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Authordc.contributor.authorDe Souza, Antonio A. 
Authordc.contributor.authorDe Moura, Maria Aline B.F. 
Authordc.contributor.authorDe Abreu, Fabiane C. 
Authordc.contributor.authorGoulart, Marília O. F. 
Authordc.contributor.authorDa Silva, Eufrânio N. 
Authordc.contributor.authorPinto, Antonio V. 
Authordc.contributor.authorFerreira, Vitor F. 
Authordc.contributor.authorMoscoso Cabello, Raúl Andrés 
Authordc.contributor.authorNúñez Vergara, Luis
Authordc.contributor.authorSquella Serrano, Juan 
Cita de ítemdc.identifier.citationQuimica Nova, Volumen 33, Issue 10, 2018, Pages 2075-2079
Abstractdc.description.abstractThe electrochemistry of 2,2-dimethyl-(3H)-3-(N-3'-nitrophenylamino) naphtho[1,2-b]furan-4,5-dione ([Q]-PhNO2), on mercury was investigated. The first peak is consistent with a quasi-reversible one-electron reduction of the ortho-quinone, forming [Q·-]-PhNO 2, while the second one, bielectronic, corresponds to the simultaneous reduction of the latter radical to a dianion and the nitro group to a nitro radical anion. The second order rate constant, kdisp, for the decay of [Q·-]-PhNO2 is 15.188 × 10 3 ± 827 mol-1 L s-1 and the t 1/2 equals 0.06 s. E17Ic values for [Q]-PhNO2 and its precursor, nor-β-lapachone, are similar. The ease of semiquinone generation and its stability are parameters statistically relevant in the correlation biochemical/theoretical aspects.
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.uri
Sourcedc.sourceQuimica Nova
Keywordsdc.subjectSemiquinone stability
Títulodc.titleElectrochemical study, on mercury, of a Meta-nitroarylamine derivative of nor-β-lapachone, an antitumor and trypanocidal compound
Document typedc.typeArtículo de revista
Indexationuchile.indexArtículo de publicación SCOPUS

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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile