Synthesis and characterization of two new hydroxamic acids derivatives and their metal complexes. An investigation on the keto/enol, E/Z and hydroxamate/hydroximate forms

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2-phenylbenzimidazole-N-acetohydroxamic acid (HL1), 2-phenylbenzimidazole-N-butanohydroxamic acid (HL2) and Ni(II), Cu(II), Zn(II) and Cd(II) metal complexes have been synthesized and characterized by elemental analyses, 1H NMR, 13C NMR, FT-IR spectrometry, LC-MS (ESI+) and thermal analyses. The results of NMR spectra and theoretical calculations showed that the hydroxamic acids were in the keto-E and keto-Z conformations. The elemental analysis and thermal analysis indicated that M:L ratio of the complexes are 1:1 and the spectral analysis confirmed that hydroxamate groups are keto form in the Ni(II) and Zn(II) complexes of 2-phenylbenzimidazole-N-butanohydroxamic acid and enol form in the other complexes. © 2016 Elsevier B.V.

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AlanDeğerDil
dc.contributor.authorAdiguzel, Ekrem
dc.contributor.authorYilmaz, Fatih
dc.contributor.authorEmirik, Mustafa
dc.contributor.authorOzil, Musa
dc.date.accessioned2026-10-18T20:29:45.626833080Z
dc.date.available2026-10-18T20:29:45.626833080Z
dc.date.issued2017
dc.description.abstract2-phenylbenzimidazole-N-acetohydroxamic acid (HL1), 2-phenylbenzimidazole-N-butanohydroxamic acid (HL2) and Ni(II), Cu(II), Zn(II) and Cd(II) metal complexes have been synthesized and characterized by elemental analyses, 1H NMR, 13C NMR, FT-IR spectrometry, LC-MS (ESI+) and thermal analyses. The results of NMR spectra and theoretical calculations showed that the hydroxamic acids were in the keto-E and keto-Z conformations. The elemental analysis and thermal analysis indicated that M:L ratio of the complexes are 1:1 and the spectral analysis confirmed that hydroxamate groups are keto form in the Ni(II) and Zn(II) complexes of 2-phenylbenzimidazole-N-butanohydroxamic acid and enol form in the other complexes. © 2016 Elsevier B.V.
dc.description.sponsorshipThis work was supported by Research Fund of the Recep Tayyip Erdogan University , Project Number: BAP-2013.102.02.4 . The theoretical calculations reported in this paper were fully performed at TUBITAK ULAKBIM, High Performance and Grid Computing Center (TRUBA resources).
dc.identifier.doi10.1016/j.molstruc.2016.07.081
dc.identifier.eissn1872-8014
dc.identifier.endpage412
dc.identifier.issn0022-2860
dc.identifier.scopus2-s2.0-84982860534
dc.identifier.startpage403
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/14958
dc.identifier.volume1127
dc.identifier.wosWOS:000385901800048
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Molecular Structure
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBenzimidazole
dc.subjectConformer
dc.subjectHydroxamic acid
dc.subjectHydroximate
dc.subjectMetal complexes
dc.subjectTautomer
dc.subjectTheoretical calculation
dc.subjectCadmium
dc.subjectChemical analysis
dc.subjectComplexation
dc.subjectCopper
dc.subjectMetal analysis
dc.subjectNickel
dc.subjectNuclear magnetic resonance spectroscopy
dc.subjectOrganic acids
dc.subjectPolymethyl methacrylates
dc.subjectSpectrum analysis
dc.subjectThermoanalysis
dc.subjectZinc
dc.subjectZinc compounds
dc.subjectBenzimidazoles
dc.subjectHydroxamic acids
dc.subjectTheoretical calculations
dc.subjectSynthesis (chemical)
dc.titleSynthesis and characterization of two new hydroxamic acids derivatives and their metal complexes. An investigation on the keto/enol, E/Z and hydroxamate/hydroximate forms
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus48
rdl.citation.wos42
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)