Density functional theory study of hydrogen atom abstraction from a series of para-substituted phenols: why is the Hammett σ(p)+ constant able to represent radical reaction rates?

scientific article published on 02 May 2011

Density functional theory study of hydrogen atom abstraction from a series of para-substituted phenols: why is the Hammett σ(p)+ constant able to represent radical reaction rates? is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1021/JO200450P
P698PubMed publication ID21500806

P2093author name stringMasataka Harada
Hiroshi Chuman
Seiji Hitaoka
Tatsusada Yoshida
Koji Hirozumi
P433issue11
P921main subjectdensity functional theoryQ1048589
P304page(s)4564-4570
P577publication date2011-05-02
P1433published inJournal of Organic ChemistryQ898967
P1476titleDensity functional theory study of hydrogen atom abstraction from a series of para-substituted phenols: why is the Hammett σ(p)+ constant able to represent radical reaction rates?
P478volume76

Reverse relations

cites work (P2860)
Q86590241A single theoretical descriptor for the bond-dissociation energy of substituted phenols
Q59711702Assessment of theoretical methods for the study of hydrogen abstraction kinetics of global warming gas species during their degradation and byproduct formation (IUPAC Technical Report)
Q90609955Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex

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