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. 2022 May 18;13:2737. doi: 10.1038/s41467-022-30278-8

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Reaction conditions: alkyl bromide (0.2 mmol), C–H coupling partner as solvent (0.05 M, 4 mL), Ir[dF(CF₃)ppy]₂(dtbbpy)PF₆ (PS1, 2 mol%), Ni(cod)₂ (5 mol%), 4,4’-dOMe-bpy (5.5 mol%), K₂CO₃ (2 equiv.), 34 W blue LEDs, Ar, 48 h, room temperature. ^aThe reaction was performed using 2-(2-bromoethyl)-1,3-dioxolane and the final aldehyde product was obtained upon deprotection. ^bIsolated in a 5:1 ratio with the homo-coupling product of alkyl halide. ^c10 equiv. of alkyl component, benzene (0.125 M), NiCl₂ glyme (10 mol%), 4,4’-dtbbpy (11 mol%), NaHCO₃ (2 equiv.), 34 W x 2 blue LEDs, 96 h. See Supplementary Methods 3 for more details.