Synthesis and polarity-sensitive fluorescent properties of a novel water-soluble polycyclic aromatic hydrocarbon (PAH)

Author:

Sweet Samantha D.1,Coulson Drew R.1,Giguère Jean-Benoît2,Morin Jean-François2,Wagner Brian D.1

Affiliation:

1. Department of Chemistry, University of Prince Edward Island, Charlottetown, PE C1A 4P3, Canada.

2. Département de Chimie and Centre de Recherche sur les Matériaux Avancés (CERMA), Université Laval, 1045 Ave de la Médecine, Québec, QC G1V 0A6, Canada.

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.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Photochemical reaction of superoxide radicals with 1-naphthol;Canadian Journal of Chemistry;2021-11

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