4.6 Article

Coumarin-naphthol conjugated Schiff base as a turn-on fluorescent probe for Cu2+ via selective hydrolysis of imine and its application in live cell imaging

Journal

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2016.10.030

Keywords

Fluorescent probe; Coumarin-naphthol conjugate; Schiff base; Imine hydrolysis; Copper ion

Funding

  1. Key Project of National Natural Science Foundation of China [81430092]
  2. Ph.D. Programs Foundation of Ministry of Education of China [20120096130002]
  3. Program for Changjiang Scholars and Innovative Research Team in University [IRT_15R63]
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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An off-on fluorescent probe (CuCIN), coumarin-naphthol linked by an imine group, for detecting Cu2+ in DMSO-HEPES buffer (1:99, v/v) solution was successfully developed. Mechanism studies suggested that CuCIN firstly formed a complex with Cu2+ in a 1:2 metal-to-ligand ratio, and then 60-fold fluorescence enhancement was observed when Cu2+ promoted the imine hydrolysis to release the fluorescence compound 7-diethylaminocoumarin-3-aldehyde. This probe displayed desired properties such as high selectivity toward other metal ions, low detection limit (12.7 nM) and low cytotoxicity. Bio-imaging study revealed that the new probe CuCIN could be applied for imaging living cells with good cell permeability. We hope to apply this probe in the biomedical research field for the imaging of disease-relevant Cu2+. (C) 2016 Elsevier B.V. All rights reserved.

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