Mixed-ligand copper(II) complexes: Investigation of their spectroscopic, catalysis, antimicrobial and potentiometric properties

Mehmet Tümer*, Nihal Deligönül, Ayşegül Gölcü, Eyüp Akgün, Mustafa Dolaz, Havva Demirelli, Metin Dığrak

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

66 Citations (Scopus)

Abstract

Schiff base ligands HL 1 -HL 6 have been prepared from the reaction of 2,6-diformyl-4-t-butylphenol and 2,6-di-formyl-4-methylphenol with various aromatic amines in ethanolic solution. The Schiff base ligands 2,2′-dipyridine (dp) mixed-ligand Cu II complexes have been obtained. Mixed-ligand Cu II complexes containing the dp ligand have ionic nature and they conduct the electricity in solution media. The complexes have been obtained in two different forms: one of them is [Cu 2 (L n )Cl 3 ] (n: 1, 2, 3, 4, 5 and 6) and other complexes have the general formula [Cu 2 (L n )(dp) 2 ]3Cl. Ligands and their complexes have been characterized by elemental analyses, FT-IR, electronic spectra, molar conductance, 1 H( 13 C)-n.m.r. and mass spectral data. Their stoichiometric protonation constants have been determined potentiometrically in dioxan using a combined pH electrode at 25°C, under a nitrogen atmosphere. For the calculation of the protonation constants, PKAS computer programme has been used. The effects of the substituents on the protonation constants and the additivities of these effects are discussed. The antimicrobial activity studies of the ligands and their complexes have been studied against the Bacillus megaterium, Micrococcus luteus, Corynebavterium xenosis, Enterococcuc faecalis, bacteria and Saccoramyces cerevisia, yeast. The catalytic properties of the complexes have been studied on the ascorbic acid, catechol and 2,6-di-t-butylphenol substrates. Thermal behaviour of the complexes has been studied by thermal techniques.

Original languageEnglish
Pages (from-to)1-12
Number of pages12
JournalTransition Metal Chemistry
Volume31
Issue number1
DOIs
Publication statusPublished - Feb 2006
Externally publishedYes

Funding

The present study was financially supported by K.Maras Sutcu Imam University, Head of Research Unit (Project code: 2004/4–5).

FundersFunder number
K.Maras Sutcu Imam University

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