Excited-State (Anti)Aromaticity Explains Why Azulene Disobeys Kasha’s Rule

0575764 - ÚOCHB 2024 RIV US eng J - Journal Article
Dunlop, David - Ludvíková, Lucie - Banerjee, A. - Ottosson, H. - Slanina, Tomáš
Excited-State (Anti)Aromaticity Explains Why Azulene Disobeys Kasha’s Rule.
Journal of the American Chemical Society. Roč. 145, č. 39 (2023), s. 21569-21575. ISSN 0002-7863. E-ISSN 1520-5126
R&D Projects: GA MŠMT(CZ) LTC20076
Institutional support: RVO:61388963
Keywords : multicenter bond indexes * aromaticity * fluorescence
OECD category: Physical chemistry
Impact factor: 15, year: 2022
Method of publishing: Open access
https://doi.org/10.1021/jacs.3c07625

Fluorescence exclusively occurs from the lowest excited state of a given multiplicity according to Kasha’s rule. However, this rule is not obeyed by a handful of anti-Kasha fluorophores whose underlying mechanism is still understood merely on a phenomenological basis. This lack of understanding prevents the rational design and property-tuning of anti-Kasha fluorophores. Here, we propose a model explaining the photophysical properties of an archetypal anti-Kasha fluorophore, azulene, based on its ground- and excited-state (anti)aromaticity. We derived our model from a detailed analysis of the electronic structure of the ground singlet, first excited triplet, and quintet states and of the first and second excited singlet states using the perturbational molecular orbital theory and quantum-chemical aromaticity indices. Our model reveals that the anti-Kasha properties of azulene and its derivatives result from (i) the contrasting (anti)aromaticity of its first and second singlet excited states (S1 and S2, respectively) and (ii) an easily accessible antiaromaticity relief pathway of the S1 state. This explanation of the fundamental cause of anti-Kasha behavior may pave the way for new classes of anti-Kasha fluorophores and materials with long-lived, high-energy excited states.
Permanent Link: https://hdl.handle.net/11104/0345490