Relation between second and third geometric–arithmetic indices of trees
By Boris Furtula, Ivan Gutman. 2011
50 citations recorded by the source corpus.
Subfields: Computational Theory and Mathematics, Geometry and Topology, Organic Chemistry
View Paper: https://www.semanticscholar.org/paper/00ca9fd77af838d5a66965b2c479ca0d2123c8b6
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Computational Theory and Mathematics
- Danuta Leszczynska
- Andrey A. Toropov
- Emilio Benfenati
- Alla P. Toropova
- Giuseppina C. Gini
- Jerzy Leszczynski
In Organic Chemistry
- Danuta Leszczynska
- Andrey A. Toropov
- Emilio Benfenati
- Alla P. Toropova
- Giuseppina C. Gini
- Jerzy Leszczynski
Citations in the corpus
- CORAL: QSPR model of water solubility based on local and global SMILES attributes. (2013, background): “Quantitative structure – property/activity relationships (QSPRs/QSARs) based on various molecular descriptors (Furtula and Gutman, 2011; Melagraki and Afantitis, 2011; Mullen et al., 2011; Ojha et al., 2011) are a possible tool to predict physicochemical properties (Huuskonen, 2000; Tetko et al.”
- Analytical expressions for topological properties of polycyclic benzenoid networks (2016, unknown): “Recently the Wiener indices for the following structures have been reported in the work of Quadras et al(50): (1) Circum-naphthalenes(n), (2) Circum-anthracenes(n), (3) Circum-tetracenes(n), (4) Circum-pentacenes(n), (5) Circum-hexacenes(n), (6) Circum-pyrenes(n), (7) Circum-trizenes(n), (8) Circum-”