Elucidating the Mechanism of Excited State Bond Homolysis in Nickel–Bipyridine Photoredox Catalysts
Abstract
Ni 2,2'–bipyridine (bpy) complexes are commonly employed photoredox catalysts of bond-forming reactions in organic chemistry. However, the mechanisms by which they operate are still under investigation. One potential mode of catalysis is via entry into Ni(I)/Ni(III) cycles, which can be made possible by light-induced, excited state Ni(II)–C bond homolysis. Here we report experimental and computational analyses of a library of Ni(II)-bpy aryl halide complexes, Ni(Rbpy)(R′Ph)Cl (R = MeO, t-Bu, H, MeOOC; R′ = CH₃, H, OMe, F, CF₃), to illuminate the mechanism of excited state bond homolysis. At given excitation wavelengths, photochemical homolysis rates span two orders of magnitude across these structures and correlate linearly with Hammett parameters of both bpy and aryl ligands, reflecting structural control over key metal-to-ligand charge transfer (MLCT) and ligand-to-metal charge transfer (LMCT) excited state potential energy surfaces (PESs). Temperature- and wavelength-dependent investigations reveal moderate excited state barriers (ΔH‡ ~4 kcal mol⁻¹) and a minimum energy excitation threshold (~55 kcal mol⁻¹, 525 nm), respectively. Correlations to electronic structure calculations further support a mechanism in which repulsive triplet excited state PESs featuring a critical aryl-to-Ni LMCT lead to bond rupture. Structural control over excited state PESs provides a rational approach to utilize photonic energy and leverage excited state bond homolysis processes in synthetic chemistry.
Additional Information
The content is available under CC BY NC ND 4.0 License. D.A.C. is a National Science Foundation Graduate Research Fellow (DGE-1745301) and is supported by a National Academies of Science, Engineering, and Medicine Ford Foundation Predoctoral Fellowship. B.S. acknowledges funding through a Southern California Edison WAVE fellowship at Caltech. N.P.K. acknowledges support from the Hertz Fellowship and from the National Science Foundation Graduate Research Fellowship under Grant No. DGE-1745301. This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 883987 (D.B.). Support has been provided by the National Institutes of Health (National Institute of General Medical Sciences, R35–GM142595). We also acknowledge M. K. Takase in the Beckman Institute X-ray crystallography facility. The computations presented here were conducted in the Resnick High Performance Computing Center, a facility supported by Resnick Sustainability Institute at the California Institute of Technology. The author(s) have declared they have no conflict of interest with regard to this content. The author(s) have declared ethics committee/IRB approval is not relevant to this content.Attached Files
Submitted - 10.26434_chemrxiv-2021-g0dc2.pdf
Supplemental Material - supporting-information.pdf
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Additional details
- Eprint ID
- 112351
- Resolver ID
- CaltechAUTHORS:20211209-231174000
- DGE-1745301
- NSF Graduate Research Fellowship
- Ford Foundation
- Caltech WAVE Fellowship
- 883987
- Marie Curie Fellowship
- R35-GM142595
- NIH
- Resnick Sustainability Institute
- Southern California Edison (SCE)
- Created
-
2021-12-10Created from EPrint's datestamp field
- Updated
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2023-03-24Created from EPrint's last_modified field
- Caltech groups
- Resnick Sustainability Institute