High valent iron-oxo species are often invoked as the key oxidizing agents in the catalytic cycles of oxygen activating nonheme iron enzymes, and three of these intermediates have in fact been characterized. To gain further insight into such species, a number of biomimetic complexes have been designed and investigated as functional models for these enzymes. Progress since 2000 is summarized in this review. Many of the model complexes discussed in this review carry out oxidative transformations of relevance to the enzymatic reactions; however, the participation of a high-valent iron-oxo species (Fe(IV)O or Fe(V)O) can only be inferred. Arguments in support of a metal-based oxidant (rather than an oxygen radical species) usually hinge on the high conversion for the transformation and the nature of the reaction products, as well as the incorporation of label into these products from H(2)(18)O or related species. Within this time period, the first bona fide nonheme Fe(IV)O complexes have been generated and identified spectroscopically, three of which are crystallographically characterized. Taken together, these studies emphasize the important role the supporting polydentate ligand plays in eliciting the desired high-valent iron-oxo chemistry.
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http://dx.doi.org/10.1016/j.jinorgbio.2006.01.014 | DOI Listing |
J Phys Chem B
January 2025
Department of Chemistry and Biochemistry, Thapar Institute of Engineering and Technology, Patiala 147001, Punjab, India.
This study presents a detailed density functional theory (DFT) investigation into the mechanism and energetics of C-H activations catalyzed by bioinspired Fe(IV)O complexes, particularly in the presence of -hydroxy mediators. The findings show that these mediators significantly enhance the reactivity of the iron-oxo complex. The study examines three substrates with varying bond dissociation energies─ethylbenzene, cyclohexane, and cyclohexadiene─alongside the [Fe(IV)O(N4Py)] complex.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, Chengdu, Sichuan 610065, China; School of Architecture and Environment, Sichuan University, Chengdu 610065, China. Electronic address:
Selective oxidation relying on high-valent iron-oxo species (Fe(IV/V)) is a promising way of effective organic decontamination. However, Fe(IV/V) formation and further purposeful reinforcement production are commonly insufficient and unsustainable. Herein, cerium (Ce) modification strategy was adopted for efficient micropollutants removal through boosting Fe(IV/V) generation.
View Article and Find Full Text PDFEnviron Sci Technol
December 2024
Department of Environmental Science and Engineering, School of Architecture and Environment, Sichuan University, Chengdu 610065, China.
Advanced oxidation processes (AOPs) based on peracetic acid (PAA) offer a promising strategy to address antibiotic wastewater pollution. In this study, Fe-doped graphitic carbon nitride (g-CN) nanomaterials were used to construct Fe-N sites, and the electronic structure was tuned by boron nitride quantum dots (BNQDs), thereby optimizing PAA activation for the degradation of antibiotics. The BNQDs-modified Fe-doped g-CN catalyst (BNQDs-FCN) achieved an excellent reaction rate constant of 0.
View Article and Find Full Text PDFWater Res
January 2025
School of Environment, Henan Normal University, Key Laboratory of Yellow River and Huai River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, International Joint Laboratory on Key Techniques in Water Treatment, Henan Province, Henan Engineering Laboratory of Environmental Functional Materials and Pollution Control, Xinxiang, Henan 453007, PR China.
The application of Fe-catalyzed periodate (PI) processes is often limited by both the narrow applicable pH range and weak reaction between Fe(III) and oxidant. Here, the biodegradable picolinic acid (PICA) was used as one kind of chelating ligands (CLs) to enhance the removal of organic pollutants (OPs) at initial pH 3.0-8.
View Article and Find Full Text PDFInorg Chem
November 2024
School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A & 2B Raja S. C. Mullick Road, Kolkata, Jadavpur 700032, India.
Two mononuclear iron(II) complexes, [(6-amide-BPMEN)Fe](OTf) () and [(6-amide-Me-BPMEN)Fe(OTf)](OTf) (), supported by two BPMEN-derived (BPMEN = ,-dimethyl-,-bis(pyridine-2-yl-methyl)ethane-1,2-diamine) ligands bearing one or two amide functionalities have been isolated to study their reactivity in the oxygenation of C-H and C═C bonds using isopropyl 2-iodoxybenzoate (Pr-IBX ester) as the oxidant. Both and contain six-coordinate high-spin iron(II) centers in the solid state and in solution. The 6-amide-BPMEN ligand stabilizes an = 1 iron(IV)-oxo intermediate, [(6-amide-BPMEN)Fe(O)] ().
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