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Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond.
Chem Rev. 2017 Jul 12; 117(13):9140-9162.CR

Abstract

TAML activators of peroxides are iron(III) complexes. The ligation by four deprotonated amide nitrogens in macrocyclic motifs is the signature of TAMLs where the macrocyclic structures vary considerably. TAML activators are exceptional functional replicas of the peroxidases and cytochrome P450 oxidizing enzymes. In water, they catalyze peroxide oxidation of a broad spectrum of compounds, many of which are micropollutants, compounds that produce undesired effects at low concentrations-as with the enzymes, peroxide is typically activated with near-quantitative efficiency. In nonaqueous solvents such as organic nitriles, the prototype TAML activator gave the structurally authenticated reactive iron(V)oxo units (FeVO), wherein the iron atom is two oxidation equivalents above the FeIII resting state. The iron(V) state can be achieved through the intermediacy of iron(IV) species, which are usually μ-oxo-bridged dimers (FeIVFeIV), and this allows for the reactivity of this potent reactive intermediate to be studied in stoichiometric processes. The present review is primarily focused at the mechanistic features of the oxidation by FeVO of hydrocarbons including cyclohexane. The main topic is preceded by a description of mechanisms of oxidation of thioanisoles by FeVO, because the associated studies provide valuable insight into the ability of FeVO to oxidize organic molecules. The review is opened by a summary of the interconversions between FeIII, FeIVFeIV, and FeVO species, since this information is crucial for interpreting the kinetic data. The highest reactivity in both reaction classes described belongs to FeVO. The resting state FeIII is unreactive oxidatively. Intermediate reactivity is typically found for FeIVFeIV; therefore, kinetic features for these species in interchange and oxidation processes are also reviewed. Examples of using TAML activators for C-H bond cleavage applied to fine organic synthesis conclude the review.

Authors+Show Affiliations

Department of Chemistry, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.Department of Chemistry, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213, United States.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28488444

Citation

Collins, Terrence J., and Alexander D. Ryabov. "Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond." Chemical Reviews, vol. 117, no. 13, 2017, pp. 9140-9162.
Collins TJ, Ryabov AD. Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond. Chem Rev. 2017;117(13):9140-9162.
Collins, T. J., & Ryabov, A. D. (2017). Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond. Chemical Reviews, 117(13), 9140-9162. https://doi.org/10.1021/acs.chemrev.7b00034
Collins TJ, Ryabov AD. Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond. Chem Rev. 2017 Jul 12;117(13):9140-9162. PubMed PMID: 28488444.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Targeting of High-Valent Iron-TAML Activators at Hydrocarbons and Beyond. AU - Collins,Terrence J, AU - Ryabov,Alexander D, Y1 - 2017/05/10/ PY - 2017/5/11/pubmed PY - 2017/5/11/medline PY - 2017/5/11/entrez SP - 9140 EP - 9162 JF - Chemical reviews JO - Chem Rev VL - 117 IS - 13 N2 - TAML activators of peroxides are iron(III) complexes. The ligation by four deprotonated amide nitrogens in macrocyclic motifs is the signature of TAMLs where the macrocyclic structures vary considerably. TAML activators are exceptional functional replicas of the peroxidases and cytochrome P450 oxidizing enzymes. In water, they catalyze peroxide oxidation of a broad spectrum of compounds, many of which are micropollutants, compounds that produce undesired effects at low concentrations-as with the enzymes, peroxide is typically activated with near-quantitative efficiency. In nonaqueous solvents such as organic nitriles, the prototype TAML activator gave the structurally authenticated reactive iron(V)oxo units (FeVO), wherein the iron atom is two oxidation equivalents above the FeIII resting state. The iron(V) state can be achieved through the intermediacy of iron(IV) species, which are usually μ-oxo-bridged dimers (FeIVFeIV), and this allows for the reactivity of this potent reactive intermediate to be studied in stoichiometric processes. The present review is primarily focused at the mechanistic features of the oxidation by FeVO of hydrocarbons including cyclohexane. The main topic is preceded by a description of mechanisms of oxidation of thioanisoles by FeVO, because the associated studies provide valuable insight into the ability of FeVO to oxidize organic molecules. The review is opened by a summary of the interconversions between FeIII, FeIVFeIV, and FeVO species, since this information is crucial for interpreting the kinetic data. The highest reactivity in both reaction classes described belongs to FeVO. The resting state FeIII is unreactive oxidatively. Intermediate reactivity is typically found for FeIVFeIV; therefore, kinetic features for these species in interchange and oxidation processes are also reviewed. Examples of using TAML activators for C-H bond cleavage applied to fine organic synthesis conclude the review. SN - 1520-6890 UR - https://www.unboundmedicine.com/medline/citation/28488444/Targeting_of_High_Valent_Iron_TAML_Activators_at_Hydrocarbons_and_Beyond_ L2 - https://doi.org/10.1021/acs.chemrev.7b00034 DB - PRIME DP - Unbound Medicine ER -
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