Synthesis and postpolymerization functionalization of poly(5-iodo-1,2,3- triazole)s

Erik Schwartz, Kurt Breitenkamp, Valery V. Fokin

Результат исследований: Материалы для журналаСтатьярецензирование

57 Цитирования (Scopus)

Аннотация

The step-growth, click polymerization of complementary azide and alkyne-containing monomers to produce polytriazoles (PTAs) has become a versatile and popular method of preparing structurally diverse high molecular weight polymers with a variety of useful functions. We describe here a new class of PTAs that contain 5-iodotriazole linkages prepared by the iodoalkyne version of the copper-catalyzed azide-alkyne cycloaddition (iCuAAC) of an α-azido-ω-iodoalkyne (A-B) monomer. We found this monomer to be highly reactive in the iCuAAC polymerization and show that the resulting poly(5-iodo-1,2,3-triazole) (iodo-PTA) can serve as a useful building block for further postpolymerization derivatization using palladium-catalyzed cross-couplings such as Suzuki and Heck reactions. The parent iodo-PTA and functionalized materials were successfully characterized by various spectroscopic techniques and shown to exhibit a wide range of chemical and thermal properties that are determined by the nature of functionalization at the 5-position of the triazole ring. This data suggests a certain tunability of PTA properties and offers potential for the development of a multitude of useful triazole-based materials based on this postpolymerization functionalization strategy.

Язык оригиналаАнглийский
Страницы (с-по)4735-4741
Число страниц7
ЖурналMacromolecules
Том44
Номер выпуска12
DOI
СостояниеОпубликовано - 28 июн 2011
Опубликовано для внешнего пользованияДа

ASJC Scopus subject areas

  • Organic Chemistry
  • Materials Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry

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