Submitted:
20 January 2025
Posted:
21 January 2025
You are already at the latest version
Abstract
Keywords:
MSC: 05C07; 05C09; 05C92
1. Introduction
2. The Euler Sombor and Gourava Sombor Coindices
2.1. Bounds for Euler Sombor Coindex and Gourava Sombor Coindex Depending on Some Other Topological Coindices
2.2. Bounds on the Euler Sombor Coindex and Gourava Sombor Coindex of Graph Operations
3. The Euler Sombor and Gourava Sombor Coindices of SOME chemical Graphs
4. The Use of Selected Sombor Topological Indices and Coindices in QSPR Studies
| Compound | HBAC | HAC | COMP | ST |
| 1,4-butanedithiol | 2 | 6 | 17.5 | 31.1 |
| 2-butanone | 1 | 5 | 38.5 | 22.9 |
| 1,3-butanediol | 2 | 6 | 28.7 | 34.9 |
| butane dinitrile | 2 | 6 | 92 | 40.7 |
| butanediamide | 2 | 8 | 96.6 | 53 |
| butane-1-sulfoamide | 3 | 8 | 133 | 41.9 |
| 1-butanethiol | 1 | 5 | 13.1 | 24.8 |
| 1,4-diaminobuane | 2 | 6 | 17.5 | 35.8 |
| butane-1,4-disulfonic acid | 6 | 12 | 266 | 77.9 |
| butyraldehyde | 1 | 5 | 24.8 | 23.1 |
| 2,3-butanedione | 2 | 6 | 71.5 | 27.3 |
| 1-butanesufonylchloride | 2 | 8 | 133 | 36.4 |
| Compound | ||||
| 1,4-butanedithiol | 24.18 | 15.68 | 27.99 | 40.83 |
| 2-butanone | 30 | 17.81 | 17.71 | 25.11 |
| 1,3-butanediol | 27.07 | 17.67 | 26.38 | 37.54 |
| butane dinitrile | 53.44 | 26.21 | 52.30 | 96.91 |
| butanediamide | 58.46 | 33.79 | 77.47 | 130.05 |
| butane-1-sulfoamide | 85.92 | 49.98 | 91.83 | 149.39 |
| 1-butanethiol | 18.52 | 17.51 | 26.36 | 22.31 |
| 1,4-diaminobuane | 24.18 | 20.97 | 27.99 | 40.83 |
| butane-1,4-disulfonic acid | 121.94 | 66.77 | 231.47 | 390.13 |
| butyraldehyde | 24.88 | 14.82 | 20.18 | 31.33 |
| 2,3-butanedione | 50.69 | 30.13 | 35.52 | 55.12 |
| 1-butanesufonylchloride | 67.40 | 37.76 | 74.23 | 118 |
- Non-linear Regression Model:





5. Results and Discussion
Author Contributions
Funding
Conflicts of Interest
References
- Bondy, J.A.; Murty, U.S.R. Graph Theory with Applications, 1 Eds., New York: Macmillan Press, (1976).
- Kulli, V.R. College Graph Theory, Gulbarga: Vishwa International Publications, (2012).
- Gutman, I. Geometric approach to degree-based topological indices: Sombor indices. MATCH Commun. Math. Comput. Chem. 2021, 86, 11–16. [Google Scholar]
- Kulli, V.R. Delta Banhatti-Sombor indices of certain networks. Int. J. Math. Comput. Res. 2023, 11, 3875–3881. [Google Scholar] [CrossRef]
- Kulli, V.R. Modified domination Sombor index and its exponential of a graph. Int. J. Math. Comput. Res. 2023, 11, 3639–3644. [Google Scholar] [CrossRef]
- Khalifeh, M.H.; Yousefi-Azari, H.; Ashrafi, A.R. The first and second Zagreb indices of some graph operations. Discrete Appl. Math. 2009, 157, 804–811. [Google Scholar] [CrossRef]
- Furtula, B.; Gutman, I. A forgotten topological index. J. Math. Chem. 2015, 53, 1184–1190. [Google Scholar] [CrossRef]
- Gök, G.K. On the Forgetten Topological Index and Co Index. EJOSAT 2019, 15, 308–314. [Google Scholar] [CrossRef]
- Ashrafi, A.R.; Doslic, T.; Hamzeh, A. The Zagreb coindices of graph operations. Discrete Appl. Math. 2010, 158, 1571–1578. [Google Scholar] [CrossRef]
- Gök, G.K. On The Reformulated Zagreb Coindex. JNT 2019, 28, 28–32. [Google Scholar]
- Das, K.C.; Cevik, A.S.; Shang, Y. On sombor index. Symmetry 2021, 13, 140. [Google Scholar] [CrossRef]
- Du, Z.; You, L.; Liu, H.; Huang, Y. The Sombor index and coindex of two-trees. AIMS Mathematics 2023, 8, 18982–18994. [Google Scholar] [CrossRef]
- Saidi, N.H.A.M.; Husin, M.N.; Ismail, N.B. On the Zagreb Indices of the Line Graphs of Polyphenylene Dendrimers. Journal of Discrete Mathematical Sciences and Cryptography 2020, 23, 1239–1252. [Google Scholar] [CrossRef]
- Redzepovic, I. Chemical Applicability of Sombor Indices. Journal of the Serbian Chemical Society 2021, 86, 445–457. [Google Scholar] [CrossRef]
- Ghalavand, A.; Ashrafi, A.R. On Forgotten Coindex of Chemical Graphs. MATCH Communications in Mathematical and in Computer Chemistry 2020, 83, 221–232. [Google Scholar]
- Du, Z.; You, L.; Liu, H. The Sombor Index and Coindex of Chemical Graphs. Polycyclic Aromatic Compounds 2024, 44, 2942–2965. [Google Scholar] [CrossRef]
- Wazzan, S.; Ahmed, H. Symmetry-adapted domination indices: The enhanced domination sigma index and its applications in QSPR studies of octane and its isomers. Symmetry 2023, 15, 1202. [Google Scholar] [CrossRef]
- Wazzan, S.; Ahmed, H. Advancing computational insights: Domination topological indices of polysaccharides des using special polynomials and QSPR analysis. Contemp. Math. 2024, 5, 26–49. [Google Scholar] [CrossRef]
- Gutman, I.; Furtula, B.; Oz, M.S. Geometric approach to vertex-degree-based topological indices - Elliptic Sombor index, theory and application. Int. J. Quantum Chem 2024, 124, e27346. [Google Scholar] [CrossRef]
- Tang, Z.; Li, Y.; Deng, H. The Euler Sombor index of a graph, Int. J. Quantum Chem. 2024, 124, e27387. [Google Scholar] [CrossRef]
- Kulli, V.R. The Gourava Indices and Coindices of Graphs. Annals of Pure and Applied Mathematics 2014, 1, 33–8. [Google Scholar] [CrossRef]
- Doslic, T. Vertex-weighted wiener polynomials for composite graphs. ARS Math. Contemp. 2008, 1, 66–81. [Google Scholar] [CrossRef]
- Pattabiraman, K.; Vijayaragavan, M. Hyper Zagreb indices and its coindices of graphs. Bull. Inter. Math. Virtual Inst. 2017, 7, 31–41. [Google Scholar]
- De, N.; Nayeem, S.; Pal, A. The F-coindex of some graph operations. SpringerPlus. [CrossRef]
- Alameri, A. New binary operations on graphs. JST 2016, 21, 97–116. [Google Scholar] [CrossRef]
- Dragomir, S.S. A survey on Cauchy-Bunyakovsky-Schwarz type discrete inequalities. J. Inequal. Pure Appl. Math. 2003, 4, 63–202. [Google Scholar]
- Ramirez, R.E.H.; Lijanova, I.V.; Likhanova, N.V.; Xometl, O.O. PAMAM Dendrimers with Porphyrin Core: Synthesis and Metal-Chelating Behavior. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2016, 84, 49–60. [Google Scholar] [CrossRef]
- Manzoor, S.; Siddiqui, M.K.; Ahmad, S. On Computation of Entropy Measures for Phthalocyanines and Porphyrins Dendrimers. International Journal of Quantum Chemistry 2022, 122, e26854. [Google Scholar] [CrossRef]
- PubChem Available from: https://pubchem.ncbi.nlm.nih.
- Shashidhara, A.A.; Ahmed, H.; Nandappa, S.; Cancan, M. Domination version: Sombor index of graphs and its significance in predicting physicochemical properties of butane derivatives. Eurasian Chem. Commun. 2023, 5, 91–102. [Google Scholar] [CrossRef]
| Introduced by | Index Name | Notation | Formula |
| [19,20] | Euler Sombor index | ||
| [21] | Gourava Sombor index | ||
| [22]Doslic, 2008 | First Zagreb coindex | ||
| [22]Doslic, 2008 | Second Zagreb coindex | ||
| [23]Pattabiraman and Vijayaravan, 2017 | First Hyper-Zagreb coindex | ||
| [23]Pattabiraman and Vijayaravan, 2017 | Second Hyper-Zagreb coindex | ||
| [24]De,N.,Abu Nayeem, Sk. Md. and Pal, A. 2016 | Forgetten coindex |
| Compound | ||||
| 1,4-butanedithiol | 1.335459 | 1.244092 | 1.482178 | 1.508217 |
| 2-butanone | 1.541408 | 1.386579 | 1.139355 | 1.176683 |
| 1,3-butanediol | 1.439583 | 1.377295 | 1.432565 | 1.444889 |
| butane dinitrile | 2.262888 | 1.926617 | 2.122906 | 2.344972 |
| butanediamide | 2.402111 | 2.391729 | 2.660681 | 2.724976 |
| butane-1-sulfoamide | 3.103163 | 3.337642 | 2.933831 | 2.924869 |
| 1-butanethiol | 1.118441 | 1.366671 | 1.431941 | 1.10775 |
| 1,4-diaminobuane | 1.335459 | 1.593424 | 1.482178 | 1.508217 |
| butane-1,4-disulfonic acid | 3.91669 | 4.270912 | 4.990947 | 4.774956 |
| butyraldehyde | 1.361045 | 1.185762 | 1.228135 | 1.317453 |
| 2,3-butanedione | 2.184768 | 2.169334 | 1.69967 | 1.757965 |
| 1-butanesufonylchloride | 2.640528 | 2.628947 | 2.59615 | 2.59299 |
| Compound | ||||
| 1,4-butanedithiol | 5.32036 | 5.112493 | 5.646162 | 5.721763 |
| 2-butanone | 5.776376 | 5.439739 | 4.854167 | 4.978076 |
| 1,3-butanediol | 5.554397 | 5.418869 | 5.536788 | 5.585738 |
| butane dinitrile | 7.198875 | 6.566213 | 6.940683 | 7.328943 |
| butanediamide | 7.449591 | 7.431088 | 7.902143 | 7.973089 |
| butane-1-sulfoamide | 8.627785 | 8.992146 | 8.358541 | 8.296045 |
| 1-butanethiol | 4.805966 | 5.394912 | 5.535402 | 4.812333 |
| 1,4-diaminobuane | 5.32036 | 5.890203 | 5.646162 | 5.721763 |
| butane-1,4-disulfonic acid | 9.859995 | 10.3546 | 11.34251 | 10.92113 |
| butyraldehyde | 5.378571 | 4.973932 | 5.068015 | 5.303816 |
| 2,3-butanedione | 7.055309 | 7.027489 | 6.108283 | 6.235286 |
| 1-butanesufonylchloride | 7.864972 | 7.84426 | 7.79145 | 7.754118 |
| Compound | ||||
| 1,4-butanedithiol | 5.32036 | 5.112493 | 5.646162 | 5.721763 |
| 2-butanone | 5.776376 | 5.439739 | 4.854167 | 4.978076 |
| 1,3-butanediol | 5.554397 | 5.418869 | 5.536788 | 5.585738 |
| butane dinitrile | 7.198875 | 6.566213 | 6.940683 | 7.328943 |
| butanediamide | 7.449591 | 7.431088 | 7.902143 | 7.973089 |
| butane-1-sulfoamide | 8.627785 | 8.992146 | 8.358541 | 8.296045 |
| 1-butanethiol | 4.805966 | 5.394912 | 5.535402 | 4.812333 |
| 1,4-diaminobuane | 5.32036 | 5.890203 | 5.646162 | 5.721763 |
| butane-1,4-disulfonic acid | 9.859995 | 10.3546 | 11.34251 | 10.92113 |
| butyraldehyde | 5.378571 | 4.973932 | 5.068015 | 5.303816 |
| 2,3-butanedione | 7.055309 | 7.027489 | 6.108283 | 6.235286 |
| 1-butanesufonylchloride | 7.864972 | 7.84426 | 7.79145 | 7.754118 |
| Compound | ||||
| 1,4-butanedithiol | 5.32036 | 5.112493 | 5.646162 | 5.721763 |
| 2-butanone | 5.776376 | 5.439739 | 4.854167 | 4.978076 |
| 1,3-butanediol | 5.554397 | 5.418869 | 5.536788 | 5.585738 |
| butane dinitrile | 7.198875 | 6.566213 | 6.940683 | 7.328943 |
| butanediamide | 7.449591 | 7.431088 | 7.902143 | 7.973089 |
| butane-1-sulfoamide | 8.627785 | 8.992146 | 8.358541 | 8.296045 |
| 1-butanethiol | 4.805966 | 5.394912 | 5.535402 | 4.812333 |
| 1,4-diaminobuane | 5.32036 | 5.890203 | 5.646162 | 5.721763 |
| butane-1,4-disulfonic acid | 9.859995 | 10.3546 | 11.34251 | 10.92113 |
| butyraldehyde | 5.378571 | 4.973932 | 5.068015 | 5.303816 |
| 2,3-butanedione | 7.055309 | 7.027489 | 6.108283 | 6.235286 |
| 1-butanesufonylchloride | 7.864972 | 7.84426 | 7.79145 | 7.754118 |
| Properties | ||||
| HBAC | 0.8419 | 0.8783 | 0.9277 | 0.9174 |
| HAC | 0.8897 | 0.9221 | 0.9748 | 0.9610 |
| COMP | 0.9855 | 0.9630 | 0.9506 | 0.9619 |
| ST | 0.8137 | 0.8306 | 0.9344 | 0.9332 |
| Indices | HBAC | HAC | COMP | ST |
|---|---|---|---|---|
| GSO | 0.7464 | 0.7687 | 0.9724 | 0.9840 |
| EU | 0.7840 | 0.8336 | 0.8419 | 0.9751 |
| 0.8322 | 0.9287 | 0.7615 | 0.9867 | |
| 0.8455 | 0.9091 | 0.8366 | 0.9879 |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).