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- W4292830227 endingPage "114227" @default.
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- W4292830227 abstract "A series of alkyl-substituted trifluoromethyl cyanostilbene derivatives were designed, synthesized, and evaluated for their photophysical properties and organogel formation. In water, the molecules exhibit excellent aggregation-induced emission (AIE) properties, and the fluorophores substituted with bis (3,5-trifluoromethyl groups) contribute to the formation of stable organo-gels in ethanol under ambient conditions. Scanning Electron Microscopy (SEM) images of the gels show fiber/rod-like morphology different from the anisotropic morphology obtained in the solution state. Single-crystal XRD reveals favorable non-covalent interactions that aid in forming stable organo-gels, and rheological studies indicate good stability of the orange. The organogels show promise in detecting nitro aromatic compounds such as picric acid both in gel-and sol-state." @default.
- W4292830227 created "2022-08-24" @default.
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- W4292830227 date "2023-01-01" @default.
- W4292830227 modified "2023-10-16" @default.
- W4292830227 title "Functional organogel with α-cyanostilbene scaffold: Aggregation enhanced emission and picric acid sensing" @default.
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- W4292830227 doi "https://doi.org/10.1016/j.jphotochem.2022.114227" @default.
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