Reaction of phenols with the 2,2-diphenyl-1-picrylhydrazyl radical. Kinetics and DFT calculations applied to determine ArO-H bond dissociation enthalpies and reaction mechanism

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DOIResolve DOI: http://doi.org/10.1021/jo8016555
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TypeArticle
Journal titleJournal of Organic Chemistry
ISSN0022-3263
Volume73
Issue23
Pages92709282; # of pages: 13
SubjectActivation energy; Density functional theory; Deuterium; Hydrocarbons; O rings; Potential energy; Probability density function; Rate constants; Reaction kinetics; Sulfur compounds; Apolar solvents; Arrhenius; Atom abstractions; Complete basis sets; Correlated wave functions; Coupled cluster with single and double excitations; Cyclohexadiene; Deuterium kinetic isotope effects; DFT calculations; Electronic effects; Exponential factors; H-bonds; Kinetic measurements; Minimum energy structures; Phenoxyl radicals; Phenyl rings; Reaction coordinates; Reaction mechanisms; Semiquinone; Stacking interactions; Steric effects; Transition states; Unsaturated hydrocarbons; 1,1 diphenyl 2 picrylhydrazyl; 1,4 cyclohexadiene; alkene; deuterium; isotope; mequinol; phenol derivative; solvent; phenoxy radical; density functional theory; molecular dynamics; reaction analysis; conformation; solubility; thermodynamics; Models, Chemical; Models, Theoretical; Molecular Conformation; Nitrogen; Phenols
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LanguageEnglish
AffiliationNational Research Council Canada; National Institute for Nanotechnology; NRC Steacie Institute for Molecular Sciences
Peer reviewedYes
NPARC number21276705
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Record identifier04d040c1-cc87-44d6-8f60-1d8717eaa3d7
Record created2015-10-13
Record modified2016-05-09
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