Abstract
We present a red light-activated zincII bis(dipyrrin) symmetry breaking charge transfer (SBCT) architecture, showing a large molar absorption coefficient (ε = 15.4 × 104 M−1 cm−1), high reactive singlet oxygen generation efficiency (ΦΔ ≈ 0.8) and long-lived triplet state (τT = 150 μs) compared to the donor–acceptor analogue dipyrrin-BF2 complex, highlighting the superiority of the SBCT approach. For the first time, we demonstrated the potential of a SBCT scaffold in red-light-induced methyl methacrylate (MMA) polymerization, using a dual photocatalyst excitation approach.
Funding Information
  • National Natural Science Foundation of China (22350410384)
  • Basic and Applied Basic Research Foundation of Guangdong Province (2022B1515020041)
  • Dalian University of Technology (DUT2022TB10)

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