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Complexation Behavior of a Supramolecular Organic Fluorophore Prepared by Solid‐State Co‐Grinding Crystallization Using 2‐Anthracenecarboxylic Acid and (<i>R</i>)‐1‐(2‐Naphthyl)ethylamine and Its Optical Properties
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Citations
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References
2009
Year
Materials ScienceMany Organic FluorophoresOrganic Material ChemistrySupramolecular AssemblyEngineeringOptical PropertiesSelf-assemblyFluorous SynthesisComplexation BehaviorOrganic ChemistryCrystal FormationChemistryNovel Crystalline SupramolecularHybrid MaterialsCrystallographySupramolecular PolymerSolid State
Abstract A novel crystalline supramolecular organic fluorophorehaving a 2 1 ‐helical columnar structure has been prepared by solid‐state co‐grinding crystallization using crystals of 2‐anthracenecarboxylic acid and ( R )‐1‐(2‐naphthyl)ethylamine. Although many organic fluorophores lose their fluorescence in the solid state, this supramolecular organic fluorophore exhibits fluorescence even in the solid state.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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