{"title":"Protodefluorinated Selectfluor® heteroaggregate photoinduces direct C(sp3)–H fluorinations without photocatalyst†","authors":"Shahboz Yakubov , Joshua P. Barham","doi":"10.1039/d5qo00149h","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we uncover a hitherto hidden role of – a cheap, stable, recoverable by-product of radical C(sp<sup>3</sup>)–H fluorinations using Selectfluor®. This forms a photoactive, mixed heteroaggregate with Selectfluor® which underlies the reactivity of visible light photochemical fluorination reactions of unactivated C(sp<sup>3</sup>)–H bonds. Where previous reports claim to be ‘photocatalytic’, reactions work without photocatalyst when is dosed in at the start. Our results demonstrate that ‘photocatalysts’ are only necessary to generate a sufficient amount of nascent , whose heteroaggregate with Selectfluor® takes over as the main photoactive species. Mechanistic studies suggest the formation of a heteroaggregate between and Selectfluor® under photoirradiation, which generates . A salient feature of our <strong>H-TEDA(BF</strong><sub><strong>4</strong></sub><strong>)</strong><sub><strong>2</strong></sub>-promoted method is its flexibility to use the C(sp<sup>3</sup>)–H precursor substrate as the limiting reactant, simplifying product isolations.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 10","pages":"Pages 3156-3162"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412925001524","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Herein, we uncover a hitherto hidden role of – a cheap, stable, recoverable by-product of radical C(sp3)–H fluorinations using Selectfluor®. This forms a photoactive, mixed heteroaggregate with Selectfluor® which underlies the reactivity of visible light photochemical fluorination reactions of unactivated C(sp3)–H bonds. Where previous reports claim to be ‘photocatalytic’, reactions work without photocatalyst when is dosed in at the start. Our results demonstrate that ‘photocatalysts’ are only necessary to generate a sufficient amount of nascent , whose heteroaggregate with Selectfluor® takes over as the main photoactive species. Mechanistic studies suggest the formation of a heteroaggregate between and Selectfluor® under photoirradiation, which generates . A salient feature of our H-TEDA(BF4)2-promoted method is its flexibility to use the C(sp3)–H precursor substrate as the limiting reactant, simplifying product isolations.