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The goal of this research work is to create a new class of diorganotin(IV) complexes with general formula R 2 SnL 1-4 , where R = CH 3 , C 2 H 5 , C 4 H 9  &amp; C 6 H 5 , and L 1-4  are the Schiff base ligands derived from the condensation of indole-3-acetic acid hydrazide with salicylaldehyde derivatives in 1:1 molar ratio. Various spectral (FTIR, NMR and mass spectrometry) and physico-chemical (XRD, TGA) techniques were utilized to identify the structure of the prepared compounds. Spectroscopic evidence suggests that Schiff base ligands coordinate to the central tin atom in a tridentate manner with ONO as the donor site, thus forming a pentacoordinate environment around the metal ion. The serial dilution method was employed for carrying out the antimicrobial activity of the produced compounds against four bacterial strains and two fungal strains. The observed results of biocidal activity showed that compounds Ph 2 SnL 3  ( 16 ) and Ph 2 SnL 4  ( 20 ) were found to be most potent against the tested strains. Further, molecular docking studies for active compounds i.e.,  16  and  20  were carried out in the active site of  Escherichia coli  3-oxoacyl-[acyl-carrier-protein] synthase 2 (FabF). To check the drug-likeness,  in silico  studies of the synthesized compounds was carried out and it has been found that compounds can be used as orally active drugs.

Organotin(IV) complexes derived from hydrazone ligands: Synthesis, spectral analysis, antimicrobial and molecular docking studies