Polarity of the Transition State Controls the Reactivity of Related Charged Phenyl Radicals Toward Atom and Group Donors
- 21 March 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 66 (8) , 2726-2733
- https://doi.org/10.1021/jo001634r
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Comparison of the Addition of CH3.bul., CH2OH.bul., and CH2CN.bul. Radicals to Substituted Alkenes: A Theoretical Study of the Reaction MechanismJournal of the American Chemical Society, 1994
- Adiabatic ionization energy of CH3SSCH3The Journal of Chemical Physics, 1993
- Sustained off-resonance irradiation for collision-activated dissociation involving Fourier transform mass spectrometry. Collision-activated dissociation technique that emulates infrared multiphoton dissociationAnalytica Chimica Acta, 1991
- Reactions of dihalobenzene radical cations with ammonia in the gas phase. Reactivity pattern for nucleophilic aromatic substitutionJournal of the American Chemical Society, 1991
- Iminoyl free radicals. Electron spin resonance identification of a new class of .sigma. radicalsJournal of the American Chemical Society, 1973
- Halogen abstraction studies. II. Free-radical abstraction of iodine from bridgehead iodidesJournal of the American Chemical Society, 1971
- Halogen abstraction reactions. I. Free-radical abstraction of iodine from substituted iodobenzenesJournal of the American Chemical Society, 1969
- Radical Abstraction of Iodine from Aryl Iodides1Journal of the American Chemical Society, 1966
- Rates of the Reactions of Substituted Phenyl Radicals with Hydrogen Donors1,2Journal of the American Chemical Society, 1966
- Walden Inversion by Radicals. The Reaction of Phenyl Radicals with DisulfidesJournal of the American Chemical Society, 1964