发色团
堆积
荧光
光化学
共价键
共轭体系
猝灭(荧光)
材料科学
红外线的
双光子激发显微术
化学
光学
聚合物
有机化学
物理
作者
Jin‐Yue Zeng,Xiaoshuang Wang,Bo‐Ru Xie,Minjie Li,Xian‐Zheng Zhang
标识
DOI:10.1002/ange.201912594
摘要
Abstract Fluorescent materials exhibiting two‐photon induction (TPI) are used for nonlinear optics, bioimaging, and phototherapy. Polymerizations of molecular chromophores to form π‐conjugated structures were hindered by the lack of long‐range ordering in the structure and strong π–π stacking between the chromophores. Reported here is the rational design of a benzothiadiazole‐based covalent organic framework (COF) for promoting TPI and obtaining efficient two‐photon induced fluorescence emissions. Characterization and spectroscopic data revealed that the enhancement in TPI performance is attributed to the donor‐π‐acceptor‐π‐donor configuration and regular intervals of the chromophores, the large π‐conjugation domain, and the long‐range order of COF crystals. The crystalline structure of TPI‐COF attenuates the π–π stacking interactions between the layers, and overcomes aggregation‐caused emission quenching of the chromophores for improving near‐infrared two‐photon induced fluorescence imaging.
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