Photocatalytic redox reactions with metalloporphyrins

Author:

Fukuzumi Shunichi12,Lee Yong-Min13,Nam Wonwoo14

Affiliation:

1. Department of Chemistry and Nano Science, Ewha Womans University, Seoul 03760, Korea

2. Faculty of Science and Engineering, Meijo University, Nagoya, Aichi 468-0073, Japan

3. Research Institute for Basic Sciences, Ewha Womans University, Seoul 03760, Korea

4. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences, Lanzhou 730000, China

Abstract

Metalloporphyrinoids are utilized as efficient sensitizers and catalysts in photosynthesis and the reverse reaction that is respiration. Because metalloporphyrinoids show strong absorption in the visible region and redox active, metalloporphyrinoids are also suited as photoredox catalysts for photo-driven redox reactions using solar energy. In particular, metalloporphyrins are utilized as pivotal components to mimic the structure and function of the photosynthetic reaction center. Metalloporphyrins are used as photoredox catalysts for hydrogen evolution from electron and proton sources combining hydrogen evolution catalysts. Metalloporphyrins also act as thermal redox catalysts for photocatalytic reduction of CO2 with photoredox catalysts. Metalloporphyrins are also used as dual catalysts for a photoredox catalyst for oxygenation of substrates with H2O and a redox catalyst for O2 reduction when dioxygen is used as a two-electron oxidant and H2O as an oxygen source, both of which are the greenest reactants. Free base porphyrins can also be employed as promising photoredox catalysts for C–C bond formation reactions.

Funder

Japan Society for the Promotion of Science

Basic Science Research Program, Korea

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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