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[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
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Sensitization-Initiated Electron Transfer for Photoredox Catalysis
Indrajit Ghosh1, Rizwan S Shaikh1, Burkhard König1
1Universität Regensburg, Fakultät für Chemie und Pharmazie, 93040, Regensburg, Germany.
Angewandte Chemie (International Ed. in English)
|May 26, 2017
Summary
This study introduces a two-molecule photoredox catalysis system. It mimics natural photosynthesis to enable efficient light harvesting and redox reactions using visible light for new chemical bond formations.
Area of Science:
- Chemistry
- Photocatalysis
- Organic Synthesis
Background:
- Photosynthetic organisms use antenna chromophores for light absorption and energy transfer.
- Conventional photoredox catalysis uses a single molecule for both light absorption and redox reactions.
Purpose of the Study:
- To develop a two-center photoredox catalytic system mimicking biological energy flow.
- To enable the use of molecules that do not absorb visible light in photoredox catalysis.
Main Methods:
- Utilized a ruthenium complex (Ru(bpy)3Cl2) for visible light absorption.
- Employed polycyclic aromatic hydrocarbons as energy acceptors to initiate electron transfer.
- Demonstrated sensitization-initiated electron transfer for arene activation.
Main Results:
- Successfully separated light harvesting and redox functions into two distinct molecules.
- Enabled photoredox applications for arenes like anthracene and pyrene.
- Achieved reductive activation of chemical bonds with high reduction potentials.
Conclusions:
- The developed two-center photoredox catalysis approach offers a novel strategy for visible-light-driven chemical transformations.
- This method broadens the scope of substrates for photoredox catalysis, including those with high reduction potentials.
- The approach facilitates efficient carbon-carbon and carbon-heteroatom bond formations.
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