Synthesis, characterization and antimicrobial activity of m-toluenesulfonamide, N,N′-1,2-ethanediylbis (mtsen) and [Cu(II)(phenanthroline)2]mtsen complex

dc.authoridUnal, Arslan/0000-0002-5857-7318
dc.contributor.authorAlyar, Hamit
dc.contributor.authorAlyar, Saliha
dc.contributor.authorUnal, Arslan
dc.contributor.authorOzbek, Neslihan
dc.contributor.authorSahin, Ertan
dc.contributor.authorKaracan, Nurcan
dc.date.accessioned2025-05-20T18:58:07Z
dc.date.issued2012
dc.departmentBilecik Şeyh Edebali Üniversitesi
dc.description.abstractM-toluenesulfonamide, N,N'-1,2-ethanediylbis (a disulfonamide compound, mtsen) and [Cu(II)(phenanthroline)(2)]mtsen compounds were newly synthesized. The molecular structure of mtsen was investigated by using elemental analyses, liquid chromatography-mass spectrometry (LC-MS), X-ray diffraction, Fourier transform infrared spectroscopy (FT-IR), dispersive Raman spectroscopy, H-1, C-13, heteronuclear chemical-shift correlation (HETCOR) and correlation spectroscopy (COSY) NMR spectroscopies. The FT-IR, dispersive Raman and far-infrared spectra of mtsen were recorded at room-temperature and discussed assisted with B3LYP/6-311G(d,p) level of theory along with scaled quantum mechanics force field (SQM-FF) method. Furthermore, H-1 and C-13 NMR analyses were performed at B3LYP/6-311++G(d,p) theory level using gauge including atomic orbital (CIAO) method and compared with the experimental findings. Further analyses were also made for [Cu(II)(phenanthroline)(2)]mtsen complex by using elemental analysis, LC-MS, magnetic susceptibility; conductivity measurement and FT-IR. The antibacterial activities of synthesized compounds were studied against some Gram-positive and Gram-negative bacteria by using the microdilution and disk diffusion method. The biological activity screening showed that complex have more activity than ligand against the tested bacteria. (C) 2012 Elsevier B.V. All rights reserved.
dc.identifier.doi10.1016/j.molstruc.2012.06.046
dc.identifier.endpage125
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.scopus2-s2.0-84868253317
dc.identifier.scopusqualityQ1
dc.identifier.startpage116
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2012.06.046
dc.identifier.urihttps://hdl.handle.net/11552/8116
dc.identifier.volume1028
dc.identifier.wosWOS:000311174800018
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWoS
dc.indekslendigikaynakScopus
dc.indekslendigikaynakWoS - Science Citation Index Expanded
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Molecular Structure
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250518
dc.subjectDisulfonamides
dc.subjectX-ray
dc.subjectDFT
dc.subjectSQM-FF
dc.subjectFT-IR and Raman
dc.subjectAntibacterial activity
dc.titleSynthesis, characterization and antimicrobial activity of m-toluenesulfonamide, N,N′-1,2-ethanediylbis (mtsen) and [Cu(II)(phenanthroline)2]mtsen complex
dc.typeArticle

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