Fluorescence Properties and Dipole Moments of Novel Fused Thienobenzofurans. Solvent and Structural Effects

Journal of Fluorescence - Tập 21 - Trang 2133-2141 - 2011
Jean-Jacques Aaron1,2, Cyril Párkányi3, Alain Adenier2, Caroline Potin2, Zuzana Zajíčková4, Omar R. Martínez3, Jiří Svoboda5, Pavel Pihera5, Petr Váchal5
1Laboratoire Géomatériaux et Environnement (LGE), EA 4119, Université Paris-Est Marne-la-Vallée, Marne la Vallée, France
2Interfaces, Traitements, Organisation et Dynamique des Systèmes (ITODYS), Associé au CNRS, UMR 70–86, Université Paris Diderot, Paris, France
3Department of Chemistry and Biochemistry, Florida Atlantic University, Boca Raton, USA
4Department of Physical Sciences, Barry University, Miami Shores, USA
5Department of Organic Chemistry, Prague Institute of Chemical Technology, Prague 6, Czech Republic

Tóm tắt

The electronic absorption, fluorescence excitation and emission spectra, and fluorescence quantum yields of novel fused thienobenzofurans, including thieno[3,2-b][1]benzofuran (1), [1]benzothieno[3,2-b]furan (2), and [1]benzothieno[3,2-b][1]benzofuran (3), were recorded in fourteen solvents of different polarities at room temperature. Compound 2 was not fluorescent. Experimental ground-state dipole moments of compounds 1–3 were measured in benzene at 298 K and compared with the corresponding theoretical dipole moment values. The solvent effects on the electronic absorption and fluorescence spectra of these thienobenzofurans were quantitatively investigated by means of solvatochromic correlations based on the Kawski-Chamma-Viallet and McRae equations. A weak negative solvatochromic behavior was found for these compounds, showing that their dipole moments are slightly lower in the excited singlet-state than in the ground-state. Kamlet-Abboud-Taft multiparameter relationships were also established for electronic absorption and fluorescence wavenumbers, and fluorescence quantum yields in most solvents, demonstrating the occurrence of specific solute-solvent interactions.

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