Abstract
Coordination of the novel redox-active phosphineappended aminophenol pincer ligand (PNOH2) to PdII generates a paramagnetic complex with a persistent ligand-centered radical. The complex undergoes fully reversible single-electron oxidation and reduction. Homolytic bond activation of diphenyldisulfide by the single-electron reduced species leads to a ligand-based mixed-valent dinuclear palladium complex with a single bridging thiolate ligand. Mechanistic investigations support an unprecedented intramolecular ligand-to-disulfide single-electron transfer process to induce homolytic S-S cleavage, thereby releasing a thiyl (sulfanyl) radical. This could be a new strategy for small-molecule bond activation.
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Broere, D. L. J., Metz, L. L., De Bruin, B., Reek, J. N. H., Siegler, M. A., & Van Der Vlugt, J. I. (2015). Redox-active ligand-induced homolytic bond activation. Angewandte Chemie - International Edition, 54(5), 1516–1520. https://doi.org/10.1002/anie.201410048
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