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Electron transfer in a covalent dye-cobalt catalyst assembly - a transient absorption spectroelectrochemistry
Sebastian Bold1, Linda Zedler2, Ying Zhang3
1Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich Schiller University Jena, Helmholtzweg 4, 07743 Jena, Germany and Department Functional Interfaces, Leibniz Institute of Photonic Technology Jena (IPHT), Albert-Einstein-Straße 9, 07745 Jena, Germany. benjamin.dietzek@leibniz-ipht.de and Laboratoire de Chimie et Biologie des Métaux, Université Grenoble Alpes, CNRS, CEA, 17 rue des Martyrs, 38000 Grenoble, France. murielle.chavarot-kerlidou@cea.fr.
Abstract:
Various oxidation states of the catalytically active cobalt center in a covalent dyad were electrochemically prepared and the light-induced excited-state processes were studied. Virtually identical deactivation processes are observed, irrespective of the oxidation state of the cobalt center, varying from CoIII to CoI, indicating the absence of oxidative quenching within the dye-catalyst assembly.
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