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dc.contributor.authorSantamaría, David
dc.contributor.authorCano Sierra, Jesús 
dc.contributor.authorRoyo Gracia, Pascual 
dc.contributor.authorGonzález Mosquera, Marta Elena 
dc.contributor.authorCuenca Agreda, Tomás
dc.contributor.authorFrutos Gaite, Luis Manuel 
dc.date.accessioned2009-10-05T10:46:15Z
dc.date.available2009-10-05T10:46:15Z
dc.date.issued2005
dc.identifier.bibliographicCitationAngewandte Chemie, 2005, v. 44, p. 5828-5830en
dc.identifier.issn1521-3757
dc.identifier.urihttp://hdl.handle.net/10017/4197
dc.description.abstractA great deal of interest has focused on the role of metal ions as the active centers in the fixation of CO2 and its transformation. Activation of CO2 by hydroxo and oxo metal complexes to afford metal hydrogencarbonato and carbonato species, respectively, is related to the function of the carbonic anhydrase metalloenzyme, which catalyzes the physiologically important hydration of CO2 to hydrogencarbonate.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherJohn Wiley & Sonsen
dc.rights© Wiley, 2005en
dc.subjectSiliconen
dc.subjectTitaniumen
dc.subjectAb initio calculationsen
dc.subjectCarbon dioxide fixationen
dc.titleCarbon dioxide activation assisted by a bis(chlorodimethylsilyl)cyclopentadienyl titanium compounden
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaCIENCIAes_ES
dc.subject.ecienciaQuímica inorgánicaes_ES
dc.subject.ecienciaSCIENCEen
dc.subject.ecienciaChemistry, inorganicen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Química Inorgánica
dc.relation.publisherversionhttp://dx.doi.org/10.1002/ange.200500716
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1002/ange.200500716
dc.relation.projectIDMAT2004-02614 (Ministerio de Educación y Ciencia)
dc.relation.projectIDBQU2003-07281 (Ministerio de Ciencia y Tecnología)
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen


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