Click Access to a Cyclodextrin-Based Spatially Confined AIE Material for Hydrogenase Recognition.
Ontology highlight
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 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 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 fluo
SUBMITTER: Zhao R
PROVIDER: S-EPMC5948543 | biostudies-literature | 2018 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA