Polarized Bimetallic Site Synergy in Ionic Structures of Cu(II), Fe(III), and Mn(III) Porphyrins: Electrochemistry and Catalytic Hydrogenation of Nitroaromatics

Abstract

Binuclear catalytic sites attained in a controlled way with complementary and cooperative metal ion centers are highly relevant in the development of new or enhanced catalytic processes. Herein, binuclear sites carrying Fe(III), Cu(II), or Mn(III) metal ions with a polarized structure have been prepared using the ionic selfassembly of oppositely charged metalloporphyrins. Binary porphyrin structures (BIPOS) have been prepared based on metalloporphyrin cations carrying pyridinium or methylpyridinium groups in conjugation with metalloporphyrin anions carrying sulfonatophenyl groups. BIPOS carrying [cation/anion] tecton pairs of [Cu/Fe], [Fe/Cu], [Cu/Cu], [Fe/Fe], [Mn/Fe], [Fe/Mn], and [Mn/Mn] have been compared. Electrochemical interaction and enhanced catalytic behavior are noticeable for BIPOS [Fe/Cu], [Fe/Fe], and [Mn/Fe] carrying a Fe center and [less electronegative/more electronegative] metal ion centers in the [cation/anion] porphyrin ionic pairs. For high-performance BIPOS, cyclic voltammograms showed a greater separation of the cathodic and anodic peaks, within ΔE p = 0.095−0.125 V, and the rate constants for the catalytic reduction of 4-nitrophenol were within k = 0.380−0.535 min −1 /mg of catalyst, significantly superior to the related individual metalloporphyrins. Inverse heterobimetallic [Cu/Fe] and [Fe/ Mn] and the homometallic BIPOS [Cu/Cu] and [Mn/Mn] were significantly less active or inefficient. A [Fe/Cu] material could be reused in at least 5 catalytic cycles, maintaining catalytic activity; the best catalysts were also active in the reduction of nitrobenzene to aniline in mild conditions (visible light, 30 °C, 0.5 mol % catalyst), and an [Fe/Fe] catalyst showed 100% aniline yield after 2 h.