dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorMartin, Cibely S.
dc.creatorTeixeira, Marcos F. S.
dc.date2015-10-21T20:50:00Z
dc.date2016-10-25T21:08:54Z
dc.date2015-10-21T20:50:00Z
dc.date2016-10-25T21:08:54Z
dc.date2015-01-30
dc.date.accessioned2017-04-06T09:08:50Z
dc.date.available2017-04-06T09:08:50Z
dc.identifierInorganica Chimica Acta, v. 425, p. 76-82, 2015.
dc.identifier0020-1693
dc.identifierhttp://hdl.handle.net/11449/129319
dc.identifierhttp://acervodigital.unesp.br/handle/11449/129319
dc.identifierhttp://dx.doi.org/10.1016/j.ica.2014.10.009
dc.identifierWOS:000345755700011
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/939874
dc.descriptionMany high-valence multinuclear mu-oxo-bridged manganese complexes have been synthesized to mimic the active site of the natural enzymes. The electrochemical and kinetic parameters were determined for two mimicking complexes ([(Mn2O2)-O-IV(terpy)(2)(H2O)(2)](4+) and [(Mn4O5)-O-IV(terpy)(4)(H2O)(2)](6+)) by cyclic voltammetry and linear sweep voltammetry using a rotating disk electrode (RDE). Stability and kinetic behavior are directly related to mu-oxo bridges, where the mu-oxo-bridge provides a fast electron transition between metal centers due to stabilization of dx(2) - y(2) orbitals by the oxygen bond. On the other hand, when the dx(2) - y(2) orbitals are stabilized by aqua ligands by a coordination bond, a displacement of oxidation potential to more positive potential was observed. A shift of the potential to more negative values with increase in rotation rate was observed, which can be ascribed to a chemical step. The chemical step involves the dimerization process of the binuclear oxo-manganese complex to tetranuclear oxo-manganeses complex. (C) 2014 Elsevier B.V. All rights reserved.
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.languageeng
dc.publisherElsevier B.V.
dc.relationInorganica Chimica Acta
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiomimetic
dc.subjectOxo-manganese complexes
dc.subjectRotating disk electrode
dc.subjectChange transfer mechanism
dc.subjectTafel behavior
dc.titleA comparison of charge-transfer mechanisms at rotated disk electrode for biomimetic binuclear and tetranuclear oxo-manganese complex in aqueous solution
dc.typeOtro


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