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


Alyar H., Alyar S., ÜNAL A., Özbek N., ŞAHİN E., KARACAN N.

Journal of Molecular Structure, vol.1028, pp.116-125, 2012 (SCI-Expanded, Scopus) identifier

  • Publication Type: Article / Article
  • Volume: 1028
  • Publication Date: 2012
  • Doi Number: 10.1016/j.molstruc.2012.06.046
  • Journal Name: Journal of Molecular Structure
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.116-125
  • Keywords: Antibacterial activity, DFT, Disulfonamides, FT-IR and Raman, SQM-FF, X-ray
  • Bilecik Şeyh Edebali University Affiliated: Yes

Abstract

M-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, 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. © 2012 Elsevier B.V. All rights reserved.