Triplet-Triplet Energy Transfer: A Simple Strategy for an Efficient Visible Light-Induced Photoclick Reaction.

Angew Chem Int Ed Engl

Centre for Systems Chemistry, Stratingh Institute for Chemistry, Faculty for Science and Engineering, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands.

Published: May 2024

AI Article Synopsis

  • Photoclick reactions leverage both light-driven processes and click chemistry for applications like surface functionalization and protein labeling, but they mainly rely on UV light, which can cause issues like degradation of other molecules.
  • The authors propose a new method using triplet-triplet energy transfer to enable these reactions with visible light, specifically showcasing the effectiveness of 9,10-phenanthrenequinones (PQs) reacting with electron-rich alkenes (ERAs) under various light wavelengths.
  • By developing an ortho-photoclick reaction system that responds to different colors of light, the product outcome can be finely tuned, allowing for more control in chemical reactions.

Article Abstract

Photoclick reactions combine the advantages offered by light-driven processes and classical click chemistry and have found applications ranging from surface functionalization, polymer conjugation, photo-crosslinking, and protein labeling. Despite these advances, the dependency of most of the photoclick reactions on UV light poses a severe obstacle for their general implementation, as this light can be absorbed by other molecules in the system resulting in their degradation or unwanted reactivity. However, the development of a simple and efficient system to achieve bathochromically shifted photoclick transformations remains challenging. Here, we introduce triplet-triplet energy transfer as a fast and selective way to enable visible light-induced photoclick reactions. Specifically, we show that 9,10-phenanthrenequinones (PQs) can efficiently react with electron-rich alkenes (ERAs) in the presence of a catalytic amount (as little as 5 mol %) of photosensitizers. The photocycloaddition reaction can be achieved under green (530 nm) or orange (590 nm) light irradiation, representing a bathochromic shift of over 100 nm as compared to the classical PQ-ERAs system. Furthermore, by combining appropriate reactants, we establish an orthogonal, blue and green light-induced photoclick reaction system in which the product distribution can be precisely controlled by the choice of the color of light.

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Source
http://dx.doi.org/10.1002/anie.202319321DOI Listing

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