The Journal of Organic Chemistry · 2019 · 28 citations · 43 references
Natural SciencesChemistryDrug DiscoveryGreen ChemistryOrganic ChemistryFluorescence SpectroscopyOrganic Electronic MaterialsPhotochemistryChromophore DesignElectron-withdrawing GroupsFluorophore ChemistryFluorophore DesignInfrared EmissionMolecular ChromophoresNear-infrared EmissionOrganic Fluorophores
In the context of molecular engineering of push–pull dipolar dyes, we introduce a structural modification of the well-known electron-accepting group 2-dicyanomethylidene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran (TCF). Introduction of a (benzo[d]thiazol-2-yl) moiety failed, and unexpected structures were obtained. On the other hand, phenylthio and phenylsulfonyl entities were successfully introduced at position 3 of the 2-(dicyanomethylidene)-2,5-dihydrofuran ring, giving access to new electron-acceptor groups and dipolar fluorophores displaying near-infrared emission in solution or in the solid state, brighter than their TCF analogues.
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Fundamental aspects of property tuning in push–pull molecules
Filip Bureš · RSC Advances · 2014 · 751 citations · Full text
Natural Sciences, Chemistry, Physics +12