Catalytic oxidation of nitric oxide and nitrite mediated by water-soluble high-valent iron porphyrins at an ITO electrode

A stepwise catalytic oxidation for nitric oxide and nitrite by water-soluble iron(III) meso-tetrakis(N -methylpyridinium-4yl)porphyrin (Fe(4-TMPyP)) was first revealed by using an ITO electrode. Electrochemical and spectroelectrochemical studies characterized the formation of oxoiron(IV) porphyrin and oxoiron(IV) porphyrin p-cation radical in the oxidation of Fe(4TMPyP). O@Fe(4-TMPyP) showed selective catalytic oxidation towards NO against NO 2 with a normalized catalytic current of 3.4. The electrogenerated O@Fe(4-TMPyP) p-cation radical effectively catalyzed the oxidation of NO 2 to NO 3 via nitrogen dioxide ( NO2) intermediate. Product analysis clarified that nitrite was the sole product in the catalytic oxidation of NO by O@Fe(4-TMPyP) electrogenerated at 0.85 V vs. AgjAgCl, but nitrate was the final product after electrolysis at 1.1 V vs. AgjAgCl. The different chemical reactivities of high-valent iron porphyrins electrogenerated at the separated potentials indicated the possibility of selective electrochemical detection of NO. A mechanism of typical chemical catalysis was proposed for the catalytic oxidations of NO and NO 2 by oxoiron(IV) porphyrin complexes. 2004 Elsevier B.V. All rights reserved.