Voltammetric characterization of [ReO]3+ containing complexes
In the present work, the voltammetric profiles of Au-pc in 1 mM solutions of K[Re<SUP>V</SUP>OCl<SUB>2</SUB>(L)] (L = dianions of H<SUB>2</SUB>hida or H<SUB>2</SUB>eida; hida, n-(2,6-dimethylphenyl carbamoylmethyl)imino diacetic acid, and eida, 2,6-die...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2007 |
| País: | Argentina |
| Institución: | Universidad Nacional de La Plata |
| Repositorio: | SEDICI (UNLP) |
| Idioma: | inglés |
| OAI Identifier: | oai:sedici.unlp.edu.ar:10915/83370 |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/83370 |
| Access Level: | acceso abierto |
| Palabra clave: | Ciencias Exactas solutions complexes rhenium |
| Sumario: | In the present work, the voltammetric profiles of Au-pc in 1 mM solutions of K[Re<SUP>V</SUP>OCl<SUB>2</SUB>(L)] (L = dianions of H<SUB>2</SUB>hida or H<SUB>2</SUB>eida; hida, n-(2,6-dimethylphenyl carbamoylmethyl)imino diacetic acid, and eida, 2,6-diethyl ida) complexes were evaluated. The obtained electrochemical response was the result of the contributions coming from the [ReO]<SUP>3+</SUP> <i>core</i> (E<SUB>pa</SUB> at ca. 0.2 V vs. Ag/AgNO<SUB>3</SUB>) and the carboxylic group of the ligand. There where also observed redox contributions ascribed to the presence of perrhenate coming from the decomposition of the complex with the lost of ligands, in agreement with the low stability of the studied complexes. copyright The Electrochemical Society. |
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