Litcius/Paper detail

Stability of alkyl carbocations

Thomas Hansen, Pascal Vermeeren, F. Matthias Bickelhaupt, Trevor A. Hamlin

2022Chemical Communications16 citationsDOIOpen Access PDF

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