Journal
INORGANIC CHEMISTRY FRONTIERS
Volume 1, Issue 8, Pages 562-576Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4qi00053f
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Photoredox catalysis by well-known ruthenium(II) polypyridine complexes and the relevant Ir cyclometalated derivatives has become a powerful tool for redox reactions in synthetic organic chemistry, because they can effectively catalyze single-electron-transfer (SET) processes by irradiation with visible light. Remarkably, since 2008, this photocatalytic system has gained importance in radical reactions from the viewpoint of not only a useful and selective protocol but also green chemistry. In this review, we will describe recent developments of radical reactions involving various carbon-centered radicals through photoredox processes mediated by Ru-and Ir-based photocatalysts.
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