On Degree Based Topological Aspects of Some Dendrimers

References

• E. Buhleier, W. Wehner, and F. Vögtle, “Cascade and Nonskid-Chain-like Synthesis of Molecular Cavity Topologies,” Synthesis 1978, no. 02 (1978): 155–8. doi:10.1055/s-1978-24702.
   Google Scholar
• M. N. Husin, R. Hasni, and N. E. Arif, “Zagreb Polynomials of Some Nanostar Dendrimers,” Journal of Computational and Theoretical Nanoscience 12, no. 11 (2015): 4297–300. doi:10.1166/jctn.2015.4354.
   Google Scholar
• N. H. A. M. Saidi, M. N. Husin, and N. B. Ismail, “On the Topological Indices of the Lines Graphs of Polyphenylene Dendrimer,” AIP Conference Proceedings, 2021. 23–65.
   Google Scholar
• H. Abdo, D. Dimitrov, and I. Gutman, “On External Trees with Respect to the F-Index,” Kuwait Journal of Science 44, no. 3 (2017): 1–8.
   Web of Science ®Google Scholar
• N. H. A. M. Saidi, M. N. Husin, and N. B. Ismail, “On the Zagreb Indices of the Line Graphs of Polyphenylene Dendrimers,” Journal of Discrete Mathematical Sciences and Cryptography 23, no. 6 (2020): 1239–52. doi:10.1080/09720529.2020.1822041.
   Web of Science ®Google Scholar
• M. N. Husin, R. Hasni, and M. Imran, “More Results on Computational of Topological Indices of Certain Networks,” International Journal of Networking and Virtual Organisations 17, no. 1 (2017): 46–63. doi:10.1504/IJNVO.2017.083543.
   Google Scholar
• A. R. Ashrafi, and M. Mirzargar, “PI, Szeged and Edge Szeged of an Infi Family of Nanostar Dendrimers,” Indian Journal of Chemistry 47A (2008): 538–41.
   Google Scholar
• M. V. Diudea, A. E. Vizitiu, and M. Mirzagar, “Sadhana Polynomial in Nano-Dendrimers,” Carpathian Journal of Mathematics 26 (2010): 59–66.
   Web of Science ®Google Scholar
• S. Biswas, and V. Torchilin, “Dendrimers for siRNA Delivery,” Pharmaceuticals (Basel, Switzerland) 6, no. 2 (2013): 161–83. doi:10.3390/ph6020161.
   PubMedGoogle Scholar
• M. Kalomiraki, K. Thermos, and N. Chaniotakis, “Dendrimers as Tunable Vectors of Drug Delivery Systems and Biomedical and Ocular Applications,” International Journal of Nanomedicine 11 (2016): 1–12. doi:10.2147/IJN.S93069.
   PubMed Web of Science ®Google Scholar
• P. Kesharwani, K. Jain, and N. K. Jain, “Dendrimer as Nanocarrier for Drug Delivery,” Progress in Polymer Science 39, no. 2 (2014): 268–307. doi:10.1016/j.progpolymsci.2013.07.005.
   Web of Science ®Google Scholar
• M. Liu, and J. M. Fréchet, “Designing Dendrimers for Drug Delivery,” Pharmaceutical Science & Technology Today 2, no. 10 (1999): 393–401. doi:10.1016/S1461-5347(99)00203-5.
   PubMedGoogle Scholar
• S. Svenson, and D. A. Tomalia, “Dendrimers in Biomedical Applications Reflections on the Field,” Advanced Drug Delivery Reviews 64 (2012): 102–15. doi:10.1016/j.addr.2012.09.030.
   Web of Science ®Google Scholar
• D. Vukičević, and M. Gašperov, “Bond Additive Modelling 1. Adriatic Indices,” Croatica Chemica Acta 83 (2010): 261–73.
   Web of Science ®Google Scholar
• S. Hafeez, and R. Farooq, School of Natural Sciences, National University of Sciences and Technology, H-12 Islamabad, Pakistan“On Generalized Inverse Sum Indeg Index and Energy of Graphs,” AIMS Mathematics 5, no. 3 (2020): 2388–411. doi:10.3934/math.2020158.
   Web of Science ®Google Scholar
• I. Gutman, and N. Trinajstić, “Graph Theory and Molecular Orbitals. Total π-Electron Energy of Alternant Hydrocarbons,” Chemical Physics Letters 17, no. 4 (1972): 535–8. doi:10.1016/0009-2614(72)85099-1.
   Web of Science ®Google Scholar
• M. Ghorbani, and M. A. Hosseinzadeh, “A New Version of Zagreb Indices,” Filomat 26, no. 1 (2012): 93–100. doi:10.2298/FIL1201093G.
   Web of Science ®Google Scholar
• B. Zhou, and N. Trinajstić, “On General Sum-Connectivity Index,” Journal of Mathematical Chemistry 47, no. 1 (2010): 210–8. doi:10.1007/s10910-009-9542-4.
   Web of Science ®Google Scholar
• B. Bollobás, and P. Erdös, “Graphs of Extremal Weights,” Ars. Combination 50 (1998): 225–33.
   Web of Science ®Google Scholar
• D. Vukičević, and B. Furtula, “Topological Index Based on the Ratios of Geometrical and Arithmetical Means of End-Vertex Degrees of Edges,” Journal of Mathematical Chemistry 46 (2000): 1369–76.
   Google Scholar
• M. Ghorbani, and A. Khaki, “A Note on the Fourth Version of Geometric-Arithmetic Index,” Optoelectronics and Advanced Materials, Rapid Communications. 4 (2010): 2212–5.
   Web of Science ®Google Scholar
• M. Liu, “A Simple Approach to Order the First Zagreb Indices of Connected Graphs,” MATCH Communications in Mathematical and in Computer Chemistry 63 (2010): 425–32.
   Web of Science ®Google Scholar
• S. Ediz, M. R. Farahani, and M. Imran, “On Novel Harmonic Indices of Certain Nanotubes,” International Journal of Advanced Biotechnology and Research 8, no. 4 (2017): 87–92.
   Google Scholar
• J. J. Cid, J. H. Yum, S. R. Jang, M. K. Nazeeruddin, E. Martínez-Ferrero, E. Palomares, J. Ko, M. Grätzel, and T. Torres, “Molecular Cosensitization for Efficient Panchromatic Dye-Sensitized Solar Cells,” Angewandte Chemie (International ed. in English) 46, no. 44 (2007): 8358–62. doi:10.1002/anie.200703106.
   PubMed Web of Science ®Google Scholar
• I. López-Duarte, M. Wang, R. Humphry-Baker, M. Ince, M. V. Martínez-Díaz, M. K. Nazeeruddin, T. Torres, and M. Grätzel, “Molecular Engineering of Zinc Phthalocyanines with Phosphinic Acid Anchoring Groups,” Angewandte Chemie (International ed. in English) 51, no. 8 (2012): 1895–8. doi:10.1002/anie.201105950.
   PubMed Web of Science ®Google Scholar
• F. Setaro, R. Ruiz-González, S. Nonell, U. Hahn, and T. Torres, “Synthesis, Photophysical Studies and 1O2 Generation of Ruthenium Phthalocyanine Dendrimers,” Journal of Porphyrins and Phthalocyanines 20 (2016): 378–87.
   Web of Science ®Google Scholar
• H. Chang, H. Wang, N. Shao, M. Wang, X. Wang, and Y. Cheng, “Surface-Engineered Dendrimers with a Diaminododecane Core Achieve Efficient Gene Transfection and Low Cytotoxicity,” Bioconjugate Chemistry 25, no. 2 (2014): 342–50. doi:10.1021/bc400496u.
   PubMed Web of Science ®Google Scholar
• R. Esfand, and D. A. Tomalia, “Poly(Amidoamine) (PAMAM) Dendrimers: From Biomimicry to Drug Delivery and Biomedical Applications,” Drug Discovery Today 6, no. 8 (2001): 427–36. doi:10.1016/S1359-6446(01)01757-3.
   PubMed Web of Science ®Google Scholar
• S. Lalwani, A. Chouai, L. M. Perez, V. Santiago, S. Shaunak, and E. E. Simanek, “Mimicking PAMAM Dendrimers with Amphoteric, Hybrid Triazine Dendrimers: A Comparison of Dispersity and Stability,” Macromolecules 42, no. 17 (2009): 6723–32. doi:10.1021/ma9011818.
   PubMed Web of Science ®Google Scholar
• D. M. Watkins, Y. Sayed-Sweet, J. W. Klimash, N. J. Turro, and D. A. Tomalia, “Dendrimers with Hydrophobic Cores and the Formation of Supramolecular Dendrimer-Surfactant Assemblies,” Langmuir 13, no. 12 (1997): 3136–41. doi:10.1021/la9620263.
   Web of Science ®Google Scholar
• R. E. H. Ramirez, I. V. Lijanova, N. V. Likhanova, and O. O. Xometl, “PAMAM Dendrimers with Porphyrin Core: Synthesis and Metal-Chelating Behavior,” Journal of Inclusion Phenomena and Macrocyclic Chemistry 84, no. 1–2 (2016): 49–60. doi:10.1007/s10847-015-0582-z.
   Web of Science ®Google Scholar