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Tuning the Reactivity of Cofacial Porphyrin Prisms for Oxygen Reduction Using Modular Building Blocks

Matthew R. Crawley, Daoyang Zhang, Amanda N. Oldacre, Christine M. Beavers, Alan E. Friedman, Timothy R. Cook

2020Journal of the American Chemical Society65 citationsDOI

Abstract

We assembled eight cofacial porphyrin prisms using MTPyP (M = Co(II) or Zn(II), TPyP = 4-tetrapyridylporphyrin) and functionalized ruthenium-based “molecular clips” using coordination-driven self-assembly. Our approach allows for the rapid synthesis of these architectures in isolated yields as high as 98% for the assembly step. Structural and reactivity studies provided a deeper understanding of the role of the building blocks on the oxygen reduction reaction (ORR). Catalytic efficacy was probed by using cyclic and hydrodynamic voltammetry on heterogeneous catalyst inks in aqueous media. The reported prisms showed outstanding selectivity (>98%) for the kinetically hindered 4e–/4H+ reduction of O2 to H2O over the kinetically more accessible 2e–/2H+ reduction to H2O2. Furthermore, we have demonstrated significant cofacial enhancement in the observed catalytic rate constant ks (∼5 orders of magnitude) over the mononuclear analogue. We conclude that the steric bulk of the clip plays an important role in the structural dynamics of these prisms, which in turn modulates the ORR reactivity with respect to selectivity and kinetics.

Topics & Concepts

ChemistryPorphyrinReactivity (psychology)Steric effectsCyclic voltammetrySelectivityCatalysisPhotochemistryRutheniumReaction rate constantOxygenCombinatorial chemistryKineticsElectrochemistryStereochemistryOrganic chemistryPhysical chemistryElectrodeAlternative medicineMedicineQuantum mechanicsPhysicsPathologyPorphyrin and Phthalocyanine ChemistryElectrocatalysts for Energy ConversionMetal-Catalyzed Oxygenation Mechanisms
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