Structure and Bonding in π-Stacked Perylenes: The Impact of Charge on Pancake Bonding

J Am Chem Soc. 2024 Apr 17;146(15):10465-10477. doi: 10.1021/jacs.3c14065. Epub 2024 Apr 5.

Abstract

Perylene (PER) is a prototype of polycyclic aromatic hydrocarbons (PAHs), which play a pivotal role in various functional and electronic materials due to favorable molecule-to-molecule overlaps, which enhance electronic transport. This study provides guidelines regarding the impact of molecular charge on pancake bonding, a form of strong π-stacking interaction. Pancake bonding significantly boosts interaction energies within the monopositive dimer ([(C20H12)2]•+ or PER2+), crucial for stabilizing aggregation and crystal formation. We discovered energetically feasible sliding and rotation pathways within the [(C20H12)2]•+ dimer, connecting different configurations found in the Cambridge Structural Database (CSD). The dimer's charge profoundly influences the pancake bond order (PBO) and the strength and structural preferences of pancake bonding. The most stable configuration is found in the monocationic state (PER2+), featuring a pancake bond order of 1/2 with one-electron multicenter bonding (1e/mc) with similar characteristics for charge -1. Increasing the total charge of the dimer to +2 or -2 leads to an unstable local minimum. Diverse distribution of pancake bonding types present in crystal structures is interpreted with modeling based on dimer computations with varying charges.