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The rise of azide-alkyne 1,3-dipolar 'click' cycloaddition and its application to polymer science and surface modification

Journal

AUSTRALIAN JOURNAL OF CHEMISTRY
Volume 60, Issue 6, Pages 384-395

Publisher

CSIRO PUBLISHING
DOI: 10.1071/CH06457

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New methods to synthesize and functionalize polymers are of constant interest to the polymer scientist. The 1,3-dipolar cycloaddition between an azide and terminal alkyne has received much attention since the reports that copper(I) provides high yields and regioselective synthesis of 1,4-substituted 1,2,3-triazoles. This coupling chemistry has been rapidly adopted by polymer scientists in the synthesis and post-polymerization modification of polymers. This Review will provide the historical context of the recent development of the copper-mediated azide - alkyne cycloaddition and its use in polymer science, particularly in dendrimer synthesis/functionalization, surface immobilization/modification, orthogonally functionalizing polymers, and its integration with ATRP ( atom transfer radical polymerization).

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