4.5 Article

Direct azidation of isotactic polypropylene and synthesis of grafted to' derivatives thereof using azide-alkyne cycloaddition chemistry

Journal

POLYMER INTERNATIONAL
Volume 66, Issue 1, Pages 70-76

Publisher

WILEY-BLACKWELL
DOI: 10.1002/pi.5180

Keywords

azide; post-polymerization modification; polypropylene; hypervalent iodine; cycloaddition chemistry

Funding

  1. Camille Dreyfus Teacher-Scholar Awards Program
  2. US Army Research Office [W911NF-09-1-0446, W911NF-09-1-0456]
  3. National Science Foundation [CHE-1266323]
  4. BK21 Plus Program - Ministry of Education and the National Research Foundation of Korea
  5. IBS [IBS-R019-D1]
  6. Ministry of Science & ICT (MSIT), Republic of Korea [IBS-R019-D1-2017-A00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Azido-functionalized isotactic polypropylene was prepared via the direct CH azidation of a commercially available polymer using a stable azidoiodinane. Including imidazole or benzimidazole in the reaction mixture was found to significantly improve the yields of the post-polymerization modification. Although chain cleavage was observed, the methodology afforded high-molecular-weight (M-w>100 kDa) functionalized polypropylene containing up to 3mol% of azido groups and enabled access to polypropylene-graft-poly(ethylene glycol) copolymers via azide-alkyne cycloaddition chemistry. (c) 2016 Society of Chemical Industry

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