Abstract
Using our recent relevant results, this account shows the featured reactivities of two-molecule photoredox systems compared to one-molecule photoredox systems. The low efficiency of electron transfer processes, such as photoinduced and back-electron transfer, in the two-molecule photoredox system, furnishes unique products through different pathways. The facile replacement of photoredox catalysts with appropriate oxidation/reduction potentials in this system provides valuable insights into photoredox reactions.
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