| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10575139 | Journal of Organometallic Chemistry | 2005 | 10 Pages |
Abstract
The reaction of the dilithium salt of the bridging ligand 2,9-dimethyl-1,10-dihydro-dicyclopenta[a,h]naphthalene with two equivalents of Cp*Fe(acetylacetonate) gives the complex 1 whose structure determination was carried by X-ray crystallography. Oxidation of 1 with ferrocenium affords the corresponding mixed valence compound 2 that exhibits an absorption band at 850Â nm. Cyclic voltammetry shows a potential difference of 348Â mV between both redox peaks. The Mössbauer investigations at different temperatures show a unique Fe2+ environment for the neutral compound, whereas two sites appear in the mono-oxidized compound which are assigned to Fe2+ and Fe3+.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
M.K. Amshumali, Ivonne Chávez, Verónica Arancibia, F. Burgos O, Juan M. ManrÃquez, Elies Molins, Anna Roig,
![First Page Preview: Synthesis, characterization and structure of diiron organometallic derivatives of 2,9-dimethyl-1,10-dihydro-dicyclopenta[a,h]naphthalene Synthesis, characterization and structure of diiron organometallic derivatives of 2,9-dimethyl-1,10-dihydro-dicyclopenta[a,h]naphthalene](/preview/png/10575139.png)