Issue 7, 2016

Novel anthracene- and pyridine-containing Schiff base probe for selective “off–on” fluorescent determination of Cu2+ ions towards live cell application

Abstract

The novel anthracene- and pyridine-containing Schiff base derivative 2-(2-(anthracen-9-ylmethylene)hydrazinyl)pyridine (AP) has been synthesized via one-pot reaction and its fluorescent “off–on” detection of Cu2+ ions, via PET-based mechanism, is reported. The 1 : 1 stoichiometry of AP⋯Cu2+ sensor complex was calculated from Job's plot based on PL titrations and supported by ESI (+Ve) mass spectral analysis. In addition, the binding sites of AP⋯Cu2+ sensor conjugate were supported by 1H NMR titration. The detection limit (LOD) and association constant (Ka) of AP⋯Cu2+ complex were obtained by standard deviation and linear fittings. Furthermore, quantum yield (Φf), SEM analysis, pH effect, FTIR interpretation and density functional theory (DFT) studies were conducted for the AP⋯Cu2+ sensing conjugate. More decisively, confocal fluorescence microscopy imaging from Raw264.7 cells indicated that AP could be used as an effective fluorescent probe for the analysis of Cu2+ ions in living cells.

Graphical abstract: Novel anthracene- and pyridine-containing Schiff base probe for selective “off–on” fluorescent determination of Cu2+ ions towards live cell application

Supplementary files

Article information

Article type
Paper
Submitted
11 Nov 2015
Accepted
26 Apr 2016
First published
27 Apr 2016

New J. Chem., 2016,40, 6101-6108

Author version available

Novel anthracene- and pyridine-containing Schiff base probe for selective “off–on” fluorescent determination of Cu2+ ions towards live cell application

T. Simon, M. Shellaiah, V. Srinivasadesikan, C. Lin, F. Ko, K. W. Sun and M. Lin, New J. Chem., 2016, 40, 6101 DOI: 10.1039/C5NJ03168K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements