Modulation of a μ‑1,2-Peroxo Dicopper(II) Intermediate by Strong Interaction with Alkali Metal Ions

• Published in: Journal of the American Chemical Society Vol. 143; no. 42; pp. 17751 - 17760
• Main Authors: Brinkmeier, Alexander, Dalle, Kristian E, D’Amore, Lorenzo, Schulz, Roland A, Dechert, Sebastian, Demeshko, Serhiy, Swart, Marcel, Meyer, Franc
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 27-10-2021
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.1c08645

The properties of metal/dioxygen species, which are key intermediates in oxidation catalysis, can be modulated by interaction with redox-inactive Lewis acids, but structural information about these adducts is scarce. Here we demonstrate that even mildly Lewis acidic alkali metal ions, which are typically viewed as innocent “spectators”, bind strongly to a reactive cis-peroxo dicopper­(II) intermediate. Unprecedented structural insight has now been obtained from X-ray crystallographic characterization of the “bare” CuII 2(μ-η1:η1-O2) motif and its Li+, Na+, and K+ complexes. UV–vis, Raman, and electrochemical studies show that the binding persists in MeCN solution, growing stronger in proportion to the cation’s Lewis acidity. The affinity for Li+ is surprisingly high (∼70 × 104 M–1), leading to Li+ extraction from its crown ether complex. Computational analysis indicates that the alkali ions influence the entire Cu-OO-Cu core, modulating the degree of charge transfer from copper to dioxygen. This induces significant changes in the electronic, magnetic, and electrochemical signatures of the Cu2O2 species. These findings have far-reaching implications for analyses of transient metal/dioxygen intermediates, which are often studied in situ, and they may be relevant to many (bio)­chemical oxidation processes when considering the widespread presence of alkali cations in synthetic and natural environments.