PHOTOCHEMICAL AND ELECTROCHEMICAL PROPERTIES OF TE COMPLEXES cis-[Co(N2O2)(acac)]
✍ Scribed by J. šima; A. Kotočová; R. Germuša; P. Kubát; P. Engst
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 395 KB
- Volume
- 103
- Category
- Article
- ISSN
- 0037-9646
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✦ Synopsis
Abstract
The complexes cis‐[Co(N~2~O~2~)(acac)], (where N~2~O~2~ = tetradentate dianionic open‐chain ligands of acacen, salen or benacen‐type; acac = 2,4‐pentadionate anion) undergo photoredox reactions under the influence of ultraviolet radiation giving rise to Co(II). The quantum yield values of the Co(III) reduction, associated with the oxidation of the acac ligand, depend on the periphery (substituents R) of the N~2~O~2~‐ligands and the wavelength of incident light. The complexes are luminescent from their intraligand excited states.
In acetonitrile solution the complexes exhibit an electrochemical oxidation response (E~pa~: 0.86 to 1,02 V vs SCE) of primarily ligand oxidation origin. A linear correlation has been obtained between the anodic peak potential, E~pa~ and the inductive parameter,σ of the substituents R. The electrochemical reduction of the complexes was poorly resolved or missing within the solvent limit.
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