Five meso-substituted cobalt(III) corroles were examined as to their catalytic activity for the electoreduction of O(2) when coated on an edge-plane pyrolytic graphite electrode in 1.0 M HClO(4). The investigated compounds are represented as (TpRPCor)Co(PPh(3)), where TpRPCor is the trianion of a para-substituted triphenylcorrole and R = OMe, Me, H, F, or Cl. Three electrochemical techniques, cyclic voltammetry, linear sweep voltammetry with a rotating disk electrode (RDE), and voltammetry at a rotating ring disk electrode (RRDE), were utilized to evaluate the catalytic activity of the corroles in the reduction of O(2). Cobalt corroles containing electron-withdrawing substituents were shown to be better catalysts than those having electron-donating groups on the three meso-phenyl rings of the triarylcorroles.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ic300886sDOI Listing

Publication Analysis

Top Keywords

cobalt corroles
8
coated edge-plane
8
edge-plane pyrolytic
8
pyrolytic graphite
8
catalytic activity
8
voltammetry rotating
8
disk electrode
8
molecular oxygen
4
oxygen reduction
4
reduction electrocatalyzed
4

Similar Publications

We report herein the synthesis and full spectroscopic characterization of two AB-corrole phosphonic acids. Thanks to the presence of a phosphonic acid functional group at the 10--position, the corroles were covalently linked to the hexanuclear Zr clusters of a PCN-222 metal-organic framework (MOF). After the insertion of cobalt into the corrole macrocycle, the metal complexes are able to bind small volatile molecules such as carbon monoxide (CO).

View Article and Find Full Text PDF

Carboxyl-Group-Bearing Metal Corroles of Cobalt, Manganese and Copper for Electrocatalytic Hydrogen Evolution.

Chempluschem

January 2025

School of Chemistry and Chemical Engineering, Guangdong Provincial Key Laboratory of Fuel Cell Technology, South China University of Technology, Guangzhou, 510641, China.

Article Synopsis
  • The study focused on synthesizing 5,15-bis(perfluorophenyl)-10-(4-carboxyphenyl) corrole and its metal complexes with Co(III), Mn(III), and Cu(III) to investigate their ability to catalyze the hydrogen evolution reaction (HER).
  • Various proton sources, including AcOH, trifluoroacetic acid, and TsOH, were tested in dimethylformamide to analyze the pathways (EECC, EECEC, EEECEC) for HER based on acidity and concentration.
  • Among the complexes, the Co corrole exhibited the highest efficiency with a turnover frequency of 201 s, showing the catalytic activity ranking as Co > Cu > Mn in
View Article and Find Full Text PDF

Considering the potential advantages of minimally sized corroles for diverse applications, this study reports a facile access to cyano-substituted derivatives via a rare CF/CN conversion. Investigation of the fully characterized gallium, phosphorus, and cobalt complexes discloses multiple effects of the meso-nitrile groups attached to the macrocycle. This corrole appears to be the most electron poor derivative which comes into play in the redox potentials of the corresponding complexes.

View Article and Find Full Text PDF

CoCorrole-Functionalized PCN-222 for Carbon Monoxide Selective Adsorption.

Chemistry

September 2024

Institut de Chimie Moléculaire de l'Université de Bourgogne, ICMUB, UMR CNRS 6302, Université de Bourgogne, 9, Avenue Alain Savary, BP 47870, 21078, Dijon Cedex, France.

The high risk of CO poisoning justifies the need for indoor air quality control and warning systems based on the detection of low concentrations (ppm-ppb) of CO. Cobalt corrole complexes selectively bind CO vs. O, CO, N, opening new fields of applications.

View Article and Find Full Text PDF

The strong two-photon induced nonlinear absorption and self-focusing type positive nonlinear refraction are pronounced by the structural engineering in β-functionalized cobalt corroles.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!