Design Strategies for Ratiometric Chemosensors: Modulation of Excitation Energy Transfer at the Energy Donor Site

被引:201
作者
Guliyev, Ruslan [1 ,2 ,3 ]
Coskun, Ali [3 ]
Akkaya, Engin U. [1 ,2 ]
机构
[1] Bilkent Univ, Dept Chem, TR-06800 Ankara, Turkey
[2] Bilkent Univ, UNAM Mat Sci & Nanotechnol Inst, TR-06800 Ankara, Turkey
[3] Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey
关键词
FLUORESCENT CHEMOSENSOR; ELECTRON-TRANSFER; HIGHLY EFFICIENT; MOLECULAR LOGIC; BODIPY DYES; ION; EMISSION; EXCIMER; RECEPTORS; PROBE;
D O I
10.1021/ja902584a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Excitation energy transfer, when coupled to an ion-modulated ICT chromophore, creates novel opportunities in sensing. The direction of energy transfer and the point of ICT modulation can be varied as desired. In our previous work, we have shown that energy transfer efficiency between two energetically coupled fluorophores will be altered by the metal ion binding to the ICT chromophore carrying a ligand. There are two beneficial results: increased pseudo-Stokes shift and expanded dynamic range. Here, we explored the consequences of the modulation of energy transfer efficiency at the energy donor site, in a molecular design which has an ICT type metal ion-sensitive chromophore placed as the energy donor in the dyad. Clear advantages emerge compared to the acceptor site modulation: unaltered emission wavelength in the red end of the visible spectrum, while keeping a large Stokes shift and the ratiometric character.
引用
收藏
页码:9007 / 9013
页数:7
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