Laboratoire Géomatériaux et Environnement, EA 4119, Université Paris-Est Marne-la-Vallée, Marne la Vallée, France.
J Fluoresc. 2011 Nov;21(6):2133-41. doi: 10.1007/s10895-011-0914-3. Epub 2011 Jul 13.
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.
新型稠合噻吩并苯并呋喃(包括噻吩并[3,2-b][1]苯并呋喃(1)、[1]苯并噻吩[3,2-b]呋喃(2)和[1]苯并噻吩[3,2-b][1]苯并呋喃(3))的电子吸收、荧光激发和发射光谱以及荧光量子产率在室温下于十四种不同极性的溶剂中进行了记录。化合物 2 没有荧光。在 298 K 下,在苯中测量了化合物 1-3 的实验基态偶极矩,并将其与相应的理论偶极矩值进行了比较。通过基于 Kawski-Chamma-Viallet 和 McRae 方程的溶剂变色相关,定量研究了这些噻吩并苯并呋喃的电子吸收和荧光光谱对溶剂的影响。这些化合物表现出微弱的负溶剂变色行为,表明它们的偶极矩在激发单重态下略低于基态。还建立了电子吸收和荧光波数以及大多数溶剂中荧光量子产率的 Kamlet-Abboud-Taft 多参数关系,表明发生了特定的溶质-溶剂相互作用。