Spectral and thermal characterization of salophen type Schiff base and its implementation as solid contact electrode for quantitative monitoring of copper(II) ion

DEMİR S., Yilmaz H., Dilimulati M., Andaç M.

SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, vol.150, pp.523-532, 2015 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 150
  • Publication Date: 2015
  • Doi Number: 10.1016/j.saa.2015.05.093
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.523-532
  • Keywords: Solid contact electrode, Salophen, TD-DFT, ESI-MS, Thermal analyses, Electrochemical impedance spectroscopy, SELECTIVE ELECTRODE, MEMBRANE-ELECTRODE, CRYSTAL-STRUCTURE, COMPLEXES, CHROMIUM(III), LIQUID, SOLUTES
  • Ondokuz Mayıs University Affiliated: Yes


Salophen templated Schiff base 2,3-bis(salicylaldimino)pyridine (H2IF) has been synthesized and fully characterized by a series of different spectroscopic methods and thermogravimetric analysis (TGA). It has been also further probed electrochemically and explored as a cation recognition ionophore in the form of a polymeric membrane as selective sensor for quantitative monitoring of Cu2+. Dielectric properties of the membrane have been studied by electrochemical impedance spectroscopy (EIS). The potentiometric results have demonstrated that the sensor exhibits very good selectivity and sensitivity towards Cu2+ over a wide variety of cations. The electrode has a linear response to Cu2+ with a detection limit of 4.46 x 10(-8) and displays a Nernstian slope (29.14 mV/decade) between pH 3.0 and 6.0 with a fast response time less than 10 s. The solid contact electrodes have been exploited over five mounts period with good reproducibility. The analytical availability of the proposed electrode has been evaluated by applying in the determination of Cu2+ ions in water samples. The structural features and complexation of ionophore with Cu2+ have been monitored by UV-Vis spectroscopy and spectral findings have been further supported by DFT and TD-DFT calculations. (C) 2015 Elsevier B.V. All rights reserved.