<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gordon JB</submitter><funding>Johns Hopkins University</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>21637-21647</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9109941</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>143(51)</volume><pubmed_abstract>Addition of dioxygen at low temperature to the non-heme ferrous complex Fe&lt;sup>II&lt;/sup>(Me&lt;sub>3&lt;/sub>TACN)((OSi&lt;sup>Ph2&lt;/sup>)&lt;sub>2&lt;/sub>O) (&lt;b>1&lt;/b>) in 2-MeTHF produces a peroxo-bridged diferric complex Fe&lt;sub>2&lt;/sub>&lt;sup>III&lt;/sup>(μ-O&lt;sub>2&lt;/sub>)(Me&lt;sub>3&lt;/sub>TACN)&lt;sub>2&lt;/sub>((OSi&lt;sup>Ph2&lt;/sup>)&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub> (&lt;b>2&lt;/b>), which was characterized by UV-vis, resonance Raman, and variable field Mössbauer spectroscopies. Illumination of a frozen solution of &lt;b>2&lt;/b> in THF with white light leads to homolytic O-O bond cleavage and generation of a Fe&lt;sup>IV&lt;/sup>(O) complex &lt;b>4&lt;/b> (ν(Fe=O) = 818 cm&lt;sup>-1&lt;/sup>; δ = 0.22 mm s&lt;sup>-1&lt;/sup>, Δ&lt;i>E&lt;/i>&lt;sub>Q&lt;/sub> = 0.23 mm s&lt;sup>-1&lt;/sup>). Variable field Mössbauer spectroscopy measurements show that &lt;b>4&lt;/b> is a rare example of a high-spin &lt;i>S&lt;/i> = 2 Fe&lt;sup>IV&lt;/sup>(O) complex and the first synthetic example to be generated directly from O&lt;sub>2&lt;/sub>. Complex &lt;b>4&lt;/b> is highly reactive, as expected for a high-spin ferryl, and decays rapidly in fluid solution at cryogenic temperatures. This decay process in 2-MeTHF involves C-H cleavage of the solvent. However, the controlled photolysis of &lt;b>2&lt;/b> &lt;i>in situ&lt;/i> with visible light and excess phenol substrate leads to competitive phenol oxidation, via the proposed transient generation of &lt;b>4&lt;/b> as the active oxidant.</pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>A Reactive, Photogenerated High-Spin (&lt;i>S&lt;/i> = 2) Fe&lt;sup>IV&lt;/sup>(O) Complex via O&lt;sub>2&lt;/sub> Activation.</pubmed_title><pmcid>PMC9109941</pmcid><funding_grant_id>R01 GM119374</funding_grant_id><funding_grant_id>R01GM119374</funding_grant_id><pubmed_authors>Moenne-Loccoz P</pubmed_authors><pubmed_authors>Dey A</pubmed_authors><pubmed_authors>Bill E</pubmed_authors><pubmed_authors>Gordon JB</pubmed_authors><pubmed_authors>Albert T</pubmed_authors><pubmed_authors>Sabuncu S</pubmed_authors><pubmed_authors>Siegler MA</pubmed_authors><pubmed_authors>Goldberg DP</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Reactive, Photogenerated High-Spin (&lt;i>S&lt;/i> = 2) Fe&lt;sup>IV&lt;/sup>(O) Complex via O&lt;sub>2&lt;/sub> Activation.</name><description>Addition of dioxygen at low temperature to the non-heme ferrous complex Fe&lt;sup>II&lt;/sup>(Me&lt;sub>3&lt;/sub>TACN)((OSi&lt;sup>Ph2&lt;/sup>)&lt;sub>2&lt;/sub>O) (&lt;b>1&lt;/b>) in 2-MeTHF produces a peroxo-bridged diferric complex Fe&lt;sub>2&lt;/sub>&lt;sup>III&lt;/sup>(μ-O&lt;sub>2&lt;/sub>)(Me&lt;sub>3&lt;/sub>TACN)&lt;sub>2&lt;/sub>((OSi&lt;sup>Ph2&lt;/sup>)&lt;sub>2&lt;/sub>O)&lt;sub>2&lt;/sub> (&lt;b>2&lt;/b>), which was characterized by UV-vis, resonance Raman, and variable field Mössbauer spectroscopies. Illumination of a frozen solution of &lt;b>2&lt;/b> in THF with white light leads to homolytic O-O bond cleavage and generation of a Fe&lt;sup>IV&lt;/sup>(O) complex &lt;b>4&lt;/b> (ν(Fe=O) = 818 cm&lt;sup>-1&lt;/sup>; δ = 0.22 mm s&lt;sup>-1&lt;/sup>, Δ&lt;i>E&lt;/i>&lt;sub>Q&lt;/sub> = 0.23 mm s&lt;sup>-1&lt;/sup>). Variable field Mössbauer spectroscopy measurements show that &lt;b>4&lt;/b> is a rare example of a high-spin &lt;i>S&lt;/i> = 2 Fe&lt;sup>IV&lt;/sup>(O) complex and the first synthetic example to be generated directly from O&lt;sub>2&lt;/sub>. Complex &lt;b>4&lt;/b> is highly reactive, as expected for a high-spin ferryl, and decays rapidly in fluid solution at cryogenic temperatures. This decay process in 2-MeTHF involves C-H cleavage of the solvent. However, the controlled photolysis of &lt;b>2&lt;/b> &lt;i>in situ&lt;/i> with visible light and excess phenol substrate leads to competitive phenol oxidation, via the proposed transient generation of &lt;b>4&lt;/b> as the active oxidant.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-04-26T12:06:13.591Z</modification><creation>2025-04-06T13:52:05.578Z</creation></dates><accession>S-EPMC9109941</accession><cross_references><pubmed>34913683</pubmed><doi>10.1021/jacs.1c10051</doi></cross_references></HashMap>