Guidelines for Tuning the Excited State Hückel-Baird Hybrid Aromatic Character of Pro-Aromatic Quinoidal Compounds

<p>The present study aims to provide a solid ground for the identification, characterization and controlled design of pro-aromatic quinoidal organic compounds holding conjugated rings with Hückel and/or Baird (singlet and triplet) excited state aromatic character, and expects to become a reference work for future studies on Baird-aromaticity. Concretely, we explore a wide range of compounds with a central conjugated ring of different sizes and symmetric exocyclic substitutions. We employ a combination of different computational tools and we also introduce a new energy-based approach for the quantification of the Baird-aromatic character. </p> <p> </p> The key findings of this study indicate that Baird aromaticity is achieved in pro-aromatic quinoidal compounds having small anionic rings or in electron deficient rings with the proper exocyclic substitution. Low-lying states of these systems show very strong hole/electron overlaps, implying that their aromaticity cannot be related to intramolecular charge transfer.