Highly oxidized metals are constituents of oxidants, reactive intermediates, and materials with interesting conductive and magnetic properties. High-energy spectroscopies have played an important role in identifying and describing the bonding character of highly oxidized metals in these materials. A systematic study of Cu(III) K-edge X-ray absorption spectra was carried out to identify analytically useful signatures of Cu(III) in the K-edge, and to elucidate bonding descriptions for Cu(III)-containing complexes. K-edges for six Cu(III) complexes and their same-ligand Cu(II) counterparts are compared. Edges for the Cu(III) species generally appear at higher energies than their Cu(II) counterparts, though energy shifts between most individual edge features vary. However, for all Cu(III) compounds studied, the 1s f 3d transition in the preedge energy range exhibits a distinct, 2 eV shift to higher energy, relative to the known and relatively unvarying energy of the 1s f 3d transition in Cu(II) species. This energy shift provides a direct means of distinguishing Cu(III) from Cu(II). The K-edge for a complex containing Cu(II) coordinated to a 1e --oxidized ligand (phenoxyl) does not show such a change in the 1s f 3d transition energy. The analytical potential of the Cu K-edge was tested with good success using a mixed-valent trinuclear species. Cu(III) is detectable using the K-edge. The limitations of the K-edge as a Cu(III) analytical probe are discussed. An analysis applied to the 1s f 4p and 1s f 4p + shakedown transitions in the edge for a {Cu II 2 (µ-OH) 2 } 2+ dimer, using a configurational interaction (CI) model, predicted ∼75% d-character in the ground state. A similar analysis of the K-edge for {Cu III 2 (µ-O) 2 } 2+ indicates that the Cu in this complex has far more covalent bonds with the oxo bridging ligands (dcharacter ∼60%).

Chlorite dismutase catalyzes O2 release from chlorite with exquisite efficiency and specificity. The spectroscopic properties, ligand binding affinities, and steady state kinetics of chlorite dismutase from Dechloromonas aromatica were examined over pH 3–11.5 to gain insight into how the protonation state of the heme environment influences dioxygen formation. An acid/base transition was observed by UV/visible and resonance Raman spectroscopy with a pKa of 8.7, 2–3 pH units below analogous transitions observed in typical His-ligated peroxidases. This transition marks the conversion of a five coordinate high spin Fe(III) to a mixed high/low spin ferric-hydroxide, as confirmed by resonance Raman (rR) spectroscopy. The two Fe–OH stretching frequencies are quite low, consistent with a weak Fe–OH bond, despite the nearly neutral imidazole side chain of the proximal histidine ligand. The hydroxide is proposed to interact strongly with a distal H-bond donor, thereby weakening the Fe–OH bond. The rR spectra of Cld-CO as a function of pH reveal two forms of the complex, one in which there is minimal interaction of distal residues with the carbonyl oxygen and another, acidic form in which the oxygen is under the influence of positive charge. Recent crystallographic data reveal arginine 183 as the lone H-bond donating residue in the distal pocket. It is likely that this Arg is the strong, positively charged H-bond donor implicated by vibrational data to interact with exogenous axial heme ligands. The same Arg in its neutral (pKa ~ 6.5) form also appears to act as the active site base in binding reactions of protonated ligands, such as HCN, to ferric Cld. The steady state profile for the rate of chlorite decomposition is characterized by these same pKas. The 5 coordinate high spin acidic Cld is more active than the alkaline hydroxide-bound form. The acid form decomposes chlorite most efficiently when the distal Arg is protonated/cationic (maximum kcat = 2.0 (±0.6) × 105 s−1, kcat/KM = 3.2 (±0.4) × 107 M−1s−1, pH 5.2, 4 °C) and to a somewhat lesser extent when it acts as a H-bond donor to the axial hydroxide ligand under alkaline conditions.

Biomimetic functional models of the mononuclear copper enzyme galactose oxidase are presented that catalytically oxidize benzylic and allylic alcohols to aldehydes with O2 under mild conditions. The mechanistic fidelity between the models and the natural system is pronounced. Modest structural mimicry proves sufficient to transfer an unusual ligand-based radical mechanism, previously unprecedented outside the protein matrix, to a simple chemical system.