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J Inorg Biochem ; 102(2): 285-92, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17976730

RESUMO

The synthesis, structural characterization, voltammetric experiments and antibacterial activity of [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] were studied and compared with similar previously reported copper complexes. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O crystallized in a monoclinic system, space group C2/c where the nickel ion was in a slightly distorted octahedral environment, coordinated with two sulfisoxazole molecules through the heterocyclic nitrogen and four water molecules. [Ni(sulfapyridine)(2)] crystallized in a orthorhombic crystal system, space group Pnab. The nickel ion was in a distorted octahedral environment, coordinated by two aryl amine N from two sulfonamides acting as monodentate ligands and four N atoms (two sulfonamidic N and two heterocyclic N) from two different sulfonamide molecules acting as bidentate ligands. Differential pulse voltammograms were recorded showing irreversible peaks at 1040 and 1070 mV, respectively, attributed to Ni(II)/Ni(III) process. [Ni(sulfisoxazole)(2)(H(2)O)(4)].2H(2)O and [Ni(sulfapyridine)(2)] presented different antibacterial behavior against Staphylococcus aureus and Escherichia coli from the similar copper complexes and they were inactive against Mycobacterium tuberculosis.


Assuntos
Antibacterianos , Bactérias/efeitos dos fármacos , Níquel/química , Compostos Organometálicos , Sulfapiridina , Sulfisoxazol , Sulfonamidas , Antibacterianos/síntese química , Antibacterianos/química , Antibacterianos/farmacologia , Cristalografia por Raios X , Escherichia coli/efeitos dos fármacos , Mycobacterium tuberculosis/efeitos dos fármacos , Compostos Organometálicos/síntese química , Compostos Organometálicos/química , Compostos Organometálicos/farmacologia , Staphylococcus aureus/efeitos dos fármacos , Sulfapiridina/síntese química , Sulfapiridina/química , Sulfapiridina/farmacologia , Sulfisoxazol/síntese química , Sulfisoxazol/química , Sulfisoxazol/farmacologia , Sulfonamidas/síntese química , Sulfonamidas/química , Sulfonamidas/farmacologia
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