Publication | Closed Access
Reactions of Carbocations with π Nucleophiles: Polar Mechanism and No Outer Sphere Electron Transfer
46
Citations
15
References
1995
Year
EngineeringNuclear PhysicsSingle Electron TransferProton-coupled Electron TransferOrganic ChemistryChemistryReaction Intermediateπ Nucleophilesπ-Electron SystemsBiochemistryPhysicsRadical (Chemistry)Polar MechanismAtomic PhysicsCatalysisQuantum ChemistryBiomolecular EngineeringNatural SciencesHalogenationChemical KineticsRate Constants
Rate constants at least eight orders of magnitude greater than those calculated for the single electron transfer (SET) process are observed for the addition of R+ to π-electron systems. Thus it is clear that in these reactions radical intermediates are generally not found, but that charge transfer is associated with the formation of the new CC σ bond.
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