November 8, 2012
Journal Article

Distant protonated pyridine groups in water-soluble iron porphyrin
electrocatalysts promote selective oxygen reduction to water

Abstract

Fe(III)-meso-tetra(pyridyl)porphines are selective electrocatalysts for the reduction of dioxygen to water in aqueous acidic solution. The 2-pyridyl derivatives, both the triflate and chloride salts, are more selective than the isomeric 4-pyridyl complexes. The improved selectivity of is ascribed to the inward-pointing pyridinium groups acting as intramolecular proton relays. This research was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science. Pacific Northwest National Laboratory is operated by Battelle for the US Department of Energy.

Revised: November 12, 2012 | Published: November 8, 2012

Citation

Matson B.D., C.T. Carver, A.L. Von Ruden, J.Y. Yang, S. Raugei, and J.M. Mayer. 2012. "Distant protonated pyridine groups in water-soluble iron porphyrin electrocatalysts promote selective oxygen reduction to water." Chemical Communications 48, no. 90:11100-11102. PNNL-SA-89163. doi:10.1039/c2cc35576k