Author | dc.contributor.author | Torres, Simonet | |
Author | dc.contributor.author | Ferraudi, Guillermo | es_CL |
Author | dc.contributor.author | Aguirre, María Jesús | es_CL |
Author | dc.contributor.author | Isaacs Casanova, Mauricio | es_CL |
Author | dc.contributor.author | Matsuhiro, Betty | es_CL |
Author | dc.contributor.author | Chandía, Nancy P. | es_CL |
Author | dc.contributor.author | Mendoza, Leonora | es_CL |
Admission date | dc.date.accessioned | 2011-12-21T20:23:34Z | |
Available date | dc.date.available | 2011-12-21T20:23:34Z | |
Publication date | dc.date.issued | 2011 | |
Cita de ítem | dc.identifier.citation | Helvetica Chimica Acta – Vol. 94 (2011) | es_CL |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/119378 | |
General note | dc.description | Artículo de publicación ISI | es_CL |
Abstract | dc.description.abstract | In contrast to the UV-photoinduced ligand photoionization of the flavonoid complexes of FeIII,
redox reactions initiated in ligand-to-metal charge-transfer excited states were observed on irradiation of
the quercetin (1) and rutin (2) complexes of CuII. Solutions of complexes with stoichiometries [CuIIL2]
(L¼quercetin, rutin) and [CuII
2Ln] (n¼1, L¼quercetin; n¼3, L¼rutin) were flash-irradiated at
351 nm. Transient spectra observed in these experiments showed the formation of radical ligands
corresponding to the one-electron oxidation of L and the reduction of CuII to CuI. The radical ligands
remained coordinated to the CuI centers, and the substitution reactions replacing them by solvent
occurred with lifetimes t<350 ns. These are lifetimes shorter than the known lifetimes (t>1 ms) of the
quercetin and rutin radical s decay. | es_CL |
Lenguage | dc.language.iso | en | es_CL |
Título | dc.title | On the Ligand-to-Metal Charge-Transfer Photochemistry of the Copper(II) Complexes of Quercetin and Rutin | es_CL |
Document type | dc.type | Artículo de revista | |