CNRS UMR, Universit Lille Nord de France, Lille, France.
Chemistry. 2011 Sep 12;17(38):10752-62. doi: 10.1002/chem.201100998.
The synthesis, electrochemical, optical, and cation sensing properties of a bis(macrocyclic) dye 1, in which the benzo-15-crown-5 and phenylazathia-15-crown-5 subunits are linked through a styryl pyridinium moiety, are reported. In this new ditopic receptor, the benzo-15-crown-5 macrocycle acts as a highly selective binding site for alkaline earth metal cations (Mg(II) and Ba(II)), whereas the phenylazathia-15-crown-5 displays a strong binding affinity towards soft heavy-metal cations (Hg(II) and Ag(I)). The pronounced changes of the absorption and fluorescence spectra of this bichromophoric dye observed upon different metal cation addition make the dye suitable for dual-wavelength analysis and offer an enticing potential for multitasking sensors.
报道了一种双大环染料 1 的合成、电化学、光学和阳离子传感性质,其中苯并-15-冠-5 和苯并噻唑-15-冠-5 亚基通过苯乙烯基吡啶鎓部分连接。在这个新的双位点受体中,苯并-15-冠-5 大环作为碱性土金属阳离子(Mg(II)和 Ba(II))的高度选择性结合位点,而苯并噻唑-15-冠-5 对软重金属阳离子(Hg(II)和 Ag(I))表现出很强的结合亲和力。这种双生色团染料在加入不同金属阳离子时观察到的吸收和荧光光谱的显著变化,使得该染料适合于双波长分析,并为多功能传感器提供了诱人的潜力。