4.7 Article

One-pot synthesis of a natural phenol derived fluorescence sensor for Cu(II) and Hg(II) detection

Journal

DYES AND PIGMENTS
Volume 155, Issue -, Pages 100-106

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2018.03.037

Keywords

Catechine; Dopamine; Fluorescence; Copper ions; Mercury ions

Funding

  1. Natural Science Foundation of China [21364010, 51663021]
  2. Bingtuan Innovation Team in Key Areas [2015BD003]
  3. Yangtze River scholar research project of Shihezi University [CJXZ201401]
  4. [CZ027205]

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Development of a high performance molecular fluorescence sensor from natural products for metal ions selective detection is also a great challenge. Herein, catechine-dopamine (C-DA) as a fluorescence sensor, was designed for Cu(II) and Hg(II) selective detection in 100% aqueous solution. C-DA with high fluorescence quantum yield of 10.93% was rapidly synthesized from the reaction between two natural phenols, catechine and dopamine, by a simple one-pot organic solvent free approach. Based on fluorescence on-off, C-DA could linearly detect the Cu(II) and Hg(II) concentrations in a range of 75 nM - 10 mu M and 0.25 mu M - 8 mu M, respectively, and realized the Cu(II) and Hg(II) determination in tap water samples. Moreover, C-DA exhibited strong affinity to Cu(II) and Hg(II) among 15 kinds of metal ions and 9 kinds of anions. The association constants of C-DA-Cu(II) and C-DA-Hg(II) were respectively calculated as 3.21X10(4) M-1 and 3.05X10(4) M-1. Interestingly, although both Cu(II) and Hg(II) formed 1:1 complex to C-DA, they bond to C-DA in a different manner. Cu(II) firstly oxidized the catechol hydroxyl to quinone and was reduced to Cu(I), and then Cu(I) chelated with quinone. Nevertheless, Hg(II) straightly bonded to catechol hydroxyl.

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