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Synthesis and biological evaluation of ternary silver compounds bearing N,N-chelating ligands and thiourea: X-ray structure of [{Ag(bpy) (mu-tu)}(2)](NO3)(2) (bpy=2,2 '-bipyridine; tu = thiourea)

dc.contributor.authorSegura, Daniel F. [UNESP]
dc.contributor.authorNetto, Adelino Vieira de Godoy [UNESP]
dc.contributor.authorFrem, Regina Célia Galvão [UNESP]
dc.contributor.authorMauro, Antonio Eduardo [UNESP]
dc.contributor.authorSilva, Patricia B. da [UNESP]
dc.contributor.authorFernandes, Jose A.
dc.contributor.authorPaz, Filipe A. A.
dc.contributor.authorDias, Amanda L. T.
dc.contributor.authorSilva, Naiara C.
dc.contributor.authorAlmeida, Eduardo T. de
dc.contributor.authorMarques, Marcos J.
dc.contributor.authorAlmeida, Leticia de
dc.contributor.authorAlves, Karina F.
dc.contributor.authorPavan, Fernando R. [UNESP]
dc.contributor.authorSouza, Paula C. de [UNESP]
dc.contributor.authorBarros, Heloisa B. de [UNESP]
dc.contributor.authorLeite, Clarice Q. F. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv Aveiro
dc.contributor.institutionUniv Fed Alfenas
dc.date.accessioned2015-03-18T15:53:59Z
dc.date.available2015-03-18T15:53:59Z
dc.date.issued2014-09-05
dc.description.abstractCompounds [{Ag(phen)(mu-tu)}(2)](NO3)(2) (1), [{Ag(phen)(mu-tu)}(2)](CF3SO3)(2) (2), [{Ag(bpy)(mu-tu)}(2)](NO3)(2) (3) (where phen = 1,10-phenanthroline; bpy = 2,2'-bipyridine; tu = thiourea) were prepared by reacting the appropriate AgX salt (X- = NO3-, CF3SO3-), the N,N-chelating ligand (phen or bpy) and thiourea in a ca. 1:1:2 M ratio, respectively. The silver(l) complexes were characterized by elemental analysis, infrared (IR), H-1 and C-13 NMR spectroscopies, MS/ESI and conductivity measurements. The IR and NMR data were consistent with the presence of chelating phen (1 and 2) and bpy (3) ligands and demonstrated the S-coordination mode of thiourea. The crystal and molecular structures of compound [{Ag(bpy)(mu-tu)}(2)] (NO3)(2) (3) were determined by single-crystal X-ray diffraction. The complexes 1-3 were screened for their in vitro antimycobacterial (Mycobacterium tuberculosis), antileishmanial (Leishmania (L) amazonensis), antibacterial (Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa), antifungal activities (Candida albi cans, Candida tropicalis, Candida krusei). (C) 2014 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUNESP, Inst Quim Araraquara, Dept Quim Geral & Inorgan, BR-14801970 Araraquara, SP, Brazil
dc.description.affiliationUniv Aveiro, CICECO, Dept Chem, P-3810193 Aveiro, Portugal
dc.description.affiliationUniv Fed Alfenas, UNIFAL MG, BR-37130000 Alfenas, MG, Brazil
dc.description.affiliationUNESP, Fac Ciencias Farmaceut Araraquara, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Quim Araraquara, Dept Quim Geral & Inorgan, BR-14801970 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Ciencias Farmaceut Araraquara, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipFundacao para a Ciencia e a Tecnologia (FCT, Portugal)
dc.description.sponsorshipFEDER (Portugal)
dc.description.sponsorshipCOMPETE
dc.description.sponsorshipIdCNPq: 487092/2012-0
dc.description.sponsorshipIdCOMPETESFRH/BPD/63736/2009
dc.description.sponsorshipIdCOMPETEPTDC/QUI-QUI/098098/2088 (FCOMP-01-0124-FEDER-010785)
dc.format.extent197-206
dc.identifierhttp://dx.doi.org/10.1016/j.poly.2014.05.004
dc.identifier.citationPolyhedron. Oxford: Pergamon-elsevier Science Ltd, v. 79, p. 197-206, 2014.
dc.identifier.doi10.1016/j.poly.2014.05.004
dc.identifier.issn0277-5387
dc.identifier.lattes3300223970814448
dc.identifier.lattes7927677053650819
dc.identifier.orcid0000-0002-0057-7964
dc.identifier.urihttp://hdl.handle.net/11449/116714
dc.identifier.wosWOS:000340313800023
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPolyhedron
dc.relation.ispartofjcr2.067
dc.relation.ispartofsjr0,472
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectSilver(I)en
dc.subject1,10-Phenanthrolineen
dc.subjectAntileishmanial activityen
dc.subjectTuberculosisen
dc.subjectAntifungal and antibacterial activityen
dc.titleSynthesis and biological evaluation of ternary silver compounds bearing N,N-chelating ligands and thiourea: X-ray structure of [{Ag(bpy) (mu-tu)}(2)](NO3)(2) (bpy=2,2 '-bipyridine; tu = thiourea)en
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes3300223970814448[4]
unesp.author.lattes7927677053650819[2]
unesp.author.orcid0000-0002-0057-7964[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentQuímica Inorgânica - IQARpt

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