Demonstrates the electronic behavior of ruthenium complexes in noncoordinating solvents, highlighting implications for catalysis.
Half-sandwich ruthenium(II) complexes supported by phosphine ligands typically undergo one-electron oxidation processes at potentials that depend on the identity of the phosphine ligand. While in noncoordinating solvents these electron transfer (ET) processes are often
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Fumo et al. (2026) studied this question.
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