78
Views
0
CrossRef citations to date
0
Altmetric
Research Article

Preparation of branched polystyrene via atom transfer radical polymerisation using diene with electron-rich double bond

ORCID Icon, , , , , , & show all
Pages 447-451 | Received 26 Aug 2020, Accepted 07 Sep 2020, Published online: 16 Sep 2020

References

  • VoitandA Lederer: BI. Hyperbranched and highly branched polymer architectures – synthetic strategies and major characterization aspects. Chem Rev. 2009;109:5924–5973.
  • Haidan G, Wenyan H, Dongliang Z, et al. Studies on the development of branching in ATRP of styrene and acrylonitrile in the presence of divinylbenzene. Polymer. 2008;49:4101–4108.
  • Ren Q, Gong F, Liu C, et al. Synthesis of branched polystyrene by ATRP exploiting divinylbenzene as branching comonomer. Eur Polym J. 2006;42:2573–2580.
  • Gong F, Tang H, Liu C, et al. Preparation of hyperbranched polymers through ATRP of in situ formed AB* monomer. J Appl Polym Sci. 2006;101:850–856.
  • Huang W, Sun P, Xue X, et al. Studies on the branching atom transfer radical polymerization using different divinyl monomers as the branching agent. Acta Polymerica Sinica. 2011;011:1253–1257.
  • Fréchet J, Henmi M, Gitsov I, et al. Self-condensing vinyl polymerization: an approach to dendritic materials. Science. 1995;269:1080–1083.
  • Gaynor S, Edelman S, Matyjaszewski K. Synthesis of branched and hyperbranched polystyrenes. Macromolecules. 1996;29:1079–1081.
  • Matyjaszewski K, Gaynor SG, Kulfan A, et al. Preparation of hyperbranched polyacrylates by atom transfer radical polymerization. 1. Acrylic AB* Monomers in “Living” Radical Polymerizations. Macromolecules. 1997;30:5192–5194.
  • Alfurhood J, Sun H, Bachler P, et al. Hyperbranched poly(N-(2-hydroxypropyl) methacrylamide) via RAFT self-condensing vinyl polymerization. Polym Chem. 2016;7:2099–2104.
  • Baskaran D. Hyperbranched polymers from divinylbenzene and 1,3-diisopropenylbenzene through anionic self-condensing vinyl polymerization. Polymer. 2003;44:2213–2220.
  • Burchard W. Solution properties of branched macromolecules. Adv Polym Sci. 1999;143:114–194.
  • Saunders G, Cormack P, Graham S, et al. Use of rapid triple detection size exclusion chromatography to evaluate the evolution of molar mass and branching architecture during free radical branching copolymerization of methyl methacrylate and ethylene glycol dimethacrylate. Macromolecules. 2005;38:6418–6422.
  • Burchard W, Schmidt M, Stockmayer W. Information on polydispersity and branching from combined quasi-elastic and integrated scattering. Macromolecules. 1980;13:1265–1272.
  • Huang W, Yang H, Xue X, et al. Polymerization behaviors and polymer branching structures in ATRP of monovinyl and divinyl monomers. Polym Chem. 2013;4:3204–3211.
  • Huang W, Gu W, Yang H, et al. Preparation and properties of branched polystyrene through radical suspension polymerization. Polymers. 2017;9:14.
  • Nikos H, Xenidou M, Iatrou H, et al. Well-defined, model long chain branched polyethylene. 1. synthesis and characterization. Macromolecules. 2000;33:2424–2436.
  • ScholteandN TG, Meijerink LJ. Gel permeation chromatography on branched polymers. Br Polym J. 1977;9:133–139.
  • TackxandJ P, Tacx CJF. Chain architecture of LDPE as a function of molar mass using size exclusion chromatography and multi-angle laser light scattering (SEC-MALLS). Polymer. 1998;39:3109–3113.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.