Work

Localized Cation Unlocks Unique Activity-Selectivity Trends in Molecular Oxygen Reduction Catalysis

Year: 2026

Type: article

Abstract: Integrating electrostatic and Lewis acid effects within a single molecular framework is a critically designed consideration central to the rational design of functional catalysts. Here, we report modular crown–porphyrin architectures that incorporate redox-inactive cations into programmable secondary coordination environments. This design enables systematic modulation of local electric fields, revealing charge-dependent perturbations across mono-, di-, and tri-valent cations through spectroscopic and electrochemical analyses. In oxygen reduction catalysis, the corresponding iron complexes ( FeL1–Cl ) display tunable reactivity landscapes arising from the interplay of electrostatic and Lewis acid effects. These results provide a framework for the design of cation-responsive molecular architectures in which cooperative noncovalent interactions can be leveraged to influence catalytic outcomes, as illustrated here for oxygen reduction reaction.

Source: Journal of the American Chemical Society

DOI: 10.1021/jacs.5c18246