4.8 Article

Visible-Light-Driven Oxidation of Organic Substrates with Dioxygen Mediated by a [Ru(bpy)3]2+/Laccase System

Journal

CHEMSUSCHEM
Volume 8, Issue 18, Pages 3048-3051

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201500602

Keywords

copper; enzyme catalysis; olefins; oxidation; ruthenium

Funding

  1. Ministere de l'Education Nationale fellowship
  2. PACA region [DEB10-924 2010-12144]
  3. Agence Nationale de la Recherche [ANR-08-JCJC-0107-01, ANR-09-BLANC-0176]
  4. Agence Nationale de la Recherche (ANR) [ANR-08-JCJC-0107] Funding Source: Agence Nationale de la Recherche (ANR)

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Oxidation reactions are highly important chemical transformations that still require harsh reaction conditions and stoichiometric amounts of chemical oxidants that are often toxic. To circumvent these issues, olefins oxidation is achieved in mild conditions upon irradiation of an aqueous solution of the complex [Ru(bpy)(3)](2+) and the enzyme laccase. Epoxide formation is coupled to the light-driven reduction of O-2 by [Ru(bpy)(3)](2+)/laccase system. The reactivity can be explained by dioxygen acting both as an oxidative agent and as renewable electron acceptor, avoiding the use of a sacrificial electron acceptor.

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