Covalent Association of a Ruthenium‐Based Chromophore and a Copper Catalyst: A Synergy for Sulfides Photo‐oxidation

Author:

Klein Johannes1,Girardon Anna1,Moreno‐Betancourt Angelica2,Loiseau Frédérique2ORCID,Jouvenot Damien2ORCID,Pécaut Jacques3ORCID,Hamelin Olivier1ORCID,Torelli Stéphane1ORCID

Affiliation:

1. Univ Grenoble Alpes CNRS CEA, IRIG Laboratoire de Chimie et Biologie des Métaux 17 rue des Martyrs 38000 Grenoble France

2. Univ. Grenoble Alpes CNRS, DCM 38000 Grenoble France

3. Univ. Grenoble Alpes CEA, CNRS, INAC-SyMMES Grenoble France

Abstract

AbstractThe development of catalytic systems for the oxidation of organic substrates using renewable sources such as water and dioxygen remains challenging. In this paper we report the synthesis and full characterization of a new dyad combining a ruthenium(II)‐based chromophore and a bio‐inspired copper(II) pre‐catalyst. In particular, photo‐induced electron transfer from the photosensitized RuII subunit toward the CuII center is highlighted. The photogenerated CuI moiety proves to be catalytically efficient for sulfides oxidation by 3O2 in the presence of a sacrificial electron source. Finally, the covalent association of the two partners favors Cu/O2‐based catalysis at the expense of a 1O2‐centered reactivity for a bimolecular mixture.

Publisher

Wiley

Subject

Inorganic Chemistry

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