Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20595
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dc.contributor.authorda Silva, Cristianapt
dc.contributor.authorRibeiro, Leonardo B.pt
dc.contributor.authorFuruno, Caio C.pt
dc.contributor.authorda Cunha, Gislaine A.pt
dc.contributor.authorde Souza, Ronan F. F.pt
dc.contributor.authorNetto, Adelino V. G.pt
dc.contributor.authorMauro, Antonio E.pt
dc.contributor.authorFrem, Regina C. G.pt
dc.contributor.authorFernandes, Jose A.pt
dc.contributor.authorAlmeida Paz, Filipe A.pt
dc.contributor.authorMarino, Leonardo B.pt
dc.contributor.authorPavan, Fernando R.pt
dc.contributor.authorLeite, Clarice Q. F.pt
dc.date.accessioned2017-12-07T19:52:43Z-
dc.date.issued2015pt
dc.identifier.issn0277-5387pt
dc.identifier.urihttp://hdl.handle.net/10773/20595-
dc.description.abstractComplexes of the type trans-[PdCl2(HL)(PPh3)], where HL = pyrazole (1); 3,5-dimethylpyrazole (2); 4-nitropyrazole (3); 4-iodopyrazole (4) and PPh3 = triphenylphosphine, were synthesized and characterized by elemental analyses, infrared and H-1 NMR spectroscopies. Single-crystal X-ray diffraction determination on 3.0.9 CHCl3 and 4 showed that the coordination geometry around Pd(II) is nearly square-planar, with the chloro ligands in a trans configuration. In vitro antimycobacterial evaluation demonstrated that compound 4 displayed a minimum inhibitory concentration (MIC) of 7.61 +/- 2.18 mu M, being superior to the values observed for some commonly used antituberculosis drugs and other metal-based complexes. (C) 2015 Elsevier Ltd. All rights reserved.pt
dc.language.isoengpt
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F63736%2F2009/PTpt
dc.rightsrestrictedAccesspor
dc.subjectTUBERCULOSIS PANTOTHENATE SYNTHETASEpt
dc.subjectALAMAR BLUE ASSAYpt
dc.subjectMYCOBACTERIUM-TUBERCULOSISpt
dc.subjectPALLADIUM(II) COMPLEXESpt
dc.subjectBIOLOGICAL EVALUATIONpt
dc.subjectSTRUCTURAL-CHARACTERIZATIONpt
dc.subjectSUPRAMOLECULAR CHEMISTRYpt
dc.subjectN BONDpt
dc.subjectLIGANDSpt
dc.subjectINHIBITORSpt
dc.titlePyrazolyl Pd(II) complexes containing triphenylphosphine: Synthesis and antimycobacterial activitypt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage10pt
degois.publication.lastPage16pt
degois.publication.titlePOLYHEDRONpt
degois.publication.volume100pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1016/j.poly.2015.07.009pt
dc.identifier.doi10.1016/j.poly.2015.07.009pt
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