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Method to Predict Reagents in Iridium-Based Photoredox Catalysis

preprint
submitted on 06.10.2020 and posted on 07.10.2020 by Antoine Juneau, Taylor O. Hope, Jason Malenfant, Mihai Mesko, Jacob A. Mcneill, Mathieu Frenette
Visible-light photoredox catalysts with oxidizing excited states have been broadly applied in organic synthesis. Following photon absorption by the photocatalyst, electron transfer from an organic reagent is the most common mechanistic outcome for this class of reaction. Reduction potentials for organic reagents are therefore useful to predict reactivity and DFT proved to be useful as a predictive tool in this regard. Due to the complex mechanisms that follow electron transfer, kinetics play a crucial role in the success of photoredox reactions. We extend the predictive tools of DFT to estimate the electron transfer rates between an excited photocatalyst and various organic substrates. To calibrate our model, 49 electron transfer rate constants were experimentally measured in acetonitrile for the catalyst Ir[dF(CF3)ppy]2(dtbpy)+. The rate constants, kq, gave a clear predictive trend when compared to calculated ionization energies in “frozen solvent”, which was a better predictor than standard reduction potentials in our case. The calculated kq gave an average error of 17% for log(kq) values between 4 and 11. This simple method can predict the reactivity of hundreds of reagents in silico. Notably, the calculations offered unexpected insight that we could translate into success for the C-H activation of acetylacetone as a proof-of-concept.

History

Email Address of Submitting Author

frenette.mathieu@uqam.ca

Institution

Université du Québec à Montréal

Country

Canada

ORCID For Submitting Author

0000-0003-0491-6879

Declaration of Conflict of Interest

None

Exports