Kinetic Analysis of H2O2 Activation by an Iron(III) Complex in Water Reveals a Nonhomolytic Generation Pathway to an Iron(IV)oxo Complex

CJ Miller, Y Chang, C Wegeberg, CJ McKenzie… - ACS …, 2021 - ACS Publications
[FeIII (OH)(tpena)]+(tpena–= N, N, N′-tris (2-pyridylmethyl) ethylenediamine-N′-acetate)
catalytically activates H2O2 with the concomitant formation of the active oxidants [FeIV …

Iron-Catalyzed Synthesis of Peroxylpyrrolo[2,1-a]isoquinolines through Oxidative Dearomatization

X Huang, AN Yu, D Yang, X Gao, ST Liang… - The Journal of …, 2023 - ACS Publications
A mild late-stage modification of pyrrolo [2, 1-a] isoquinolines was established through iron-
catalyzed oxidative dearomatization and peroxidation. Peroxylated pyrroloisoquinolines …

Remote amino acid recognition enables effective hydrogen peroxide activation at a manganese oxidation catalyst

L Vicens, G Olivo, M Costas - … Chemie International Edition, 2022 - Wiley Online Library
Precise delivery of a proton plays a key role in O2 activation at iron oxygenases, enabling
the crucial O− O cleavage step that generates the oxidizing high‐valent metal–oxo species …

Oxidation of sulfur compounds by oxo-Re (V) complexes containing salophen ligands through radical pathway

H Il, I Gumus - Polyhedron, 2023 - Elsevier
Oxidation, which converts sulfides into sulfoxides, is a widely used method for producing
synthetic intermediates in various industries such as chemical, medicinal chemistry, and …

O−O Bond Formation and Liberation of Dioxygen Mediated by N5‐Coordinate Non‐Heme Iron(IV) Complexes

N Kroll, I Speckmann, M Schoknecht… - Angewandte …, 2019 - Wiley Online Library
Formation of the O− O bond is considered the critical step in oxidative water cleavage to
produce dioxygen. High‐valent metal complexes with terminal oxo (oxido) ligands are …

Manganese (II) Porphyrin and Cumyl Hydroperoxide: An Efficient Catalyst for Aryl‐Pentazole C− N Bond Cleavage

F Zhao, L Chen, X Chen, B Song, P Gao… - … A European Journal, 2025 - Wiley Online Library
The selective cleavage of C− N bonds in N‐containing compounds holds significant
research value in organic synthesis, particularly for the synthesis of promising polynitrogen …

Disproportionation of H2O2 to Dioxygen on a Nonheme Iron Center. A Computational Study

HPH Wong, F Banse, SP de Visser - ChemCatChem, 2023 - Wiley Online Library
Hydrogen peroxide is a versatile reductant that under the right conditions can react to form
dioxygen in an electrochemical reaction. This reaction has a low carbon footprint and …

Cooperative Co-Activation of Water and Hypochlorite by a Non-Heme Diiron (III) Complex

JN McPherson, CJ Miller, C Wegeberg… - Journal of the …, 2021 - ACS Publications
Aqueous solutions of the iron (III) complex of N, N, N′-tris (2-pyridylmethyl)
ethylenediamine-N′-acetate (tpena) react with hypochlorite (ClO–) to produce the reactive …

Preparation of organocobalt (iii) complexes via O 2 activation

MS Møller, J Kongsted, CJ McKenzie - Dalton Transactions, 2021 - pubs.rsc.org
The coupling of selective C–H activation with O2 activation is an important goal for organic
synthesis. New experimental and computational results, along with the results from …

Biomimetic aerobic epoxidation of alkenes catalyzed by cobalt porphyrin under ambient conditions in the presence of sunflower seeds oil as a co-substrate

J Jiang, HY Chen, XT Zhou, YJ Chen, C Xue, HB Ji - ACS omega, 2020 - ACS Publications
In this work, a mild and sustainable catalytic aerobic epoxidation of alkenes catalyzed by
cobalt porphyrin was performed in the presence of sunflower seeds oil. Under ambient …