Utilize este identificador para referenciar este registo: http://hdl.handle.net/1822/22477

TítuloNickel(II) complexes of N′-(2-thienylcarbonyl)thiocarbamates O-alkyl-esters : structural and spectroscopic characterization and evaluation of their microbiological activities
Autor(es)Gomes, Gomes, Lígia Rebelo
Low, John Nicolson
Rocha, Marisa A. A.
Santos, Luís M. N. B. F.
Schröder, Bernd
Brandão, Paula
Matos, Carla Maria
Neves, J. M.
Palavras-chaveMedicinal plants
Ethnobotany
NE Portugal
Folk medicine
Thiocarbamates O-alkyl-esters
Ni(II) complexes
Rx
Spectroscopic characterization
Antimicrobial activity
Data2011
EditoraElsevier
RevistaJournal of Molecular Structure
Resumo(s)In the present work a set of five Ni(II) complexes with general formula [Ni(L)2] and with HL = N-thenoylthiocarbamic-O-n-alkylylesters (n = 2–6) has been prepared and characterized in solution by UV–vis and NMR spectroscopies. Three of them were also characterized in the solid state by X-ray diffractometry. The energy rotation of the thiophene ring of ligand was evaluated theoretically. Liposomes of complexes were prepared in order to evaluate their ability to interact with the membrane. Furthermore, their biological activities were evaluated in a set of bacteria (gram+ and gram−) and yeasts. The X-ray structure determination confirms that bidentate ligand forms a tetra co-ordinated complex with an S2O2 co-ordination sphere around the nickel(II) ion in a cis configuration. The metal centre is coordinated in a square planar fashion. NMR spectra taken in solution show a diamagnetic signal compatible with a square-planar geometry around the metal centre. The values obtained for the liposome/water partition coefficients (Kp) show that [Ni(ttete)2] and [Ni(ttpre)2] have a similar membrane partition ability, whilst the [Ni(ttbue)2] derivative presents a significantly higher Kp, describing a stronger interaction within the membrane. For all the compounds, [Ni(ttpre)2] has a higher efficacy against Gram negative bacteria and yeasts nevertheless, the anti-yeast and anti-bacterial activity values of all tested compounds are lower than ones of the reference compounds.
Tipoarticle
URIhttp://hdl.handle.net/1822/22477
DOI10.1016/j.molstruc.2011.01.021
ISSN0022-2860
Versão da editorahttp://www.journals.elsevier.com/
Arbitragem científicayes
AcessorestrictedAccess
Aparece nas coleções:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
1-s2.0-S0022286011000536-main.pdf1 MBAdobe PDFVer/Abrir  Solicitar cópia ao autor!

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu Currículo DeGóis