Novel copper(II) complexes of two tridentate ONN type ligands: Synthesis, characterization, electrical conductivity and luminescence properties


Gonul I., Burak A. Y., KARACA S., ŞAHİN O., SERİN S.

INORGANICA CHIMICA ACTA, vol.477, pp.75-83, 2018 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 477
  • Publication Date: 2018
  • Doi Number: 10.1016/j.ica.2018.02.026
  • Journal Name: INORGANICA CHIMICA ACTA
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.75-83
  • Çukurova University Affiliated: Yes

Abstract

Herein, we describe the synthesis and characterization of two novel tridentate ONN donor ligands, namely, (E)-2-(((2-(dimethylamino)ethyl)imino)methyl)-6-methoxyphenol (HL1) and (E)-2-(((2-(dimethylamino)ethyl)imino)methyl)-6-ethoxyphenol (HL2), and their copper(II) complexes, [Cu-2(L-1)(2)(CH3COO)(2)] (1), [Cu(L-2)(CH3COO)]center dot 2H(2)O (2). They have been synthesized under conventional methods and characterized by elemental analysis, FT-IR, H-1 NMR, C-11 NMR, ICP-OES, TGA, DSC and GC/MS analysis. For the morphological analysis field emission scanning electron microscopy (FESEM) was used. The geometry of the Cu(II) complexes was determined by single crystal X-ray diffraction analysis. The Cu(II) ions are in distorted square-pyramidal coordination environments. 1 crystallizes in orthorhombic space group, Pbca, while 2 crystallizes in monoclinic space group, P2(1)/c. Effects of different solvents and concentrations on the photoluminescence properties of the 1-2 were investigated. The emission bands bathochromically shifted due to increase of the dipole moments of EtOH to H2O and CHCl3 to DMSO, respectively. As a result of the dynamic quenching, the intensity of 1 was decreased with increasing the concentration in the water. The electrical conductivity complexes 1-2 have been also investigated. (C) 2018 Elsevier B.V. All rights reserved.