<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Han G</submitter><pubmed_abstract>One-photon-absorbing photosensitizers are commonly used in homogeneous photocatalysis which require the absorption of ultraviolet (UV) /visible light to populate the desired excited states with adequate energy and lifetime. Nevertheless, the limited penetration depth and competing absorption by organic substrates of UV/visible light calls upon exploring the utilization of longer-wavelength irradiation, such as near-infrared light (λ&lt;sub>irr&lt;/sub> > 700 nm). Despite being found applications in photodynamic therapy and bioimaging, two-photon absorption (TPA), the simultaneous absorption of two photons by one molecule, has been rarely explored in homogeneous photocatalysis. Herein, we report a group of ruthenium polypyridyl complexes possessing TPA capability that can drive a variety of organic transformations upon irradiation with 740 nm light. We demonstrate that these TPA ruthenium complexes can operate in an analogous manner as one-photon-absorbing photosensitizers for both energy-transfer and photoredox reactions, as well as function in concert with a transition metal co-catalyst for metallaphotoredox C-C coupling reactions.</pubmed_abstract><journal>Nature communications</journal><pagination>2288</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9051202</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Two-photon-absorbing ruthenium complexes enable near infrared light-driven photocatalysis.</pubmed_title><pmcid>PMC9051202</pmcid><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Han G</pubmed_authors><pubmed_authors>Han C</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Turro C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Two-photon-absorbing ruthenium complexes enable near infrared light-driven photocatalysis.</name><description>One-photon-absorbing photosensitizers are commonly used in homogeneous photocatalysis which require the absorption of ultraviolet (UV) /visible light to populate the desired excited states with adequate energy and lifetime. Nevertheless, the limited penetration depth and competing absorption by organic substrates of UV/visible light calls upon exploring the utilization of longer-wavelength irradiation, such as near-infrared light (λ&lt;sub>irr&lt;/sub> > 700 nm). Despite being found applications in photodynamic therapy and bioimaging, two-photon absorption (TPA), the simultaneous absorption of two photons by one molecule, has been rarely explored in homogeneous photocatalysis. Herein, we report a group of ruthenium polypyridyl complexes possessing TPA capability that can drive a variety of organic transformations upon irradiation with 740 nm light. We demonstrate that these TPA ruthenium complexes can operate in an analogous manner as one-photon-absorbing photosensitizers for both energy-transfer and photoredox reactions, as well as function in concert with a transition metal co-catalyst for metallaphotoredox C-C coupling reactions.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-19T00:43:00.224Z</modification><creation>2025-04-07T11:45:24.87Z</creation></dates><accession>S-EPMC9051202</accession><cross_references><pubmed>35484148</pubmed><doi>10.1038/s41467-022-29981-3</doi></cross_references></HashMap>