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2.6.4 Polymer Conjugation on Surfaces

DOI: 10.1055/sos-SD-235-00101

Zhang, C.; Page, K. M.; van Hest, J. C. M.Science of Synthesis: Click Chemistry, (20211281.

Chaikof and co-workers were the first to demonstrate a Diels–Alder reaction followed by a CuAAC click reaction between carbohydrates/proteins and glass surfaces.[‌148‌] This study showed the potential of these sequential reactions for the immobilization of an extensive range of intricate structures onto solid surfaces.[‌149‌,‌150‌] Not only can such solid surfaces be adorned, but polymer backbones and thin films can also be decorated with complex structures through CuAAC-assisted postpolymerization modification.[‌151‌] Since polymer backbone functionalization has been discussed in previous sections, the focus here is on polymer thin films, which are used to design robust, nano- and microstructured surfaces.[‌152‌‌154‌] CuAAC modification of polymer interfaces allows the chemical composition and conformation of the attached polymer chains to be efficiently spatially and temporally controlled.[‌151‌,‌155‌] This grants accurate control over interfacial characteristics such as wettability, adherence, friction, and capture of biomolecules.[‌153‌‌155‌] There are multiple ways to functionalize polymers, e.g. using thiols, azlactones, activated esters, and/or azides. Azides are especially effective for functionalizing polymer coatings because of their high stability.[‌144‌,‌145‌,‌156‌]

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