'Click' Chemistry in Polymer and Material Science: An Update

The metal catalyzed azide/alkyne ‘click’ reaction (a variation of the Huisgen 1,3‐dipolar cycloaddition reaction between terminal acetylenes and azides) has vastly increased in broadness and application in the field of polymer science. Thus, this reaction represents one of the few universal, highly...

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Published inMacromolecular rapid communications. Vol. 29; no. 12-13; pp. 952 - 981
Main Authors Binder, Wolfgang H., Sachsenhofer, Robert
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.07.2008
WILEY‐VCH Verlag
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Summary:The metal catalyzed azide/alkyne ‘click’ reaction (a variation of the Huisgen 1,3‐dipolar cycloaddition reaction between terminal acetylenes and azides) has vastly increased in broadness and application in the field of polymer science. Thus, this reaction represents one of the few universal, highly efficient functionalization reactions, which combines both high efficiency with an enormously high tolerance of functional groups and solvents under highly moderate reaction temperatures (25–70 °C). The present review assembles an update of this reaction in the field of polymer science (linear polymers, surfaces) with a focus on the synthesis of functionalized polymeric architectures and surfaces.
Bibliography:ark:/67375/WNG-WW7N49ML-7
istex:D0000A0F4E2245B5B6F4C8F5AF45D927B1AF234E
FWF - No. 18740 B03
ArticleID:MARC200800089
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:1022-1336
1521-3927
DOI:10.1002/marc.200800089