Polycyclic Hydrocarbons from [4n]Annulenes: Correlation versus Hybridization Forces in the Formation of Diradicaloids

The conceptual connections between [4n] Huckel antiaromaticity, disjoint orbitals, correlation energy, pro-aromaticity and diradical character for a variety of extended pi-conjugated systems, including some salient recent examples of nanographenes and polycyclic aromatic radicals, are provided based on their [4n]annulene peripheries. The realization of such structure-property relationships has led to a beneficial pedagogic exercise establishing design guidelines for diradicaloids. The antiaromatic fingerprint of the [4n]annulene peripheries upon orbital interactions due to internal covalent connectors gives insights into the diradicaloid property of a diversity of pi-conjugated molecules that have fascinated chemists recently.

Automated summary

This article provides conceptual connections between [4n] Huckel antiaromaticity, disjoint orbitals, correlation energy, pro-aromaticity and diradical character for a variety of extended pi-conjugated systems, including nanographenes and polycyclic aromatic radicals. Understanding these structure-property relationships is beneficial for establishing design guidelines for diradicaloids.