Abstract
A series of organotin(IV) complexes have been synthesized by reacting potassium o-isobutyl carbonodithioate with di- and triorganotin halides in methanol under stirring conditions. The newly synthesized complexes have been characterized by elemental analysis, FT-IR, NMR (1H and 13C) and X-ray crystallography. The FT-IR results show that the ligand acts as bidentate in complexes 1–3 and monodentate in complexes 4 and 5, which were also confirmed by theoretical calculations. The NMR data reveal four and six coordinated geometries in solution. A HOMO–LUMO study shows that all the complexes are stable. Biological screenings demonstrate that, with a few exceptions, all the complexes show significant activity against various bacterial and fungal strains. The synthesized complexes were also found to be effective antioxidants of the 2,2-diphenyl-1-picrylhydrazyl radical (DPPH). All the complexes have been assayed for antileishmanial activity in vitro and found some promising results. The UV–Vis studies confirmed that the ligand and its complexes bind to DNA via intercalative interactions, resulting in hypochromism and minor red shifts.
Published Version
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