Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/8246
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dc.contributor.authorJustino, Licínia L. G.-
dc.contributor.authorRamos, M. Luísa-
dc.contributor.authorCaldeira, M. Madalena-
dc.contributor.authorGil, Victor M. S.-
dc.date.accessioned2009-02-09T14:31:58Z-
dc.date.available2009-02-09T14:31:58Z-
dc.date.issued2000en_US
dc.identifier.citationEuropean Journal of Inorganic Chemistry. 2000:7 (2000) 1617-1621en_US
dc.identifier.urihttps://hdl.handle.net/10316/8246-
dc.description.abstractA multinuclear (1H, 13C, 17O, 51V) 1D and 2D NMR study of the complexation of l-lactic acid with vanadium(V) and hydrogen peroxide shows that four peroxo complexes are formed in aqueous solution in the pH range 1-7. Two isomeric 2:2:1 (metal:ligand:peroxo) complexes, together with a 2:2:2 species, are found over the entire pH range. At pH values below 2 an additional 1:1:1 complex is formed. The acid was found in all cases to act as a bidentate ligand through the carboxylic and the adjacent hydroxyl groups. To the best of our knowledge, this is the first report of dinuclear peroxovanadium complexes in which one of the metal centres is an oxovanadium centre (2:2:1 species).en_US
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titlePeroxovanadium(V) Complexes of L-Lactic Acid as Studied by NMR Spectroscopyen_US
dc.typearticleen_US
dc.identifier.doi10.1002/1099-0682(200007)2000:7<1617::AID-EJIC1617>3.0.CO;2-Ben_US
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-8338-6441-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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