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The utilization of low-energy photons in light-driven reactions is an effective strategy for improving the efficiency of solar energy conversion. In nature, photosynthetic organisms use chlorophylls to harvest the red portion of sunlight, which ultimately drives the reduction of CO. However, a molecular system that mimics such function is extremely rare in non-noble-metal catalysis. Here we report a series of synthetic fluorinated chlorins as biomimetic chromophores for CO reduction, which catalytically produces CO under both 630 nm and 730 nm light irradiation, with turnover numbers of 1790 and 510, respectively. Under appropriate conditions, the system lasts over 240 h and stays active under 1% concentration of CO. Mechanistic studies reveal that chlorin and chlorinphlorin are two key intermediates in red-light-driven CO reduction, while corresponding porphyrin and bacteriochlorin are much less active forms of chromophores.
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http://dx.doi.org/10.1038/s41467-024-50084-8 | DOI Listing |
Chemistry
May 2025
School of Chemical Sciences, Indian Institute of Technology Mandi, Mandi, Himachal Pradesh, 175075, India.
Photocatalysis emerges as an efficient and versatile tool for the preparation of organic compounds via the development of new methodologies and new photosensitizers. Mostly UV and blue light irradiation are used for such reactions. Red light is low-energy light, it is less harmful and has more penetration depth.
View Article and Find Full Text PDFNat Commun
July 2024
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, IGCME, Sun Yat-sen University, Guangzhou, China.
The utilization of low-energy photons in light-driven reactions is an effective strategy for improving the efficiency of solar energy conversion. In nature, photosynthetic organisms use chlorophylls to harvest the red portion of sunlight, which ultimately drives the reduction of CO. However, a molecular system that mimics such function is extremely rare in non-noble-metal catalysis.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
May 2024
Department of Chemistry, Graduate School of Science, Nagoya University, Furo, Chikusa, 464-8602, Nagoya, Japan.
The photocatalytic reduction of carbon dioxide (CO) represents an attractive approach for solar-energy storage and leads to the production of renewable fuels and valuable chemicals. Although some osmium (Os) photosensitizers absorb long wavelengths in the visible-light region, a self-photosensitized, mononuclear Os catalyst for red-light-driven CO reduction has not yet been exploited. Here, we discovered that the introduction of an Os metal to a PNNP-type tetradentate ligand resulted in the absorption of light with longer-wavelength (350-700 nm) and that can be applied to a panchromatic self-photosensitized catalyst for CO reduction to give mainly carbon monoxide (CO) with a total turnover number (TON) of 625 under photoirradiation (λ≥400 nm).
View Article and Find Full Text PDFChem Sci
December 2022
Department of Chemistry, University of Basel St. Johanns-Ring 19 4056 Basel Switzerland
By combining the energy input from two red photons, chemical reactions that would normally require blue or ultraviolet irradiation become accessible. Key advantages of this biphotonic excitation strategy are that red light usually penetrates deeper into complex reaction mixtures and causes less photo-damage than direct illumination in the blue or ultraviolet. Here, we demonstrate that the primary light-absorber of a dual photocatalytic system comprised of a transition metal-based photosensitizer and an organic co-catalyst can completely alter the reaction outcome.
View Article and Find Full Text PDFJ Am Chem Soc
January 2022
Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C, Denmark.
Photoisomerization of retinal protonated Schiff base in microbial and animal rhodopsins are strikingly ultrafast and highly specific. Both protein environments provide conditions for fine-tuning the photochemistry of their chromophores. Here, by combining time-resolved action absorption spectroscopy and high-level electronic structure theory, we show that similar control can be gained in a synthetically engineered retinal chromophore.
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