Maiti, AvijitElvers, Benedict J.Bera, SachinathLindl, FelixKrummenacher, IvoGhosh, PrasantaBraunschweig, HolgerYıldız, Cem B.Schulzke, Carola2024-05-072024-05-0720230947-65391521-3765https:/dx.doi.org10.1002/chem.202302848https://hdl.handle.net/20.500.12451/11791The authors would like to correct a misassignment of an EPR spectrum in the title paper (https://doi.org/10.1002/chem. 202104567). The authors of the original paper reported the one-electron oxidation of the cyclic(alkyl)(amino)carbene (CAAC) 1 to produce the intermediate iminium radical cation 2, as deduced from the high isolated yield of the hydrogen abstraction product 3 (Figure 1). By low-temperature (200 K) EPR spectroscopy, we observed a weak transient, three-line EPR spectrum with a g-factor of 2.0043 and a 14N hyperfine splitting (hfs) of a( 14N)=5.9 G, which we attributed to the radical cation 2 (the spectrum was depicted as Figure 1b, in the TOC cover image, in the Cover Feature (https://doi.org/10.1002/chem. 202201219), and as Figure S46 of the original paper). However, as one of the present authors (H.G.K.) later pointed out, the foregoing EPR parameters, in particular the g-factor, would not be in agreement with the proposed vinyl-type ?-radical cation.eninfo:eu-repo/semantics/embargoedAccessDisclosing Cyclic(Alkyl)(Amino)CarbenesComment on "Disclosing Cyclic(Alkyl)(Amino)Carbenes as a One-Electron Reductant: Synthesis of Acyclic(Amino)(Aryl)Carbene-Based Kekulé Diradicaloids"Letter2968