Show simple item record

Authordc.contributor.authorMerino, M. 
Authordc.contributor.authorCarbajo, J. es_CL
Authordc.contributor.authorNúñez Vergara, Luis es_CL
Authordc.contributor.authorSquella Serrano, Juanes_CL
Admission datedc.date.accessioned2009-05-20T17:07:23Z
Available datedc.date.available2009-05-20T17:07:23Z
Publication datedc.date.issued2000-03
Cita de ítemdc.identifier.citationBOLETIN DE LA SOCIEDAD CHILENA DE QUIMICA 45(1):91-97en
Identifierdc.identifier.issn0366-1644
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120616
Abstractdc.description.abstractThe electrochemical nitroreduction of nitrofurantoin has been studied on carbon paste and glassy carbon electrodes. We can observe a monoelectronic reversible couple ArNO2/ArNO2- and an irreversible peak due to the further reduction of nitro radical to the hidroxilamine via three electrons. According to the experimental results, the reduction process shows a typical behavior of an EC mechanism. The k(2) obtained values showed that the nitroradical anion was better stabilized on carbon paste electrode.en
Lenguagedc.language.isoenen
Publisherdc.publisherSOCIEDAD CHILENA DE QUIMICAen
Keywordsdc.subjectNITRO-HETEROCYCLIC COMPOUNDSen
Títulodc.titleNitroradical anion formation from nitrofurantoin in carbon electrodesen
Document typedc.typeArtículo de revista


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record