1. Synthesis and polarity-sensitive fluorescent properties of a novel water-soluble polycyclic aromatic hydrocarbon (PAH)
- Author
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Samantha D. Sweet, Brian D. Wagner, Drew R. Coulson, Jean-François Morin, and Jean-Benoît Giguère
- Subjects
chemistry.chemical_classification ,Ethylene ,Polarity (international relations) ,Anthanthrene ,Organic Chemistry ,Supramolecular chemistry ,Polycyclic aromatic hydrocarbon ,General Chemistry ,Fluorescence ,Catalysis ,chemistry.chemical_compound ,Water soluble ,chemistry ,Organic chemistry ,Derivative (chemistry) - Abstract
We report the successful synthesis and spectroscopic characterization of a novel, water soluble anthanthrene-based derivative, 6,12-bis(TEG)anthanthrene 3. The presence of the two long ethylene glycol side chains gives this large, six-membered polycyclic aromatic compound a high aqueous solubility. It exhibits UV–vis absorption properties similar to those of anthanthrene itself, indicating that the side chains do not have a significant effect on the electronic structure of the central chromophore. The compound exhibits strong, polarity-sensitive fluorescence in aqueous solution in the blue–green region of the spectrum, with a fluorescence quantum yield of 0.13 and a polarity sensitivity factor (PSF) of 2.0. The utility of this new fluorescent molecule as a probe of supramolecular complexation was demonstrated by its inclusion into the molecular host hydroxypropyl-β-cyclodextrin in aqueous solution. Strictly 1:1 inclusion was observed, with a moderately strong binding constant K of 650 M−1. This new fluorescence probe has significant potential applications in fluorescence-based studies of aqueous biochemical and supramolecular systems.
- Published
- 2021
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