Faycel Djebbar, Lise-Marie Chamoreau and Guillaume Lefèvre*,
{"title":"Influence of a Two-Fold Ligation Pattern on Iron-Mediated Aryl–Heteroaryl Cross-Electrophile Couplings","authors":"Faycel Djebbar, Lise-Marie Chamoreau and Guillaume Lefèvre*, ","doi":"10.1021/jacsau.5c0005910.1021/jacsau.5c00059","DOIUrl":null,"url":null,"abstract":"<p >An aryl–heteroaryl cross-electrophile coupling (XEC) relying on the use of a single, well-defined iron catalyst is disclosed, involving magnesium as an electron source as well as heteroaryl chlorides and aryl iodides or bromides as coupling partners. A 2-fold coordination pattern featuring a π-acceptor, redox-active (N,N) ligand, along with a σ-donating phosphine ensures both the two-electron reduction of the starting iron(II) precursor to enter the cycle and access to stable organoiron(II) resting states, inhibiting the reductive decomposition of the catalyst.</p>","PeriodicalId":94060,"journal":{"name":"JACS Au","volume":"5 5","pages":"2135–2147 2135–2147"},"PeriodicalIF":8.5000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/jacsau.5c00059","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JACS Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacsau.5c00059","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
An aryl–heteroaryl cross-electrophile coupling (XEC) relying on the use of a single, well-defined iron catalyst is disclosed, involving magnesium as an electron source as well as heteroaryl chlorides and aryl iodides or bromides as coupling partners. A 2-fold coordination pattern featuring a π-acceptor, redox-active (N,N) ligand, along with a σ-donating phosphine ensures both the two-electron reduction of the starting iron(II) precursor to enter the cycle and access to stable organoiron(II) resting states, inhibiting the reductive decomposition of the catalyst.