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Updated: Jun 5, 2025

Computation of Atmospheric Concentrations of Molecular Clusters from ab initio Thermochemistry
Published on: April 8, 2020
Predicting enthalpy of formation of benzenoid hydrocarbons and ordering molecular trees using general multiplicative
Sadia Noureen1, Akbar Ali2, Akhlaq A Bhatti3
1Faculty of Science, University of Gujrat, Gujrat, Pakistan.
Abstract:
Many existing studies show that there exists a strong relationship between structures and characteristics of molecules. Topological indices are often used in modeling the properties of chemical compounds and biological activities in theoretical chemistry. Topological indices are numerical values associated with structures of molecules in such a way that they remain constant under graph isomorphism. Multiplicative Zagreb indices are among the famous topological indices that have been explored by numerous researchers in the last few years. The first objective of the present paper is to examine the importance of general multiplicative Zagreb indices for forecasting the enthalpy of formation of hydrocarbons using a data set of 25 benzenoid hydrocarbons. The second objective of this paper is to study molecular trees with a given order and with a given number of branching vertices or segments using general multiplicative (first and second) Zagreb indices. Sharp lower/upper bounds on these Zagreb indices for the aforementioned molecular trees are obtained and the graphs attaining these bounds are determined. Bounds on the classical multiplicative Zagreb and Narumi-Katayama indices are corollaries of the obtained results.
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