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Click Access to a Cyclodextrin-Based Spatially Confined AIE Material for Hydrogenase Recognition.


ABSTRACT: The spatial confinement of conjugated phenyl rotators is a compulsory requirement for the fluorescence enhancement of aggregation induced emission (AIE) molecules. This work reports a novel spatially confined AIE material by restricting several tetraphenylethylene (TPE) molecules around the primary face of ?-cyclodextrin (CD) via a Cu(I) catalytic 1,3-dipolar cycloaddition reaction (click chemistry). The spatial confinement effect was found to significantly enhance the fluorescence emission when compared with a single TPE modified CD. In addition, the emission maxima took place with the dimethyl sulfoxide volume ratio of 30% in a water mixture, which is remarkably different from traditional AIE molecules. Benefiting from the CD's complexation effect, this material exhibits a selective fluorescence quenching property in certain hydrogenases and can be used as a fluorescence probe for hydrogenase sensing. This demonstrates the potential of the spatially confined AIECD for practical applications.

SUBMITTER: Zhao R 

PROVIDER: S-EPMC5948543 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Click Access to a Cyclodextrin-Based Spatially Confined AIE Material for Hydrogenase Recognition.

Zhao Rui R   Li Bin B   Wang Yong Y   Hu Wenping W  

Sensors (Basel, Switzerland) 20180408 4


The spatial confinement of conjugated phenyl rotators is a compulsory requirement for the fluorescence enhancement of aggregation induced emission (AIE) molecules. This work reports a novel spatially confined AIE material by restricting several tetraphenylethylene (TPE) molecules around the primary face of β-cyclodextrin (CD) via a Cu(I) catalytic 1,3-dipolar cycloaddition reaction (click chemistry). The spatial confinement effect was found to significantly enhance the fluorescence emission when  ...[more]

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