Kappaun Stefan, Sović Tanja, Stelzer Franz, Pogantsch Alexander, Zojer Egbert, Slugovc Christian
Institute of Chemistry and Technology of Organic Materials (ICTOS), Graz University of Technology, Stremayrgasse 16, A-8010, Graz, Austria.
Org Biomol Chem. 2006 Apr 21;4(8):1503-11. doi: 10.1039/b600912c. Epub 2006 Mar 14.
Three 5,7-pi-extended 8-benzyloxyquinolines, namely 5,7-diphenyl-, 5,7-bis(biphenyl-4-yl)- and 5,7-bis(4-dibenzothiophenyl)-8-benzyloxyquinoline were prepared and investigated as fluorescent pH-probes in nonaqueous solution. Absorption and photoluminescence spectra of the introduced compounds also including the starting material 8-benzyloxy-5,7-dibromoquinoline as well as their N-protonated counterparts were recorded and the results were rationalized by quantum-chemical calculations. A pronounced red shift of the emission occurred upon protonation of the non halogenated derivatives, while the dibromo-derivative is hardly emissive and is virtually not protonated under the conditions used. The diphenyl- and the bis(biphenyl)-derivative especially show promising photoluminescence quantum yields both in the parent and the protonated state making them candidates for the active component in pH sensing applications.
制备了三种5,7-π扩展的8-苄氧基喹啉,即5,7-二苯基-、5,7-双(联苯-4-基)-和5,7-双(4-二苯并噻吩基)-8-苄氧基喹啉,并将其作为非水溶液中的荧光pH探针进行了研究。记录了所引入化合物(还包括起始原料8-苄氧基-5,7-二溴喹啉)及其N-质子化对应物的吸收光谱和光致发光光谱,并通过量子化学计算对结果进行了合理解释。非卤代衍生物质子化后发射光谱发生明显红移,而二溴衍生物几乎不发光,在所使用的条件下几乎不被质子化。二苯基和双(联苯)衍生物在母体和质子化状态下均表现出有前景的光致发光量子产率,使其成为pH传感应用中活性成分的候选物。