Fluorescence enhancement of N2O2-type dipyrrin ligand in two step responding to zinc(II) ion

被引:26
|
作者
Song, Hyesun [1 ]
Rajendiran, Senkuttuvan [1 ]
Koo, Eunhae [2 ]
Min, Byoung Koun [3 ]
Jeong, Soon Kwan [4 ]
Thangadurai, T. Daniel [1 ]
Yoon, Sungho [1 ]
机构
[1] Kookmin Univ, Coll Nat Sci, Dept Bio & Nano Chem, Seoul 136702, South Korea
[2] Korea Inst Ceram Engn & Technol, Bio IT Convergence Ctr, Seoul 153801, South Korea
[3] Hydrogen Energy Res Ctr, Seoul 136791, South Korea
[4] Korea Inst Energy Res, Greenhouse Gas Res Ctr, Taejon 305343, South Korea
基金
新加坡国家研究基金会;
关键词
Dipyrrin; Zinc(II); Ligand complex; Fluorescence enhancement; Detection limit; 2-PHOTON MICROSCOPY; ENERGY-TRANSFER; METAL-IONS; COMPLEXES; STATE; RHODIUM(I); DYNAMICS; SENSORS; DYES;
D O I
10.1016/j.jlumin.2012.06.024
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Fluorescence imaging is well-suited for the live imaging of biological Zn(II), which has no facile spectroscopic or magnetic signature. The successful application of this methodology requires the development of robust Zn(II) imaging agents that display high sensitivity, selectivity and temporal fidelity. In this study. a N2O2-type dipyrrin based bimolecular zinc(II) complex was produced and shown to have sharper, blue-shifted and more enhanced fluorescence emission. An approximate threefold fluorescence enhancement was achieved within the micromolar concentration range, which is an important parameter for Zn(II) detection in vivo. The increase in emission intensity was due to the dominant role of aryl-ring rotation in governing the excited state dynamics and fluorescence properties of the dipyrrin dye. Fluorescence titration showed that the ligand complex exhibited very strong zinc(II) binding affinity when compared to that in the binuclear chloro complex. The fluorescence emission changes in the dipyrrin dye to zinc(II) ion could be observed not only using instruments but also by the naked-eye (violet -> sky blue). (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:3089 / 3092
页数:4
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