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Updated: Jan 10, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Correlating topological indices with physicochemical properties in 15 polycyclic aromatic hydrocarbons
Zeming Huang1,2,3, Jing Zhao4, Bangbang Jin2
1School of Software, Pingdingshan University, Pingdingshan, 467000, China.
None:
[Formula: see text], a major air pollutant, often carries toxic components such as polycyclic aromatic hydrocarbons (PAHs), which pose potential health risks. This study investigated the relationships between five physicochemical properties-boiling point, molecular mass, enthalpy of vaporization, molar volume, and surface tension-of 15 PAHs and seven molecular topological indices (including the Wiener, Hyper-Wiener, Distance-degree, and Gutman indices) using regression analysis. Results indicated that the selected topological indices were strongly correlated with the properties of PAHs, with correlation coefficients generally exceeding 0.7. In particular, quadratic regression models based on the Distance-degree and Gutman indices showed a very high correlation with enthalpy of vaporization ($R = 0.998$). This work provides quantitative insights into the structure-property relationships of PAHs and may support further theoretical developments in the risk assessment and source control of [Formula: see text]-bound PAHs.
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