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• W4242501198 abstract "Abstract The tripyrrin‐1,14‐dione scaffold of urinary pigment uroerythrin coordinates divalent palladium as a planar tridentate ligand. Spectroscopic, structural and computational investigations reveal that the tripyrrindione ligand binds as a dianionic radical, and the resulting complex is stable at room temperature. One‐electron oxidation and reduction reactions do not alter the planar coordination sphere of palladium(II) and lead to the isolation of two additional complexes presenting different redox states of the ligand framework. Unaffected by stability problems common to tripyrrolic fragments, the tripyrrindione ligand offers a robust platform for ligand‐based redox chemistry." @default.
• W4242501198 created "2022-05-12" @default.
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• W4242501198 date "2015-10-08" @default.
• W4242501198 modified "2023-10-03" @default.
• W4242501198 title "Tripyrrindione as a Redox‐Active Ligand: Palladium(II) Coordination in Three Redox States" @default.
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• W4242501198 doi "https://doi.org/10.1002/ange.201507302" @default.
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