Synthesis, Characterization and in vitro antimicrobial activity of dialkyltin(IV)bis(fusidate) complexes.
- Autori: FIORE T; ABBATE M; CASELLA G; CATALDO S; NAGY L; PELLERITO C; PRINZIVALLI C; SCHILLACI D; SCOPELLITI M; PELLERITO L
- Anno di pubblicazione: 2008
- Tipologia: Articolo in rivista (Articolo in rivista)
- Parole Chiave: Dialkyltin(IV), FT-IR, Mössbauer, NMR, antimicrobial tests
- OA Link: http://hdl.handle.net/10447/35138
Abstract
The complexation of one steroid antibiotic of the fusidane family, sodium fusidate [sodium 2-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12, 13,15,16-dodeca hydro-1H-cyclopenta[a]phenanthren-7-ylidene)-6-methyl-hept-5-enoate = (Nafus)], by dialkyltin(IV) has been studied by conventional technique as FT-IR, Mössbauer and NMR spectroscopies. Analytical data supported the general formula Alk2Sn(IV)fus2 (Alk = Me, Bu). Infrared spectral data of the complexes imply the presence of both uni- and bidentate, ester-type and bridging carboxylate group, respectively. On the basis of FT-IR and 119Sn Mössbauer spectroscopy, in both Me2Sn(IV)fus2 and Bu2Sn(IV)fus2, trigonal bipyramidal configurations are proposed. NMR spectra, of both ligand and of the complexes were carried in DMSO-d6 solution, in which dialkyltin(IV)bis(fusidate) maintained their solid-state configuration. In vitro antimicrobial tests were performed on complexes, and good anti-staphylococcal activity was observed.