Evidence for a Unifying Ni<sup>I</sup>/Ni<sup>III</sup> Mechanism in Light-Mediated Cross-Coupling Catalysis

Advances in nickel catalysis have significantly broadened the synthetic chemists' toolbox, particularly through methodologies leveraging paramagnetic nickel species via photoredox catalysis or electrochemistry. Key to these reactions is the oxidation state modulation of nickel via single-electron transfer events. Recent mechanistic studies indicate that C(sp<sup>2</sup>)-heteroatom bond formations proceed through Ni<sup>I</sup>/Ni<sup>III</sup> cycles. Related C(sp<sup>2</sup>)-C(sp<sup>3</sup>) cross-couplings operate via the photocatalytic generation of C-centered radicals and a catalytic cycle that involves Ni<sup>0</sup>, Ni<sup>I</sup>, and Ni<sup>III</sup> species. Here, we show that light-mediated nickel-catalyzed C(sp<sup>2</sup>)-C(sp<sup>3</sup>) bond formations can be carried out without using exogenous photoredox catalysts but with a photoactive ligand. In a pursuit of expanding the scope of C(sp<sup>2</sup>)-heteroatom couplings using donor-acceptor ligands, we identified a photoactive nickel complex capable of catalyzing cross-couplings between aryl halides and benzyltrifluoroborate salts. Mechanistic investigations provide evidence that transmetalation between a photochemically generated Ni<sup>I</sup> species and the organoboron compound is the key catalytic step in a Ni<sup>I</sup>/Ni<sup>III</sup> catalytic cycle under these conditions.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-04-11
DOI
https://doi.org/10.1021/jacs.4c16050
Citations
13
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
12.17

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article

Evidence for a Unifying NiI/NiIII Mechanism in Light-Mediated Cross-Coupling Catalysis

Haralds Baunis, Luca Dell’Amico, Susanne Reischauer, Tarek Al Said et al.
13 citations
Journal of the American Chemical Society
Radical Photochemical Reactions
12.17
article

Evidence for a Unifying NiI/NiIII Mechanism in Light-Mediated Cross-Coupling Catalysis

Haralds Baunis, Luca Dell’Amico, Susanne Reischauer, Tarek Al Said, Lucia Anghileri, John H. Burke, Renske M. van der Veen, C. Merschjann, Rachel F. Wallick, Callum E. Adams, Bartholomäus Pieber, Sergey A. Kovalenko, Gianluca Simionato, Aleksander R. Bena, Christos Giannoudis
article en
13 citations

Abstract

Advances in nickel catalysis have significantly broadened the synthetic chemists' toolbox, particularly through methodologies leveraging paramagnetic nickel species via photoredox catalysis or electrochemistry. Key to these reactions is the oxidation state modulation of nickel via single-electron transfer events. Recent mechanistic studies indicate that C(sp<sup>2</sup>)-heteroatom bond formations proceed through Ni<sup>I</sup>/Ni<sup>III</sup> cycles. Related C(sp<sup>2</sup>)-C(sp<sup>3</sup>) cross-couplings operate via the photocatalytic generation of C-centered radicals and a catalytic cycle that involves Ni<sup>0</sup>, Ni<sup>I</sup>, and Ni<sup>III</sup> species. Here, we show that light-mediated nickel-catalyzed C(sp<sup>2</sup>)-C(sp<sup>3</sup>) bond formations can be carried out without using exogenous photoredox catalysts but with a photoactive ligand. In a pursuit of expanding the scope of C(sp<sup>2</sup>)-heteroatom couplings using donor-acceptor ligands, we identified a photoactive nickel complex capable of catalyzing cross-couplings between aryl halides and benzyltrifluoroborate salts. Mechanistic investigations provide evidence that transmetalation between a photochemically generated Ni<sup>I</sup> species and the organoboron compound is the key catalytic step in a Ni<sup>I</sup>/Ni<sup>III</sup> catalytic cycle under these conditions.

Journal of the American Chemical SocietyVol. 147(16)
University of Padua (IT), Institute of Science and Technology Austria (AT), University of Illinois Urbana-Champaign (US), Helmholtz-Zentrum Berlin für Materialien und Energie (DE), Humboldt-Universität zu Berlin (DE), Max Planck Institute of Colloids and Interfaces (DE), Technische Universität Berlin (DE), Freie Universität Berlin (DE)
Institute of Science and Technology Austria, Deutscher Akademischer Austauschdienst, Deutsche Forschungsgemeinschaft, Austrian Science Fund, Max-Planck-Gesellschaft, Boehringer Ingelheim Stiftung, University of Illinois at Urbana-Champaign
Openalex Percentile: Top 1%
Radical Photochemical Reactions
12.17
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