 -BNaph with less bulky dimethylamino groups displays temperature-dependent dual fluorescence, and can thus be used as a highly sensitive ratiometric fluorescence thermometer. On the other hand, BNPh2 -BNaph with bulky diphenylamino groups exhibits intense fluorescence in both solution and in the solid state. A change of solvent from nonpolar cyclohexane to highly polar MeCN not only shifts the CPL position to much longer wavelength but also inverts the CPL sign. In addition, the complexation of BNPh2 -BNaph with fluoride greatly enhances the CPL intensity.Entities:
Keywords: 1,1′-binaphthyl scaffolds; circularly polarized luminescence; intramolecular charge transfer; temperature-dependent dual fluorescence; triarylboranes
Year: 2019 PMID: 30675973 DOI: 10.1002/anie.201813320
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336