Synthesis, crystal structures, antimicrobial, antifungal and antituberculosis activities of mixed ligand silver(I) complexes

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dc.contributor.authorAltaf, Muhammad
dc.contributor.authorStoeckli-Evans, Helen
dc.contributor.authorCuin, Alexandre
dc.contributor.authorSato, Daisy Nakamura
dc.contributor.authorPavan, Fernando Rogério [UNESP]
dc.contributor.authorLeite, Clarice Queico Fujimura [UNESP]
dc.contributor.authorAhmad, Saeed
dc.contributor.authorBouakka, Mohammed
dc.contributor.authorMimouni, Mostafa
dc.contributor.authorKhardli, Fatima Zahra
dc.contributor.authorHadda, Taibi Ben
dc.contributor.institutionKing Fahd University of Petroleum and Minerals
dc.contributor.institutionUniversity of Neuchâtel
dc.contributor.institutionUniversidade Federal de Juiz de Fora (UFJF)
dc.contributor.institutionInstituto Adolfo Lutz (IAL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Engineering and Technology
dc.contributor.institutionFaculté des Sciences
dc.date.accessioned2014-05-27T11:30:51Z
dc.date.available2014-05-27T11:30:51Z
dc.date.issued2013-10-14
dc.description.abstractThe biological activity of some new mixed silver-phosphane-thio-ligand complexes, with 1:1:2, 1:1:1 and 1:2:1 (Ag:phospine:ligand) compositions, have been examined. Ten compounds were prepared using a series of silver(I) salts [AgX, where X = NO3, ClO4, PF6 and Br], tertiary phosphines and the ligands thi-osemicarbazide, 2-(propan-2-ylidene) hydrazinecarbothioamide, and thiazolidine-2-thione. The syntheses were carried out under ambient conditions, and the ten complexes obtained were found to be light stable. All 10 compounds were characterized by elemental analysis, FTIR, and NMR spectroscopy, whereas nine compounds were characterized by X-ray diffraction analysis. The anti-proliferative activities were evaluated by minimum inhibitory concentration (MIC: lg/mL) in an aqueous suspension system and they all show promising potential activity against selective strains of Gram-positive and Gram-negative bacteria, fungous and Mycrobaterium tuberculosis H37Rv. © 2013 Elsevier Ltd. All rights reserved.en
dc.description.affiliationDepartment of Chemistry King Fahd University of Petroleum and Minerals, 31261 Dhahran
dc.description.affiliationInstitute of Physics University of Neuchâtel, rue Emile-Argand 11, CH-2000 Neuchâtel
dc.description.affiliationDepartamento de Química Universidade Federal deJuiz de Fora (UFJF), Campus Universitário, Juiz de Fora, MG 36036-900
dc.description.affiliationLaboratório de Ribeirão Preto Instituto Adolfo Lutz, Ribeirão Preto, SP 14085-410
dc.description.affiliationDepartamento Ciências Biológicas Faculdade de Ciências Farmacêuticas UNESP, Araraquara, SP 14800-900
dc.description.affiliationDepartment of Chemistry University of Engineering and Technology, Lahore
dc.description.affiliationLaboratoire de Biochimie Faculté des Sciences, Oujda 6000
dc.description.affiliationLaboratoire de Chimie des Matériaux Faculté des Sciences, Oujda 60000
dc.description.affiliationUnespDepartamento Ciências Biológicas Faculdade de Ciências Farmacêuticas UNESP, Araraquara, SP 14800-900
dc.description.sponsorshipSwiss National Science Foundation
dc.format.extent138-147
dc.identifierhttp://dx.doi.org/10.1016/j.poly.2013.06.021
dc.identifier.citationPolyhedron, v. 62, p. 138-147.
dc.identifier.doi10.1016/j.poly.2013.06.021
dc.identifier.issn0277-5387
dc.identifier.lattes2114570774349859
dc.identifier.scopus2-s2.0-84885104441
dc.identifier.urihttp://hdl.handle.net/11449/76836
dc.identifier.wosWOS:000324226200018
dc.language.isoeng
dc.relation.ispartofPolyhedron
dc.relation.ispartofjcr2.067
dc.relation.ispartofsjr0,472
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectAnti-bacterial
dc.subjectAnti-tubercular
dc.subjectAntifungal
dc.subjectCrystal structure
dc.subjectSilver(I) complexes
dc.titleSynthesis, crystal structures, antimicrobial, antifungal and antituberculosis activities of mixed ligand silver(I) complexesen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
unesp.author.lattes2114570774349859
unesp.author.orcid0000-0003-2047-4142[1]
unesp.author.orcid0000-0002-6969-3963[5]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquarapt

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