4.8 Article

Upconversion-like Photolysis of BODIPY-Based Prodrugs via a One-Photon Process

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 44, Pages 17482-17486

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b09034

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Funding

  1. Seed Fund for Basic Research of The University of Hong Kong [201711159053]
  2. Guangdong-Hong Kong Technology Cooperation Funding Scheme [2017A050506016]
  3. Young Scientists Fund of the National Natural Science Foundation of China [81803469]
  4. University of Hong Kong

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Photochemical reactions at lower energy than the absorption window are currently achieved by multi-photon processes, including two-photon absorption and photon upconversion, which have limited energy utilization efficiency. Here, we report a one-photon strategy based on triplet triplet-energy transfer (TTET) between a photosensitizer and a photocleavable molecule to achieve photolysis at low energy. To verify this concept, we chose platinum(II) tetraphenyltetrabenzoporphyrin (PtTPBP) as the photosensitizer and synthesized a boron-dipyrromethene (BODIPY)-based prodrug as the photocleavable molecule. Photolysis of the prodrug is achieved by TTET upon excitation of PtTPBP at 625 nm with a photolysis quantum yield of 2.8%. Another demonstration shows an unexpected higher photolysis quantum yield than the direct excitation at 530 nm. This strategy opens a new path for achieving photolysis at long wavelengths, benefiting the applications in biological studies, photopharmacology, and photoresponsive drug delivery.

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