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Australian Journal of Chemistry
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The Rise of Azide–Alkyne 1,3-Dipolar ‘Click’ Cycloaddition and its Application to Polymer Science and Surface Modification

Richard A. Evans

A CSIRO Molecular and Health Technologies, Bag 10, Clayton South VIC 3169, Australia. Email: richard.evans@csiro.au
B Centre for Advanced Macromolecular Design (CAMD), School of Chemical Engineering and Industrial Chemistry, University of New South Wales, Sydney NSW 2052, Australia.


Abstract

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).

Australian Journal of Chemistry 60(6) 384–395    doi:10.1071/CH06457
Submitted: 1 December 2006    Accepted: 24 January 2007    Published: 18 June 2007





   
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