Calix[4]arene-based, Hg2+-induced intramolecular fluorescence resonance energy transfer chemosensor

被引:189
作者
Ben Othman, Amel
Lee, Jeong Won
Wu, Jia-Sheng
Kim, Jong Seung
Abidi, Rym
Thuery, Pierre
Strub, Jean Marc
Van Dorsselaer, Alain
Vicens, Jacques
机构
[1] CNRS, ECPM, ULP, IPHC, F-67087 Strasbourg, France
[2] Dankook Univ, Dept Chem, Seoul 140714, South Korea
[3] Korea Univ, Dept Chem, Seoul 130701, South Korea
[4] Univ Bizerte, Fac Sci, Zarzouna 7021, Tunisia
[5] CEA Saclay, SCM, CNRS, URA 331, F-91191 Gif Sur Yvette, France
关键词
SELECTIVE DETECTION; EXCIMER FORMATION; MERCURIC ION; SENSOR; CHEMODOSIMETER; DESIGN; HG2+; PYROPHOSPHATE; RECOGNITION; HG(II);
D O I
10.1021/jo071226o
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] A novel calix[4]arene-based chemosensor I based on Hg2+-induced fluorescence resonance energy transfer (FRET) was synthesized, and its sensing behavior toward metal ions was investigated by UV/vis and fluorescence spectroscopies. Addition of Hg2+ to a CH3CN solution of I gave a significantly enhanced fluorescence at similar to 575 nm via energy transfer (FRET-ON) from the pyrenyl excimer to a ring-opened rhodamine moiety. In contrast, addition of Al3+ induced a distinct increase of pyrenyl excimer emission (similar to 475 nm), while no obvious FRET-ON phenomenon was observed. Different binding behaviors of 1 toward Hg2+ and Al3+ were also proposed for the interesting observation.
引用
收藏
页码:7634 / 7640
页数:7
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