Extension and Quantification of the Fries Rule and Its Connection to Aromaticity: Large-Scale Validation by...

The Fries rule is a simple, intuitive tool to predict the most dominant Kekulé structures of polycyclic aromatic hydrocarbons (PAHs), which is valuable for understanding the structure, stability, reactivity, and aromaticity of these conjugated compounds. However, it still remains an empirical hypothesis, with limited qualitative applications. Herein, we verify, generalize, and quantify the Fries rule based on the recently developed resonance analysis of the DFT wave functions of over 1500 PAH and fullerene molecules with over a billion Kekulé structures. The extended rules, counting the numbers of electrons within all rings (not just sextets), are able to rank the relative importance of all Kekulé structures for all considered systems. The statistically meaningful quantification also opens a way to evaluate ring aromaticity based on the resonance theory, which generally agrees well with conventional aromaticity descriptors. Furthermore, we propose a purely graph-based aromaticity indicator nicely applicable to PAHs and fullerenes, with no need of any quantum chemistry calculations, so that it can make valuable predictions for molecular properties that are related to local aromaticity.