4.8 Article

A Molecular Light-Driven Water Oxidation Catalyst

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 26, Pages 10721-10724

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja300797g

Keywords

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Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-FG02-07ER15888]
  2. Robert A. Welch Foundation [E-621]

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Two mononuclear Ru(II) complexes, [Ru(ttbt)(pynap)(I)]I and [Ru(tpy)(Mepy)(2)(I)]I (tpy = 2,2';6,2 ''-terpyridine; ttbt = 4,4',4 ''-tri-tert-butyltpy; pynap = 2-(pyrid-2'-yl)-1,8-naphthyridine; and Mepy = 4-methylpyridine), are effective catalysts for the oxidation of water. This oxidation can be driven by a blue (lambda(max) = 472 nm) LED light source using [Ru(bpy)(3)]Cl-2 (bpy = 2,2'-bipyridine) as the photosensitizer. Sodium persulfate acts as a sacrificial electron acceptor to oxidize the photosensitizer that in turn drives the catalysis. The presence of all four components, light, photosensitizer, sodium persulfate, and catalyst, are required for water oxidation. A dyad assembly has been prepared using a pyrazine-based linker to join a photosensitizer and catalyst moiety. Irradiation of this intramolecular system with blue Light produces oxygen with a higher turnover number than the analogous intermolecular component system under the same conditions.

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