Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20836
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dc.contributor.authorSegura, Daniel F.pt
dc.contributor.authorNetto, Adelino V. G.pt
dc.contributor.authorFrem, Regina C. G.pt
dc.contributor.authorMauro, Antonio E.pt
dc.contributor.authorSilva, Patricia B. dapt
dc.contributor.authorFernandes, José A.pt
dc.contributor.authorAlmeida Paz, Filipe A.pt
dc.contributor.authorDias, Amanda L. T.pt
dc.contributor.authorSilva, Naiara C.pt
dc.contributor.authorAlmeida, Eduardo T. dept
dc.contributor.authorMarques, Marcos J.pt
dc.contributor.authorAlmeida, Letícia dept
dc.contributor.authorAlves, Karina F.pt
dc.contributor.authorPavan, Fernando R.pt
dc.contributor.authorSouza, Paula C. dept
dc.contributor.authorBarros, Heloisa B. dept
dc.contributor.authorLeite, Clarice Q. F.pt
dc.date.accessioned2017-12-07T20:01:09Z-
dc.date.issued2014pt
dc.identifier.issn0277-5387pt
dc.identifier.urihttp://hdl.handle.net/10773/20836-
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.pt
dc.language.isoengpt
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F63736%2F2009/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132936/PTpt
dc.rightsrestrictedAccesspor
dc.subjectANTIMICROBIAL ACTIVITIESpt
dc.subjectCRYSTAL-STRUCTURESpt
dc.subjectIN-VITROpt
dc.subjectSPECTROSCOPIC CHARACTERIZATIONpt
dc.subjectTRIPHENYLPHOSPHINE LIGANDSpt
dc.subjectMYCOBACTERIUM-TUBERCULOSISpt
dc.subjectANTIMYCOBACTERIAL ACTIVITYpt
dc.subjectLEISHMANICIDAL ACTIVITYpt
dc.subjectSUBSTITUTED THIOUREASpt
dc.subjectCOORDINATION POLYMERSpt
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)pt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage197pt
degois.publication.lastPage206pt
degois.publication.titlePOLYHEDRONpt
degois.publication.volume79pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1016/j.poly.2014.05.004pt
dc.identifier.doi10.1016/j.poly.2014.05.004pt
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