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Adjustment of the Proton‐Accepting Ability of Π‐Bonds and Lone Pairs

Akhtam AmonovDepartment of Optics and Spectroscopy Engineering Physics Institute Samarkand State University University blv. 15 140104 Samarkand UzbekistanSteve ScheinerDepartment of Chemistry and Biochemistry Utah State University Logan Utah 84322‐0300 USA
ChemPhysChemjournal2025en
ABI

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A hydroxyl group is placed on a series of systems containing CC double bonds, and quantum chemical calculations consider the preferred target of an incoming1 HCl molecule to form an H‐bond. The O lone pairs are favored over the π‐system in most instances but can be reversed by the presence of electron‐donating substituents. This reversal occurs when NH 2 groups are added to a simple alkene or if NMe 2 substituents are placed on a conjugated butadiene derivative. There are a variety of means of favoring the aromatic ring as a proton‐accepting site over the phenol O. Dispersion is the primary factor in determining the preferred electron‐donor site in the aromatic systems. The particular site and orientation of attachment of HCl to the π system is controlled by a combination of electrostatic potential and HOMO disposition.

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