Synthesis, spectroscopic characterization and biocidal activity of some diorganotin(IV) complexes of salicylaldehydethiosemicarbazones and related ligands. Molecular and supramolecular structures of [R₂Sn(OArCHNNCSNH₂)], where R = Me, Ph and Ar =  C₆H₄, C₆H₃(5‐Br) and C₆H₃(5‐Cl), and of [Me₂Sn{OC₆H₃(5‐Br)CHNNCSNH₂}]·OH₂

Synthesis, Characterization, and Structure of Some Silicon Containing Diorganotin(IV) Complexes of Salicylaldehyde Thiosemicarbazones

“…13 C NMR signals for each carbon atom appear at their usual positions and compare well with the reported values. 11,12 The 119 Sn chemical shift values in compounds 1-4 are found to be in the range of -107.6 to -111.7 ppm. The appearance of chemical shift values in this region indicates five-coordination environment around the central tin atoms in compound 1-4.…”

{1-[(2-Oxidonaphthalen-1-yl)methylidene]thiosemicarbazidato-κ3N1,O,S}diphenyltin(IV)

“…For related organotin(IV) complexes with salicylaldehydethiosemicarbazones, see: Sarma et al (2007).…”

Synthesis, characterization, and antibacterial activity of triorganotin(IV) complexes of 2-methylphenol

“…In this context, systematic efforts have been made for the synthesis of new organotin complexes by choosing appropriate ligands. A variety of biologically potent ligands, amino acids [16], dipeptides [17,18], Schiff bases [19], and dithiocarbamates [20], have been used for the synthesis of organotin complexes. Only a few scattered reports are available on the synthesis of organotin complexes of phenols [21,22], despite the fact that phenolic ligands display great potential for tuning both steric and electronic influences.…”