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