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dc.creatorARMIJO,FRANCISCO
dc.creatorAGUIRRE,MARÍA J
dc.date2005-03-01
dc.date.accessioned2020-02-17T15:35:34Z
dc.date.available2020-02-17T15:35:34Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-97072005000100002
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/131967
dc.descriptionPorphyrins and phthalocyanines of transition metals are good catalysts for many redox reactions [<A HREF="#1">1</A>-<A HREF="#7">7</A>]. In order to increase their catalytic activity it is often necessary to modify the macrocycle with donor or acceptor substituents making the species more reductive or oxidant depending on the analyte. However, this process is a one-way modification, because the molecule enhances or diminishes the electronic density of the metal by the substituent effect
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0717-97072005000100002
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceJournal of the Chilean Chemical Society v.50 n.1 2005
dc.titleElectrocatalysis of NO2- on poly-M-tetraaminophenylporphyrines (M = Ni, Cu) modified electrodes assisted by visible light


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