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Abstract
In vitro antibacterial activity of some organotin(IV) chlorobenzoates including diphenyltin(IV) o-, m-, p-dichlorobenzoate (2, 3, 4) and triphenyltin(IV) o-, m-, p-chlorobenzoate (6, 7, 8) against Staphylococcus aureus and Escherichia coli was studied. The compounds were synthesized by the reaction of diphenyltin(IV) dihydroxide (1) and triphenyltin(IV) hydroxide (5) with o-, m-, p-chlorobenzoic acid in a maximum refluxed time of 4 h using methanol as the solvent of the reaction. The antibacteri
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