Photochemical Organic Oxidations and Dechlorinations with a μ-Oxo Bridged Heme/Non-Heme Diiron Complex

Steady state and laser flash photolysis studies of the heme/non-heme μ-oxo diiron complex [(⁶L)Fe^IIIOFe^IIICl]⁺ (<b>1</b>) have been undertaken. The anaerobic photolysis of benzene solutions of <b>1</b> did not result in the buildup of any photoproduct. However, the addition of excess triphenylphosphine resulted in the quantitative photoreduction of <b>1</b> to [(⁶L)Fe^II···Fe^IICl]⁺ (<b>2</b>), with concomitant production by oxo-transfer of 1 equiv of triphenylphosphine oxide. Under aerobic conditions and excess triphenylphosphine, the reaction produces multiple turnovers (∼28) before the diiron complex is degraded. The anaerobic photolysis of tetrahydrofuran (THF) or toluene solutions of <b>1</b> likewise results in the buildup of <b>2</b>. The oxidation products from these reactions included γ-butyrolactone (∼15%) for the reaction in THF and benzaldehyde (∼23%) from the reaction in toluene. In either case, the O-atom which is incorporated into the carbonyl product is derived from dioxygen present under workup or under aerobic photolysis conditions. Transient absorption measurements of low-temperature THF solutions of <b>1</b> revealed the presence of an (P)Fe^II-like {P = tetraaryl porphyrinate dianion} species suggesting that the reactive species is a formal (heme)Fe^II/Fe^IVO(non-heme) pair. The non-heme Fe^IVO is thus most likely responsible for CH bond cleavage and subsequent radical chemistry. The photolysis of <b>1</b> in chlorobenzene or 1,2-dichlorobenzene resulted in C−Cl cleavage reactions and the formation of {[(⁶L)Fe^IIICl···Fe^IIICl]₂O}²⁺ (<b>3</b>), with chloride ligands that are derived from solvent dehalogenation chemistry. The resulting organic products are biphenyl trichlorides or biphenyl monochlorides, derived from dichlorobenzene and chlorobenzene, respectively. Similarly, product <b>3</b> is obtained by the photolysis of benzene−benzyl chloride solutions of <b>1</b>; the organic product is benzaldehyde (∼70%). A brief discussion of the dehalogenation chemistry, along with relevant environmental perspectives, is included.