Publication | Open Access
Enhanced Two-Photon Absorption with Novel Octupolar Propeller-Shaped Fluorophores Derived from Triphenylamine
249
Citations
39
References
2003
Year
EngineeringMolecular BiologyOrganic ChemistryChemistryLarge Tpa Cross-sectionsTwo-photon AbsorptionPhosphorescence ImagingTriphenylamine CoreBioimagingThermally Activated Delayed FluorescencePhotophysical PropertyBiophysicsPhotonicsPhotochemistryFluorous SynthesisBiophotonicsSupramolecular PhotochemistryNatural SciencesSymmetrical FunctionalizationMultiphoton ProcessPhosphorescence
[structure: see text] Novel octupolar fluorophores derived from the symmetrical functionalization of a triphenylamine core with strong acceptor peripheral groups via phenylene-ethynylene linkers have been synthesized and shown to exhibit high fluorescence quantum yields, very large TPA cross-sections in the red-NIR region, and suitable photostability.
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