An Iron(III) Superoxide Corrole from Iron(II) and Dioxygen.

A new structurally characterized ferrous corrole [FeII (ttppc)]- (1) binds one equivalent of dioxygen to form [FeIII (O2-. )(ttppc)]- (2). This complex exhibits a 16/18 O2 -isotope sensitive ν(O-O) stretch at 1128 cm-1 concomitantly with a single ν(Fe-O2 ) at 555 cm-1 , indicating it is an η1 -superoxo ("end-on") iron(III) complex. Complex 2 is the first well characterized Fe-O2 corrole, and mediates the following biologically relevant oxidation reactions: dioxygenation of an indole derivative, and H-atom abstraction from an activated O-H bond.

Oxidation of an indole substrate by porphyrin iron(iii) superoxide: relevance to indoleamine and tryptophan 2,3-dioxygenases.

Reaction of FeIII(O2˙-)(TPP) with 2,3-dimethylindole at -40 °C gives the ring-opened, dioxygenated N-(2-acetyl-phenyl)-acetamide product. The reaction was monitored in situ by low-temperature UV-vis and 1H NMR spectroscopies. This work demonstrates that a discrete iron(iii)(superoxo) porphyrin is competent to carry out indole oxidation, as proposed for the tryptophan and indoleamine 2,3-dioxygenases.

The hydrogen atom transfer reactivity of a porphyrinoid cobalt superoxide complex.

The H-atom transfer (HAT) reactivity of a corrolazine cobalt superoxide with weak O-H and N-H substrates has been demonstrated. Kinetic analysis shows relatively fast rates of HAT with diphenylhydrazine (DPH). A kinetic isotope effect (KIE) and Eyring activation parameters are consistent with an HAT mechanism.

Factors Affecting Hydrogen Atom Transfer Reactivity of Metal-Oxo Porphyrinoid Complexes.

There has been considerable interest in hydrogen atom transfer (HAT) reactions mediated by metal/oxygen species because of their central role in metalloenzyme function as well as synthetic catalysts. This Account focuses on our progress in synthesizing high-valent metal-oxo and metal-hydroxo porphyrinoid complexes and determining their reactivities in a range of HAT processes. For these studies we have utilized corrolazine and corrole ligands, which are a ring-contracted subclass of porphyrinoid compounds designed to stabilize high-valent metal complexes. The high-valent manganese complex MnV(O)(TBP8Cz) (TBP8Cz = octakis(4- tert-butylphenyl)corrolazine3-) provided an early example of a well-characterized low-potential oxidant that can still be effective at abstracting H atoms from certain C-H/O-H bonds. Approximating the thermodynamics of the HAT reactivity of the MnV(O) complex and related species with the help of a square scheme approach, in which HAT can be formally separated into proton (p Ka) and electron transfers ( E°), indicates that affinity for the proton (i.e., the basicity) is a key factor in promoting HAT. Anionic axial ligands have a profound influence on the HAT reactivity of MnV(O)(TBP8Cz), supporting the conclusion that basicity is a critical parameter in determining the reactivity. The influence of Lewis acids on MnV(O)(TBP8Cz) was examined, and it was shown that both the electronic structure and reactivity toward HAT were significantly altered. High-valent Cr(O), Re(O), and Fe(O) corrolazines were prepared, and a range of HAT reactions were studied with these complexes. The chromium and manganese complexes form a rare pair of structurally characterized CrV(O) and MnV(O) species in identical ligand environments, allowing for a direct comparison of their HAT reactivities. Although the CrV(O) species was the better oxidant as measured by redox potentials, the MnV(O) species was significantly more reactive in HAT oxidations, pointing again to basicity as a key determinant of HAT reactivity. The iron complex, FeIV(O)(TBP8Cz+•), is an analogue of the heme enzyme Compound I intermediate, and was found to be mildly reactive toward H atom abstraction from C-H bonds. In contrast, ReV(O)(TBP8Cz) was inert toward HAT, although one-electron oxidation to ReV(O)(TBP8Cz+•) led to some interesting reactivity mediated by the π-radical-cation ligand alone. Other ligand modifications, including peripheral substitution as well as novel alkylation of the meso position on the Cz core, were examined for their influence on HAT. A highly sterically encumbered corrole, tris(2,4,6-triphenylphenyl)corrole (ttppc), was employed for the isolation and structural characterization of the first MnIV(OH) complex in a porphyrinoid environment, MnIV(OH)(ttppc). This complex was highly reactive in HAT with O-H substrates and was found to be much more reactive than its higher-oxidation-state counterpart MnV(O)(ttppc), providing important mechanistic insights. These studies provided fundamental knowledge on the relationship between structure and function in high-valent M(O) and M(OH) models of heme enzyme reactivity.