<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang X</submitter><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>2157</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924867</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Molecular triplet-triplet annihilation upconversion often experiences drastic luminescence quenching in the presence of oxygen molecules, posing a significant constraint on practical use in aerated conditions. We present an oxygen-immune near-infrared triplet-triplet annihilation upconversion system utilizing non-organometallic cyanine sensitizers (λ&lt;sub>ex&lt;/sub> = 808 nm) and chemically synthesized benzo[4,5]thieno[2,3-b][1,2,5]thiadiazolo[3,4-g]quinoxaline dyes with a defined dimer structure as annihilators (λ&lt;sub>em&lt;/sub> = 650 nm). This system exhibits ultrastable upconversion under continuous laser irradiance (>480 mins) or extended storage (>7 days) in aerated solutions. Mechanistic investigations reveal rapid triplet-triplet energy transfer from sensitizer to annihilators, accompanied by remarkably low triplet oxygen quenching efficiencies ( ηO2  &lt; 13% for the sensitizer, &lt;3.7% for the annihilator), endowing the bicomponent triplet-triplet annihilation system with inherent oxygen immunity. Our findings unlock the direct and potent utilization of triplet-triplet annihilation upconversion systems in real-world applications, demonstrated by the extended and sensitive nanosensing of peroxynitrite radicals in the liver under in vivo nitrosative stress.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Molecular near-infrared triplet-triplet annihilation upconversion with eigen oxygen immunity.</pubmed_title><pmcid>PMC10924867</pmcid><funding_grant_id>51972084</funding_grant_id><pubmed_authors>Ding F</pubmed_authors><pubmed_authors>Deng R</pubmed_authors><pubmed_authors>Ding X</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Jia T</pubmed_authors><pubmed_authors>Li F</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Lin K</pubmed_authors><pubmed_authors>Wu W</pubmed_authors><pubmed_authors>Xia D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular near-infrared triplet-triplet annihilation upconversion with eigen oxygen immunity.</name><description>Molecular triplet-triplet annihilation upconversion often experiences drastic luminescence quenching in the presence of oxygen molecules, posing a significant constraint on practical use in aerated conditions. We present an oxygen-immune near-infrared triplet-triplet annihilation upconversion system utilizing non-organometallic cyanine sensitizers (λ&lt;sub>ex&lt;/sub> = 808 nm) and chemically synthesized benzo[4,5]thieno[2,3-b][1,2,5]thiadiazolo[3,4-g]quinoxaline dyes with a defined dimer structure as annihilators (λ&lt;sub>em&lt;/sub> = 650 nm). This system exhibits ultrastable upconversion under continuous laser irradiance (>480 mins) or extended storage (>7 days) in aerated solutions. Mechanistic investigations reveal rapid triplet-triplet energy transfer from sensitizer to annihilators, accompanied by remarkably low triplet oxygen quenching efficiencies ( ηO2  &lt; 13% for the sensitizer, &lt;3.7% for the annihilator), endowing the bicomponent triplet-triplet annihilation system with inherent oxygen immunity. Our findings unlock the direct and potent utilization of triplet-triplet annihilation upconversion systems in real-world applications, demonstrated by the extended and sensitive nanosensing of peroxynitrite radicals in the liver under in vivo nitrosative stress.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T12:59:06.875Z</modification><creation>2025-04-04T12:59:06.875Z</creation></dates><accession>S-EPMC10924867</accession><cross_references><pubmed>38461161</pubmed><doi>10.1038/s41467-024-46541-z</doi></cross_references></HashMap>