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تسجيل مستخدم جديدOrdering chemical graphs by Sombor indices and its applications
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Topological indices are a class of numerical invariants that predict certain physical and chemical properties of molecules. Recently, two novel topological indices, named as Sombor index and reduced Sombor index, were introduced by Gutman, defined as $$SO(G)=sum_{uvin E(G)}sqrt{d_{G}^{2}(u)+d_{G}^{2}(v)},$$ $$SO_{red}(G)=sum_{uvin E(G)}sqrt{(d_{G}(u)-1)^{2}+(d_{G}(v)-1)^{2}},$$ where $d_{G}(u)$ denotes the degree of vertex $u$ in $G$. In this paper, our aim is to order the chemical trees, chemical unicyclic graphs, chemical bicyclic graphs and chemical tricyclic graphs with respect to Sombor index and reduced Sombor index. We determine the first fourteen minimum chemical trees, the first four minimum chemical unicyclic graphs, the first three minimum chemical bicyclic graphs, the first seven minimum chemical tricyclic graphs. At last, we consider the applications of reduced Sombor index to octane isomers.
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Hexagonal chains are a special class of catacondensed benzenoid system and phenylene chains are a class of polycyclic aromatic compounds. Recently, A family of Sombor indices was introduced by Gutman in the chemical graph theory. It had been examined
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Sombor index is a novel topological index introduced by Gutman, defined as $SO(G)=sumlimits_{uvin E(G)}sqrt{d_{u}^{2}+d_{v}^{2}}$, where $d_{u}$ denotes the degree of vertex $u$. Recently, Chen et al. [H. Chen, W. Li, J. Wang, Extremal values on the
Sombor index of trees, MATCH Commun. Math. Comput. Chem. 87 (2022), in press] considered the Sombor indices of trees with given diameter. For the continue, we determine the maximum Sombor indices for unicyclic graphs with given diameter.
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