Synthesis, characterization and antimicrobial activity of m-toluenesulfonamide, N,Na2-1,2-ethanediylbis (mtsen) and [Cu(II)(phenanthroline)2]mtsen complex

M-toluenesulfonamide, N,Na2-1,2-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, Four...

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Veröffentlicht in:Journal of molecular structure 2012-11, Vol.1028, p.116-125
Hauptverfasser: Alyar, Hamit, Alyar, Saliha, Uenal, Arslan, Oezbek, Neslihan, Sahin, Ertan, Karacan, Nurcan
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Sprache:eng
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Zusammenfassung:M-toluenesulfonamide, N,Na2-1,2-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, 1H, 13C, 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, 1H and 13C NMR analyses were performed at B3LYP/6-311++G(d,p) theory level using gauge including atomic orbital (GIAO) 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.
ISSN:0022-2860
DOI:10.1016/j.molstruc.2012.06.046