Study of the pericyclic [2π + 4π] nature of a set of cheletropic reactions: analysis of the electronic reaction mechanism through bond reactivity descriptors and the electronic bonding structure.

contextCheletropic reactions are a class of pericyclic transformations with significant importance in synthetic organic chemistry. Traditionally explained through orbital symmetry considerations under the Woodward-Hoffmann rules, these reactions are often modeled using wavefunction-based methods. However, this study adopts an electron-density-centered approach, with the aim of providing a detailed description and explanation of the studied reactions using reactivity descriptors derived from Density Functional Theory. By analyzing electronic bonding structures, natural bond orbitals, and bond reactivity indices, we aim to offer a more detailed understanding of the stereoelectronic factors governing the [2π + 4π] nature of these processes. This framework enables the identification of subtle features such as charge delocalization and bond reorganization at the transition states, contributing to a refined theoretical model for pericyclic reactivity. The methodology may also support the rational design of new stereoselective reactions based on local electronic properties.

methodsAll quantum chemical calculations were performed using Gaussian 16. Geometries and vibrational frequencies were calculated at the B3LYP/6-31G(d,p) level to identify stationary points. IRC calculations with a stepsize of 0.1 amu