摘要
A n-conjugated phenylaza-15-crown-5-triazol-substituted coumarin fluoroionophore 1 was synthesized by cop- per（I）-catalyzed Huisgen alkyne-azide 1,3-dipolar cycloaddition （CuAAC ＂click＂ reaction）. 1 can display selective fluorescence enhancement toward Fe3＋ over Hg2＋, Cr3＋ and the other metal ions in aqueous solution. In sharp con- trast, the fluorescence behavior between Fe3＋ and Hg2＋ is completely reversed in EtOH. That is, Hg2＋ gives the largest fluorescence enhancement over Cr3＋, Fe3＋ and the other metal ions.
A n-conjugated phenylaza-15-crown-5-triazol-substituted coumarin fluoroionophore 1 was synthesized by cop- per（I）-catalyzed Huisgen alkyne-azide 1,3-dipolar cycloaddition （CuAAC ＂click＂ reaction）. 1 can display selective fluorescence enhancement toward Fe3＋ over Hg2＋, Cr3＋ and the other metal ions in aqueous solution. In sharp con- trast, the fluorescence behavior between Fe3＋ and Hg2＋ is completely reversed in EtOH. That is, Hg2＋ gives the largest fluorescence enhancement over Cr3＋, Fe3＋ and the other metal ions.
