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Synthesis, Characterization, Biocide and Toxicological Activities of Di-N-Butyl- And diphenyl-tin(IV)-salicyliden-beta-amino Alcohol Derivatives

Luis S Zamudio-Rivera, Rocio George-Tellez, Gerson López-Mendoza, Adela Morales-Pacheco, Eugenio Flores, Herbert Höpfl, Victor Barba, Francisco J Fernández, Nathalie Cabirol, Hiram I Beltrán

Inorg Chem. 2005 Jul 25;44(15):5370-8.

PMID: 16022535

Abstract:

The one pot reaction of salicylaldehyde 1, beta-amino alcohols 2a-2c, and di-n-butyltin(IV) oxide 3a or diphenyltin(IV) oxide 3b produced five diorganotin(IV) compounds, 4a-4c, 5a, and 5c, in good yields. All compounds were characterized by IR, (1)H, (13)C, and (119)Sn NMR spectroscopy, and elemental analysis; furthermore, compounds 4b, 4c, 5a, and 5c were characterized by X-ray diffraction analysis. After the structural characterization, all of the compounds were tested in vitro against Bacillus subtilis (Gram-positive, strain ATCC 6633), Escherichia coli (Gram-negative, strain DH5alpha), Pseudomonas aeruginosa (Gram-negative, strain BH3), Desulfovibrio longus (strain DSM 6739), and Desulfomicrobium aspheronum (strain DSM 5918) to assess their antimicrobial activity. Compounds 4 and 5 demonstrated a wide range of bactericidal activities against the tested aerobic (one Gram-positive and two Gram-negative subtypes) and anaerobic bacteria (two sulfate-reducing bacteria, SRB). Compound 5 had better bactericidal performances than compound 4. For all of the compounds, the acute toxicity was measured using luminescent bacteria toxicity (LBT-Microtox) tests to track their further environmental impact. According to these results and in order to fulfill environmental regulations, the toxicity of the compounds studied herein can be modulated through the proper selection of the disubstituted tin(IV) moiety.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP2273510 Diphenyltin(IV) oxide Diphenyltin(IV) oxide 2273-51-0 Price
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