Abstract
We report the results of a computational investigation into fluoride binding by a series of pentavalent pnictogen Lewis acids: pnictogen pentahalides (PnX5), tetraphenyl pnictogeniums (PnPh4+), and triphenyl pnictogen tetrachlorocatecholates (PnPh3Cat). Activation strain and energy decomposition analyses of the Lewis adducts clearly delineate the electrostatic and orbital contributions to these acid-base interactions, but they also highlight the importance of Pauli repulsion and molecular flexibility in determining relative Lewis acidity among the pnictogens.
Supplementary materials
Title
Supporting Information
Description
This document contains details about our calculations, atomic coordinate tables, and energies.
Actions