A stable bridge: A peroxo‐bridged Fe–O2–Cu complex (see picture) was synthesized and isolated as crystals. The X‐ray structure analysis revealed that the Fe–O2–Cu moiety has a μ‐η2:η1 coordination mode; a peroxo ligand is bound to Fe in a side‐on fashion with only one oxygen atom of the peroxide bound to Cu. The two metal ions (high‐spin FeIII and CuII) were strongly coupled in an antiferromagnetic fashion, thus resulting in a total spin of S=2.
Eine stabile Brücke: Die Fe‐O2‐Cu‐Einheit des hier beschriebenen Fe‐Cu‐Komplexes (siehe Bild) weist einen μ‐η2:η1‐Koordinationsmodus auf: Ein side‐on an das Fe‐Zentrum gebundener Peroxoligand koordiniert nur mit einem Sauerstoffatom an das Cu‐Zentrum. Zwischen beiden Metallzentren (High‐Spin‐FeIII und CuII) herrscht eine starke antiferromagnetische Kopplung; der Gesamtspin beträgt S=2.
A binucleating porphyrin with covalently appended copper chelates having a cross-linked imidazole-phenol group as the novel active site model of cytochrome c oxidase has been prepared, and the dioxygen adduct of its iron(II)-copper(I) complex was spectroscopically characterized.
The title compound, C10H10N2O, was synthesized to investigate the structure of the Tyr–His residue in the active site of cytochrome c oxidase (CcO). The dihedral angle between the cresol and imidazole moieties is 42.21 (4)°, which is similar to that of the tyrosine‐linked histidine in bovine heart CcO. In the title compound, the R and S enantiomers of axial chirality are connected by an O—H⋯N hydrogen bond.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.