Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/6105
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dc.contributor.authorGirginova, Penka I.pt
dc.contributor.authorAlmeida Paz, Filipe A.pt
dc.contributor.authorNogueira, Helena I. S.pt
dc.contributor.authorSilva, Nuno J. O.pt
dc.contributor.authorAmaral, Vítor S.pt
dc.contributor.authorKlinowski, Jacekpt
dc.contributor.authorTrindade, Titopt
dc.date.accessioned2012-02-09T14:48:31Z-
dc.date.issued2005-03-
dc.identifier.issn0277-5387pt
dc.identifier.urihttp://hdl.handle.net/10773/6105-
dc.description.abstractTwo complexes with Co2+ and 3-hydroxypicolinic acid, [Co(picOH)2(H2O)2] (I) and mer-[N(CH3)4][Co(picOH)3] Æ H2O (II), have been synthesised and characterised using single-crystal X-ray diffraction, elemental analysis, infrared spectroscopy, and thermoanalytical measurements. The 3-hydroxypicolinate ligands are coordinated to the Co2+ centres via its typical N,O-chelating coordination fashion. While in I the presence of two coordinated water molecules leads to the formation of a neutral [Co(picOH)2(H2O)2] complex which is strongly hydrogen bonded to another four neighbouring complexes, in II the inclusion of a third picOH ligand leads to an anionic octahedral complex, [Co(picOH)3] , in which all the N- and O-atoms are occupying mer positions. The properties of these two compounds were further investigated by measuring their magnetic behaviour.pt
dc.language.isoengpt
dc.rightsrestrictedAccesspor
dc.subjectCobalt complexespt
dc.subjectCrystal structurespt
dc.subject3-Hydroxypicolinic acidpt
dc.subjectMagnetic propertiespt
dc.titleSynthesis, characterisation and magnetic properties of cobalt (II) complexes with 3-hydroxypicolinic acid (HpicOH): [Co(picOH)2(H2O)(2)] and mer-[N(CH3)(4)][Co(picOH)(3)] . H2Opt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage563pt
degois.publication.issue4pt
degois.publication.lastPage569pt
degois.publication.titlePolyhedronpt
degois.publication.volume24pt
dc.date.embargo10000-01-01-
dc.identifier.doi10.1016/j.poly.2005.01.002*
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