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Kinetic behavior and thermochemical properties of phenoxy radicals
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112077zenodo-depositor-declared
From phenols to quinones: Thermodynamics of radical scavenging activity of para-substituted phenols
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Equilibrium acidities and homolytic bond dissociation enthalpies ofm- andp-substituted benzaldoximes and phenyl methyl ketoximes
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0292openalex-snapshot
Transient Phenoxyl Radicals: Formation and Properties in Aqueous Solutions
inferred← citeshttps://doi.org/10.1002/9781119953678.rad055openalex-snapshot
Antioxidants in Chemistry and Biology
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Zur möglichen Rolle des protonengekoppelten Elektronentransfers (PCET) bei der Oxidation von Wasser durch das Photosystem II
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The Possible Role of Proton‐Coupled Electron Transfer (PCET) in Water Oxidation by Photosystem II
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Mechanism of the Hydrogen Transfer from the OH Group to Oxygen‐Centered Radicals: Proton‐Coupled Electron‐Transfer versus Radical Hydrogen Abstraction
inferred← citeshttps://doi.org/10.1002/chin.197542077openalex-snapshot
ChemInform Abstract: THE KINETIC BEHAVIOR AND THERMOCHEMICAL PROPERTIES OF PHENOXY RADICALS
inferred← citeshttps://doi.org/10.1002/cphc.200900387openalex-snapshot
Different Catalytic Effects of a Single Water Molecule: The Gas‐Phase Reaction of Formic Acid with Hydroxyl Radical in Water Vapor
inferred← citeshttps://doi.org/10.1002/hlca.200690208openalex-snapshot
Reactions of Alkyl Radicals with Substituted Toluenes and the Effect of Substituents on Dissociation Energies of Benzyl CH Bonds
inferred← citeshttps://doi.org/10.1002/kin.10075openalex-snapshot
Bond dissociation energies and the Hammett correlation, Part 1: Remotely substituted aromatic compounds and vitamin E
inferred← citeshttps://doi.org/10.1002/kin.550090202openalex-snapshot
The very low‐pressure pyrolysis of phenyl ethyl ether, phenyl allyl ether, and benzyl methyl ether and the enthalpy of formation of the phenoxy radical
inferred← citeshttps://doi.org/10.1002/kin.550120302openalex-snapshot
Effect of solvent viscosity on the kinetics of reversible dimerization of phenoxy radicals
inferred← citeshttps://doi.org/10.1002/kin.550170304openalex-snapshot
On the interaction of hydroperoxide and inhibitor molecules
inferred← citeshttps://doi.org/10.1002/kin.550200908openalex-snapshot
ESR equilibrium measurements of the OH bond energy in α‐tocopherol
inferred← citeshttps://doi.org/10.1002/kin.550210809openalex-snapshot
Unusual selectivities of radical reactions. Experimental studies on alkyl versus phenoxyl reaction systems
inferred← citeshttps://doi.org/10.1002/pen.23167openalex-snapshot
Electron‐beam deposition of polyethylene composite coatings at various initiators and inhibitors
inferred← citeshttps://doi.org/10.1002/poc.725openalex-snapshot
Solvation effects of H2O and DMSO on the O—H bond dissociation energies of substituted phenols
inferred← citeshttps://doi.org/10.1002/qua.21522openalex-snapshot
Substituent effects on O–H and S–H bond dissociation enthalpies of disubstituted phenols and thiophenols
inferred← citeshttps://doi.org/10.1002/qua.560380217openalex-snapshot
MNDO calculation of reaction heats determininig the mechanism of antioxidant action of the phenols in polyolefins
inferred← citeshttps://doi.org/10.1006/abbi.2001.2431openalex-snapshot
Absolute Kinetic Characterization of 17-β-Estradiol as a Radical-Scavenging, Antioxidant Synergist
inferred← citeshttps://doi.org/10.1007/10201381_24openalex-snapshot
8.3.1.4 Reactions involving a different radical
inferred← citeshttps://doi.org/10.1007/10201381_26openalex-snapshot
8.3.3.1 Reactions of phenoxyl radicals with hydrocarbons
inferred← citeshttps://doi.org/10.1007/10201381_27openalex-snapshot
8.3.3.2 Reactions of phenoxyl radicals with alcohols
inferred← citeshttps://doi.org/10.1007/10201381_28openalex-snapshot
8.3.3.4 Reactions of phenoxyl radicals with hydroperoxides
inferred← citeshttps://doi.org/10.1007/10201381_29openalex-snapshot
8.3.3.5 Reactions of phenoxyl radicals with peroxides
inferred← citeshttps://doi.org/10.1007/10201381_30openalex-snapshot
8.3.3.6 Reactions of phenoxyl radicals with phenols
inferred← citeshttps://doi.org/10.1007/10201381_50openalex-snapshot
8.5.1.3 Reactions involving a different radical
inferred← citeshttps://doi.org/10.1007/978-1-4684-5568-7_15openalex-snapshot
Homolysis of Substituted Anisoles: Substituent Effects on Phenoxyl Radical Stabilities
inferred← citeshttps://doi.org/10.1007/978-1-4899-2034-8_2openalex-snapshot
Electrochemical Applications in Organic Chemistry
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Chemical and Photo Oxidation
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Bedeutung und Wirkungsweise von Antioxidanzien
inferred← citeshttps://doi.org/10.1007/978-94-009-3781-9_31openalex-snapshot
The Effect of Structure and Solvation on the Thermodynamic Parameters for the Formation of Singly and Doubly Charged Ions of Organic Compounds in Solution
inferred← citeshttps://doi.org/10.1007/bf00713594openalex-snapshot
Negative activation energies and compensation effects for the reactions of diarylaminyl radicals with phenols
inferred← citeshttps://doi.org/10.1007/bf00779133openalex-snapshot
Antioxidant activity and synergism of butylhydroxytoluene in processes of oxidation of retinol esters
inferred← citeshttps://doi.org/10.1007/bf00961741openalex-snapshot
Flash photolysis study of the kinetics of the destruction of mono- and disubstituted phenoxyl radicals
inferred← citeshttps://doi.org/10.1007/bf01372466openalex-snapshot
Theoretical investigation of mechanism of antioxidant action of sterically hindered phenols
inferred← citeshttps://doi.org/10.1007/bf02802036openalex-snapshot
Synergistic antioxidant effect of nucleic acids and tocopherols
inferred← citeshttps://doi.org/10.1016/0009-2614(83)87223-6openalex-snapshot
Temperature dependence of cage processes in the photofragmentation of phenyl acetate
inferred← citeshttps://doi.org/10.1016/0014-5793(89)80889-0openalex-snapshot
Correlation between the OH bond dissociation energies of ellipticine hydroxylated derivatives and their cytotoxic properties
inferred← citeshttps://doi.org/10.1016/0016-2361(84)90150-9openalex-snapshot
Reactions of methylene and ether bridges
inferred← citeshttps://doi.org/10.1016/0032-3950(82)90264-7openalex-snapshot
Sterically hindered phenols—antioxidants for polyolefines. Relation of antioxidative activity to structure. Review
inferred← citeshttps://doi.org/10.1016/0040-4020(84)85061-9openalex-snapshot
Model compound studies related to peroxidases-II
inferred← citeshttps://doi.org/10.1016/0079-6700(92)90011-mopenalex-snapshot
New dual parameters for radical reactivities of vinyl monomers
inferred← citeshttps://doi.org/10.1016/0166-1280(88)80046-0openalex-snapshot
Ab initio MO calculations of molecular structure and reactivity of the phenoxy radical
inferred← citeshttps://doi.org/10.1016/0167-4838(91)90529-9openalex-snapshot
Identification of a globin free radical in equine myoglobin treated with peroxides
inferred← citeshttps://doi.org/10.1016/0167-4838(93)90002-9openalex-snapshot
Detection and reactions of the globin radical in haemoglobin
inferred← citeshttps://doi.org/10.1016/1010-6030(94)04031-vopenalex-snapshot
Laser photolysis study of naphthalene disulphides and naphthalene thiols; reactivities of naphthalenethio radicals
inferred← citeshttps://doi.org/10.1016/j.chemphys.2005.03.001openalex-snapshot
Mechanisms of antioxidant activity: The DFT study of hydrogen abstraction from phenol and toluene by the hydroperoxyl radical
inferred← citeshttps://doi.org/10.1016/j.chemphys.2005.06.011openalex-snapshot
Theoretical study of deuterium kinetic isotope effect in peroxidation of phenol and toluene
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.134866openalex-snapshot
Kinetic modeling of the reversal of antioxidant potency of α-, β-, γ- and δ-tocopherols in methyl linoleate peroxidation
inferred← citeshttps://doi.org/10.1016/j.jmgm.2025.108959openalex-snapshot
O-H/N-H bond dissociation energies in 1,4-hydroquinone, 4-hydroxydiphenylamine, N,N′-diphenyl-1,4-phenylenediamine, and their phenoxyl and aminyl radicals
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A determination of antioxidant efficiencies using ESR and computational methods
inferred← citeshttps://doi.org/10.1016/s0005-2728(00)00069-4openalex-snapshot
Proton and hydrogen currents in photosynthetic water oxidation
inferred← citeshttps://doi.org/10.1016/s0006-291x(03)00810-6openalex-snapshot
Radical–radical reactions of superoxide: a potential route to toxicity
inferred← citeshttps://doi.org/10.1016/s0009-2614(01)00892-2openalex-snapshot
Empirical valence bond study of radical reactions: hydrogen atom transfer in peroxidation of phenol
inferred← citeshttps://doi.org/10.1016/s0021-9258(17)32375-xopenalex-snapshot
On the mechanism of the nitric oxide synthase-catalyzed conversion of N omega-hydroxyl-L-arginine to citrulline and nitric oxide.
inferred← citeshttps://doi.org/10.1016/s0021-9258(19)70741-8openalex-snapshot
A carbon-centered free radical intermediate in the prostaglandin synthetase oxidation of arachidonic acid. Spin trapping and oxygen uptake studies.
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)81645-8openalex-snapshot
On the regioselectivity of the fremy's salt oxidation of phenols
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)91485-1openalex-snapshot
MNDO calculations of the effects of substitution on antioxidant activity of phenols and Vitamin E
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88462-2openalex-snapshot
Enynones in organic synthesis. II. An electron transfer mediated synthesis of methylenecyclopentenones
inferred← citeshttps://doi.org/10.1016/s0069-8040(08)70036-0openalex-snapshot
Chapter 1 Kinetics and Mechanisms of Free Radical Oxidation of Alkanes and Olefins in the Liquid Phase
inferred← citeshttps://doi.org/10.1016/s0082-0784(06)80718-6openalex-snapshot
Reactions of phenoxy radicals in the gas phase
inferred← citeshttps://doi.org/10.1016/s1367-5931(98)80066-5openalex-snapshot
Manganese and tyrosyl radical function in photosynthetic oxygen evolution
inferred← citeshttps://doi.org/10.1016/s1369-5266(00)80071-0openalex-snapshot
Concerted hydrogen-atom abstraction in photosynthetic water oxidation
inferred← citeshttps://doi.org/10.1021/acs.jced.5b00402openalex-snapshot
Thermodynamic Parameters Including Acid Dissociation Constants for Bromochlorophenols (BCPs)
inferred← citeshttps://doi.org/10.1021/ar50151a001openalex-snapshot
Electron paramagnetic resonance and the art of physical-organic chemistry
inferred← citeshttps://doi.org/10.1021/ar9600188openalex-snapshot
Oxygen Production in Nature: A Light-Driven Metalloradical Enzyme Process
inferred← citeshttps://doi.org/10.1021/bi0018077openalex-snapshot
Effects of Sr 2+ -Substitution on the Reduction Rates of Y z • in PSII MembranesEvidence for Concerted Hydrogen-Atom Transfer in Oxygen Evolution
inferred← citeshttps://doi.org/10.1021/bi301613popenalex-snapshot
Reversible Phenol Oxidation and Reduction in the Structurally Well-Defined 2-Mercaptophenol-α3C Protein
inferred← citeshttps://doi.org/10.1021/cr9601021openalex-snapshot
Comparative QSAR: Radical Reactions of Benzene Derivatives in Chemistry and Biology
inferred← citeshttps://doi.org/10.1021/ja004081aopenalex-snapshot
Oxygen−Carbon Bond Dissociation Enthalpies of Benzyl Phenyl Ethers and Anisoles. An Example of Temperature Dependent Substituent Effects 1
inferred← citeshttps://doi.org/10.1021/ja026289xopenalex-snapshot
Substituent Effects on the Bond Dissociation Enthalpies of Aromatic Amines
inferred← citeshttps://doi.org/10.1021/ja0500409openalex-snapshot
A Theoretical Study of the Iminoxyl/Oxime Self-Exchange Reaction. A Five-Center, Cyclic Proton-Coupled Electron Transfer
inferred← citeshttps://doi.org/10.1021/ja503348dopenalex-snapshot
Photochemical Tyrosine Oxidation in the Structurally Well-Defined α3Y Protein: Proton-Coupled Electron Transfer and a Long-Lived Tyrosine Radical
inferred← citeshttps://doi.org/10.1021/ja961469qopenalex-snapshot
Solvent Effects on Homolytic Bond Dissociation Energies of Hydroxylic Acids
inferred← citeshttps://doi.org/10.1021/ja962931+openalex-snapshot
A Computational Analysis of Substituent Effects on the O−H Bond Dissociation Energy in Phenols: Polar Versus Radical Effects
inferred← citeshttps://doi.org/10.1021/ja963378zopenalex-snapshot
Theoretical Calculation of Substituent Effects on the O−H Bond Strength of Phenolic Antioxidants Related to Vitamin E
inferred← citeshttps://doi.org/10.1021/jo026501fopenalex-snapshot
A Quantitative Approach to the Recycling of α-Tocopherol by Coantioxidants
inferred← citeshttps://doi.org/10.1021/jo034094hopenalex-snapshot
Remote Substituent Effects on Homolytic Bond Dissociation Energies
inferred← citeshttps://doi.org/10.1021/jo0348017openalex-snapshot
Kinetic Study of the Phthalimide N-Oxyl Radical in Acetic Acid. Hydrogen Abstraction from Substituted Toluenes, Benzaldehydes, and Benzyl Alcohols
inferred← citeshttps://doi.org/10.1021/jo0351825openalex-snapshot
Modeling the Co-Antioxidant Behavior of Monofunctional Phenols. Applications to Some Relevant Compounds
inferred← citeshttps://doi.org/10.1021/jo801501eopenalex-snapshot
A Simple Cu-Catalyzed Coupling Approach to Substituted 3-Pyridinol and 5-Pyrimidinol Antioxidants
inferred← citeshttps://doi.org/10.1021/jo952167uopenalex-snapshot
Application of Photoacoustic Calorimetry to the Measurement of the O−H Bond Strength in Vitamin E (α- and δ-Tocopherol) and Related Phenolic Antioxidants1
inferred← citeshttps://doi.org/10.1021/jo960069iopenalex-snapshot
A Density Functional Study of Substituent Effects on the O−H and O−CH3 Bond Dissociation Energies in Phenol and Anisole
inferred← citeshttps://doi.org/10.1021/jo961039iopenalex-snapshot
Bond Dissociation Energies of O−H Bonds in Substituted Phenols from Equilibration Studies
inferred← citeshttps://doi.org/10.1021/jp012396mopenalex-snapshot
A Theory that Connects Proton-Coupled Electron-Transfer and Hydrogen-Atom Transfer Reactions
inferred← citeshttps://doi.org/10.1021/jp0155359openalex-snapshot
Comment on “Identity Hydrogen Abstraction Reactions, X• + H−X‘ → X−H + X‘• (X = X‘ = CH3, SiH3, GeH3, SnH3, PbH3): A Valence Bond Modeling”
inferred← citeshttps://doi.org/10.1021/jp035927aopenalex-snapshot
The Trapping of the OH Radical by Coenzyme Q. A Theoretical and Experimental Study
inferred← citeshttps://doi.org/10.1021/jp073515mopenalex-snapshot
Energetics of Cresols and of Methylphenoxyl Radicals
inferred← citeshttps://doi.org/10.1021/jp902354aopenalex-snapshot
Effects of Molecule Stabilization Energies on Radical Reactions: G3 and G3(MP2) Model Chemistries Applied to Benzylic Systems
inferred← citeshttps://doi.org/10.1021/jp911137popenalex-snapshot
Thermodynamic Diagnosis of the Properties and Mechanism of Dihydropyridine-Type Compounds as Hydride Source in Acetonitrile with “Molecule ID Card”
inferred← citeshttps://doi.org/10.1021/jp9704325openalex-snapshot
Carbon−Oxygen Bond Strength in Diphenyl Ether and Phenyl Vinyl Ether: An Experimental and Computational Study
inferred← citeshttps://doi.org/10.1021/jp982321ropenalex-snapshot
A Quantum Chemical Study of the Mechanism of Tyrosinase
inferred← citeshttps://doi.org/10.1021/ol0261837openalex-snapshot
Hydrogen Bonding between Phenols and Fatty Acid Esters: 1H NMR Study and ab Initio Calculations
inferred← citeshttps://doi.org/10.1023/a:1016600727116openalex-snapshot
Standard Enthalpies of Formation of 2,6-Di-tert-butyl4-methylphenol and 3,5-Di-tert-butylphenol and Their Phenoxy Radicals
inferred← citeshttps://doi.org/10.1023/a:1022576802859openalex-snapshot
Determination of the Kinetic Significance of Elementary Steps in the Reaction of Ethylbenzene Oxidation Inhibited by para-Substituted Phenols: Choice of an Effective Antioxidant
inferred← citeshttps://doi.org/10.1023/a:1024406128668openalex-snapshot
Determination by the EPR Radical Equilibration Technique of the O–H Bond Dissociation Enthalpy in 3,5-Dimethylphenol
inferred← citeshttps://doi.org/10.1039/b901838gopenalex-snapshot
Free radical intermediates in the inhibition of the autoxidation reaction
inferred← citeshttps://doi.org/10.1039/c39920000967openalex-snapshot
Phenol–phenoxyl radical equilibria by electron spin resonance: are radicals derived from tocopherol and analogues exceptionally stabilized?
inferred← citeshttps://doi.org/10.1039/c3ob40831kopenalex-snapshot
A classical but new kinetic equation for hydride transfer reactions
inferred← citeshttps://doi.org/10.1039/p29940000785openalex-snapshot
Entropic and enthalpic effects of 4-methoxy substitution in phenoxyl radicals
inferred← citeshttps://doi.org/10.1039/p29960000649openalex-snapshot
Stereoselectivity and mechanism in the electrohydrodimerisation of esters of cinnamic acid
inferred← citeshttps://doi.org/10.1046/j.1365-3075.1999.00279.xopenalex-snapshot
Substituent effects on the O-H bond dissociation enthalpies in phenolic compounds: agreements and controversies
inferred← citeshttps://doi.org/10.1063/1.467220openalex-snapshot
Structure and fundamental vibrations of phenoxyl radical
inferred← citeshttps://doi.org/10.1070/rc1981v050n10abeh002719openalex-snapshot
Chemical and Biological Kinetics
inferred← citeshttps://doi.org/10.1070/rc2005v074n09abeh001177openalex-snapshot
Estimation of the bond dissociation energies from the kinetic characteristics of liquid-phase radical reactions
inferred← citeshttps://doi.org/10.1073/pnas.1112057109openalex-snapshot
Reversible voltammograms and a Pourbaix diagram for a protein tyrosine radical
inferred← citeshttps://doi.org/10.1080/05698197908982928openalex-snapshot
The Effects of Antioxidant Reactions on the Wear Behavior of a Zinc Dialkyldithiophosphate
inferred← citeshttps://doi.org/10.1080/09553008714551871openalex-snapshot
Reactions of Linoleic Acid Peroxyl Radicals with Phenolic Antioxidants: A Pulse Radiolysis Study
inferred← citeshttps://doi.org/10.1080/10426509108038090openalex-snapshot
SULFENAMIDES AND SULFINAMIDES VII. REACTIONS OF ARYL SULFINAMIDES WITH DIPHENYLPICRYLHYDRAZYL FREE RADICAL
inferred← citeshttps://doi.org/10.1098/rsos.220177openalex-snapshot
Calculating bond dissociation energies of X−H (X=C, N, O, S) bonds of aromatic systems via density functional theory: a detailed comparison of methods
inferred← citeshttps://doi.org/10.1134/s0023158416010067openalex-snapshot
Homodesmotic method of determining the O–H bond dissociation energies in phenols
inferred← citeshttps://doi.org/10.1179/1351000212y.0000000030openalex-snapshot
Computation of the bond dissociation enthalpies and free energies of hydroxylic antioxidants using theab initioHartree–Fock method
inferred← citeshttps://doi.org/10.1201/9781420030853.pt2openalex-snapshot
Heterogeneous Inhibition of Oxidation
inferred← citeshttps://doi.org/10.1246/bcsj.20120265openalex-snapshot
Theoretical Study of the Substituent and Solvent Effects on the Reaction Enthalpies of the Antioxidant Mechanisms of Tyrosol Derivatives
inferred← citeshttps://doi.org/10.1351/pac199971071249openalex-snapshot
Substituent effects on the O–H bond dissociation enthalpies in phenolic compounds: agreements and controversies + erratum
inferred← citeshttps://doi.org/10.24874/jsscm.2020.01.05openalex-snapshot
DO EQUOL’S C-RING HYDROGENS CONTRIBUTE TO FREE RADICAL SCAVENGING?
inferred← citeshttps://doi.org/10.4271/790016openalex-snapshot
The Application of Antioxidant Analysis to Transmission Fluid Testing
inferred← citeshttps://doi.org/10.5772/13290openalex-snapshot
Dissociation Energies of O−H Bonds of Phenols and Hydroperoxides
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