Stability of alkyl carbocations
Thomas Hansen, Pascal Vermeeren, F. Matthias Bickelhaupt, Trevor A. Hamlin
Abstract
The traditional and widespread rationale behind the stability trend of alkyl-substituted carbocations is incomplete. Through state-of-the-art quantum chemical analyses, we quantitatively established a generally overlooked driving force behind the stability of carbocations, namely, that the parent substrates are substantially destabilized by the introduction of substituents, often playing a dominant role in solution. This stems from the repulsion between the substituents and the C-X bond.
Topics & Concepts
CarbocationAlkylComputational chemistryChemistryStability (learning theory)Quantum chemicalChemical physicsPhotochemistryMoleculeOrganic chemistryComputer scienceMachine learningChemical Reaction MechanismsCyclopropane Reaction MechanismsOrganic and Inorganic Chemical Reactions