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J Inorg Biochem ; 102(2): 285-92, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17976730

ABSTRACT

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.


Subject(s)
Anti-Bacterial Agents , Bacteria/drug effects , Nickel/chemistry , Organometallic Compounds , Sulfapyridine , Sulfisoxazole , Sulfonamides , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Crystallography, X-Ray , Escherichia coli/drug effects , Mycobacterium tuberculosis/drug effects , Organometallic Compounds/chemical synthesis , Organometallic Compounds/chemistry , Organometallic Compounds/pharmacology , Staphylococcus aureus/drug effects , Sulfapyridine/chemical synthesis , Sulfapyridine/chemistry , Sulfapyridine/pharmacology , Sulfisoxazole/chemical synthesis , Sulfisoxazole/chemistry , Sulfisoxazole/pharmacology , Sulfonamides/chemical synthesis , Sulfonamides/chemistry , Sulfonamides/pharmacology
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