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Authordc.contributor.authorNúñez Vergara, Luis es_CL
Authordc.contributor.authorBollo Dragnic, Soledad es_CL
Authordc.contributor.authorOlea Azar, Claudio es_CL
Authordc.contributor.authorSantander, Paola es_CL
Authordc.contributor.authorGunckel, Soledades_CL
Authordc.contributor.authorSquella Serrano, Juan
Admission datedc.date.accessioned2011-07-25T12:53:39Z
Available datedc.date.available2011-07-25T12:53:39Z
Publication datedc.date.issued1998
Cita de ítemdc.identifier.citationBoletín de la Sociedad Chilena de Química 43 (2): 231-239es_CL
Identifierdc.identifier.issn0366-1644
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121458
Abstractdc.description.abstractThis paper reports the scavenging of the nitro radical anion of nisoldipine by N-acetylcysteine assessed by cyclic volatammetry (CV) and EPR spectroscopic techniques. Studies by CV on the reactivity of the radical were conducted on the mercury electrode in mixed media at pH 9.0 (0.012 M aqueous citrate buffer/DMF 40/60, 0.1 M TBAI). Interaction rate constant was significantly higher than that on the second order decay rate constant of the radical (ki=4.857[Msec]-1. EPR spectra recorded in situ using DMF/0.1 N NaOH (pH 13) of the nitro radical anion from nisoldipine electrochemically generated was completely inhibited for a 20 mM concentration of N-acetylcysteinees_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherSociedad Chilena de Químicaes_CL
Keywordsdc.subjectNitro radical aniones_CL
Títulodc.titleReactivity of the nitro radical anion from nisoldipine with N-acetylcysteine: EPR spectroscopic and electrochemical evidencees_CL
Document typedc.typeArtículo de revista


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