Abstract
Reaction of n-butyltin trichloride, [BunSnCl3], and phenyltin trichloride, [PhSnCl3], with 2-acetylpyridine benzoyl hydrazone (H2AcPh), 2-acetylpyridine para-chloro-benzoyl hydrazone (H2AcpClPh) and 2-acetylpyridine para-nitro-benzoyl hydrazone (H2AcpNO2Ph) gave [BunSn(2AcPh)Cl2] (1), [BunSn(2AcpClPh)Cl 2] (2), [BunSn(2AcpNO2Ph)Cl2] (3), [PhSn(2AcPh)Cl2] (4), [PhSn(2AcpClPh)Cl2] (5) and [PhSn(2AcpNO2Ph)Cl2] (6) as products. Among the hydrazones H2AcpClPh proved to be the most active against Staphylococcus aureus and Candida albicans. Upon coordination the antibacterial activity of both tin and the hydrazones significantly increases. Complexes 2 and 5 revealed to be the most active as antimicrobial agents.
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Despaigne, A. A. R., Vieira, L. F., Mendes, I. C., Da Costa, F. B., Speziali, N. L., & Beraldo, H. (2010). Organotin(IV) Complexes with 2-acetylpyridine benzoyl hydrazones: Antimicrobial activity. Journal of the Brazilian Chemical Society, 21(7), 1247–1257. https://doi.org/10.1590/S0103-50532010000700012
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