Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye

New Ni(II), Cu(II) and Co(II) complexes were synthesized with the bidentate azo-azomethine dye, 4-[(E)-phenyldiazenyl]-2-[(E)-(phenylimino)methyl] phenol (dmpH), which was prepared by the reaction of 2-hydroxy-5-[(E)- phenyldiazenyl]benzaldehyde with aniline in EtOH. The syntheses of the metal chela...

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Main Author: Kurtoglu Nurcan
Format: Article
Language:English
Published: Serbian Chemical Society 2009-01-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909917K.pdf
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author Kurtoglu Nurcan
author_facet Kurtoglu Nurcan
author_sort Kurtoglu Nurcan
collection DOAJ
description New Ni(II), Cu(II) and Co(II) complexes were synthesized with the bidentate azo-azomethine dye, 4-[(E)-phenyldiazenyl]-2-[(E)-(phenylimino)methyl] phenol (dmpH), which was prepared by the reaction of 2-hydroxy-5-[(E)- phenyldiazenyl]benzaldehyde with aniline in EtOH. The syntheses of the metal chelates of the azo-azomethine dye were realized by the precipitation technique. The synthesized metal complexes were characterized by elemental analysis, molar conductance measurements, as well as infrared and UV-Vis spectral data. Based on these characterizations, the metal complexes of the transition metal ions may be formulated as [M(dmp)Cl(H2O)] where M = Ni(II), Cu(II) and Co(II). The metal complexes were formed by the coordination of N and O atoms of the ligand. The molar conductance values of the Ni(II), Cu(II) and Co(II) complexes of the bidentate ligand indicate their non-ionic character. The free ligand and its metal complexes were tested for their in vitro antimicrobial properties against eight bacteria: Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Mycobacterium smegmatis, Pseudomonas aeruginosa, Enterococcus cloacae, Bacillus megaterium, and Micrococcus luteus, and three fungi, Kluyveromyces fragilis, Rhodotorula rubra and Saccharomyces cerevisiae, in order to assess their antimicrobial potential. The [Ni(dmp)Cl(H2O)] chelate exhibited high activity against all the bacteria and fungi, except Rhodotorula rubra.
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spelling doaj.art-5f2973f1c6d642f39d397a1a8f875d622022-12-21T20:24:53ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51391820-74212009-01-01748-991792610.2298/JSC0909917K0352-51390909917KSynthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dyeKurtoglu Nurcan0Kahramanmaraş Sütçü İmam University, Department of Textile Engineering, Avşar campus, Kahramanmaraş, TurkeyNew Ni(II), Cu(II) and Co(II) complexes were synthesized with the bidentate azo-azomethine dye, 4-[(E)-phenyldiazenyl]-2-[(E)-(phenylimino)methyl] phenol (dmpH), which was prepared by the reaction of 2-hydroxy-5-[(E)- phenyldiazenyl]benzaldehyde with aniline in EtOH. The syntheses of the metal chelates of the azo-azomethine dye were realized by the precipitation technique. The synthesized metal complexes were characterized by elemental analysis, molar conductance measurements, as well as infrared and UV-Vis spectral data. Based on these characterizations, the metal complexes of the transition metal ions may be formulated as [M(dmp)Cl(H2O)] where M = Ni(II), Cu(II) and Co(II). The metal complexes were formed by the coordination of N and O atoms of the ligand. The molar conductance values of the Ni(II), Cu(II) and Co(II) complexes of the bidentate ligand indicate their non-ionic character. The free ligand and its metal complexes were tested for their in vitro antimicrobial properties against eight bacteria: Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Mycobacterium smegmatis, Pseudomonas aeruginosa, Enterococcus cloacae, Bacillus megaterium, and Micrococcus luteus, and three fungi, Kluyveromyces fragilis, Rhodotorula rubra and Saccharomyces cerevisiae, in order to assess their antimicrobial potential. The [Ni(dmp)Cl(H2O)] chelate exhibited high activity against all the bacteria and fungi, except Rhodotorula rubra.http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909917K.pdfazo dyeazo-azomethinetransition metalsspectroscopyantimicrobial activity
spellingShingle Kurtoglu Nurcan
Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
Journal of the Serbian Chemical Society
azo dye
azo-azomethine
transition metals
spectroscopy
antimicrobial activity
title Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
title_full Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
title_fullStr Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
title_full_unstemmed Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
title_short Synthesis, characterization, chelation with transition metal ions, and antibacterial and antifungal studies of the 4-[(E)- -phenyldiazenyl]-2-[(E)-(phenylimino)methyl]phenol dye
title_sort synthesis characterization chelation with transition metal ions and antibacterial and antifungal studies of the 4 e phenyldiazenyl 2 e phenylimino methyl phenol dye
topic azo dye
azo-azomethine
transition metals
spectroscopy
antimicrobial activity
url http://www.doiserbia.nb.rs/img/doi/0352-5139/2009/0352-51390909917K.pdf
work_keys_str_mv AT kurtoglunurcan synthesischaracterizationchelationwithtransitionmetalionsandantibacterialandantifungalstudiesofthe4ephenyldiazenyl2ephenyliminomethylphenoldye