{"title":"Two-fold proton coupled electron transfer of a Ta(V) aniline complex mediated by a redox active NNN pincer ligand","authors":"Josh, Abbenseth, Sotirios, Pavlidis, Jasmin, Alasadi, Amanda, Opis-Basilio","doi":"10.26434/chemrxiv-2024-5rjl7","DOIUrl":null,"url":null,"abstract":"The proton coupled electron transfer reactivity of an octahedral Ta(V) aniline complex ligated by an acridane-derived redox active NNN pincer ligand is reported. Reversible association of aniline to a Ta(V) dichloride leads to significant coordination induced bond weakening of aniline’s N–H bonds allowing for two-fold hydrogen atom abstraction yielding a terminal imido complex accompanied by two-electron oxidation of the NNN pincer ligand under retention of the metal oxidation state. The bond dissociation free energies of the amine and a transient radical amido complex are estimated via stoichiometric reactions with hydrogen atom abstractor and donor reagents complemented by DFT calculations.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":"85 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-5rjl7","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
The proton coupled electron transfer reactivity of an octahedral Ta(V) aniline complex ligated by an acridane-derived redox active NNN pincer ligand is reported. Reversible association of aniline to a Ta(V) dichloride leads to significant coordination induced bond weakening of aniline’s N–H bonds allowing for two-fold hydrogen atom abstraction yielding a terminal imido complex accompanied by two-electron oxidation of the NNN pincer ligand under retention of the metal oxidation state. The bond dissociation free energies of the amine and a transient radical amido complex are estimated via stoichiometric reactions with hydrogen atom abstractor and donor reagents complemented by DFT calculations.