Synthesis of graft copolymers with 'V-shaped' and 'Y-shaped' side chains via controlled radical and anionic polymerizations
Autor: | Yuliang Yang, Xiaojun Wang, Junpo He, Guangzheng Gao, Fengping Yu |
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Rok vydání: | 2007 |
Předmět: |
Nitroxide mediated radical polymerization
Living free-radical polymerization Anionic addition polymerization Polymers and Plastics Polymerization Chemistry Organic Chemistry Polymer chemistry Radical polymerization Materials Chemistry Copolymer Reversible addition−fragmentation chain-transfer polymerization Living anionic polymerization |
Zdroj: | Journal of Polymer Science Part A: Polymer Chemistry. 45:4013-4025 |
ISSN: | 1099-0518 0887-624X |
DOI: | 10.1002/pola.22155 |
Popis: | A combination of nitroxide-mediated radical polymerization and living anionic polymerization was used to synthesize a series of well-defined graft (co)polymers with “V-shaped” and “Y-shaped” branches. The polymer main chain is a copolymer of styrene and p-chloromethylstyrene (PS-co-PCMS) prepared via nitroxide-mediated radical polymerization. The V-shaped branches were prepared through coupling reaction of polystyrene macromonomer, carrying 1,1-diphenylethylene terminus, with polystyryllithium or polyisoprenyllithium. The Y-shaped branches were prepared throughfurther polymerization initiated by the V-shaped anions. The obtained branches, carrying a living anion at the middle (V-shaped) or at the end of the third segment (Y-shaped), were coupled in situ with pendent benzyl chloride of PS-co-PCMS to form the target graft (co)polymers. The purified graft (co)polymers were analyzed by size exclusion chromatography equipped with a multiangle light scattering detector and a viscometer. The result shows that the viscosities and radii of gyration of the branched polymers are remarkably smaller than those of linear polystyrene. In addition, V-shaped product adopts a more compact conformation in dilute solution than the Y-shaped analogy. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4013–4025, 2007 |
Databáze: | OpenAIRE |
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