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Stable Mixed-Valent Radicals from Platinum(II) Complexes of a Bis(dioxolene) Ligand
Three diplatinum(II) complexes [{PtL}(2)(μ-thea)] (H(4)thea=2,3,6,7-tetrahydroxy-9,10-dimethyl-9,10-dihydro-9,10-ethanoanthracene) have been prepared, with diphosphine or bipyridyl “L” co-ligands. One-electron oxidation of these complexes gave radical cations containing a mixed-valent [thea[Image: s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164269/ https://www.ncbi.nlm.nih.gov/pubmed/24488824 http://dx.doi.org/10.1002/chem.201304848 |
Sumario: | Three diplatinum(II) complexes [{PtL}(2)(μ-thea)] (H(4)thea=2,3,6,7-tetrahydroxy-9,10-dimethyl-9,10-dihydro-9,10-ethanoanthracene) have been prepared, with diphosphine or bipyridyl “L” co-ligands. One-electron oxidation of these complexes gave radical cations containing a mixed-valent [thea[Image: see text]](3−) ligand with discrete catecholate and semiquinonate centers separated by quaternary methylene spacers. The electronic character of these radicals is near the Robin–Day class II/III border determined by UV/Vis/NIR and EPR spectroscopies. Crystal-structure determinations and a DFT calculation imply that oxidation of the thea(4−) ligand may lead to an increased through-space interaction between the dioxolene π systems. |
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