Synthesis, characterization and antibacterial studies of N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide and its neodymium(III) and thallium(III) complexes

  • Lawrence Nnamdi Obasi
  • , Uchechukwu Susan Oruma
  • , Ibrahim Abdulrazak Al-Swaidan
  • , Ponnadurai Ramasami
  • , Chigozie Julius Ezeorah
  • , Alfred Ezinna Ochonogor

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

N-(Benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) was synthesized by condensation reaction of 4-chlorobenzenesulphonyl chloride and 2-aminobenzothiazole in acetone under reflux. Neodymium(III) and thallium(III) complexes of the ligand were also synthesized. Both ligand and metal complexes were characterized using UV-Vis, IR, 1H- and 13C-NMR spectroscopies, elemental analysis and molar conductance measurement. IR studies revealed that the ligand is tridentate and coordinates to the metal ions through nitrogen and oxygen atoms of the sulphonamide group and nitrogen atom attached to benzothiazole ring. The neodymium(III) complex displays a coordination number of eight while thallium(III) complex displays a coordination number of six. The ligand and its complexes were screened in vitro for their antibacterial activities against Escherichia coli strains (E. coli 6 and E. coli 13), Proteus species, Staphylococcus aureus and Pseudomonas aeruginosa using the agar well diffusion technique. The synthesized compounds were found to be more active against the microorganisms screened relative to ciprofloxacin, gentamicin and co-trimoxazole.

Original languageEnglish
Article number153
JournalMolecules
Volume22
Issue number2
DOIs
Publication statusPublished - Feb 2017

Keywords

  • Antibacterial activity
  • N-(benzothiazol-2-yl)-4-chlorobenzenesulphonamide
  • Neodymium(III) and thallium(III) complexes

ASJC Scopus subject areas

  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Pharmaceutical Science
  • Drug Discovery
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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