Click chemistry is one of the most powerful strategies for constructing polymeric soft
materials with precise control over architecture and functionality. In this review, we provide a …

Thiyl radicals have been used by nature in a broad range of biochemical processes. For
instance, thiol residues play an important role in many enzymatic processes as illustrated by …

The translation of small molecule chemistries into efficient methodologies for polymer
functionalization spans several decades, enabling critical advances in soft matter materials …

Despite originating only a little more than a decade ago, click chemistry has become one of
the most powerful paradigms in materials science, synthesis, and modification. By …

Post-polymerisation modification of poly (glycidyl methacrylate)(PGMA) through the
nucleophilic ring opening reactions of the pendent epoxide groups allows for the installation …

This chapter highlights the current status of critically selected post‐functionalization
techniques of polymers via orthogonal ligation chemistry, reports the major characteristics of …

Base‐catalyzed reaction between a thiol and an epoxide group is a simple fusion process
that leads to the formation of a β‐hydroxythio‐ether linkage. This reaction is efficient, regio …

In the last decade, interest in the functionalization of surfaces and materials has increased
dramatically. In this regard, click chemistry deserves a central focus because of its mild …

Polymer brushes present a unique architecture for tailoring surface functionalities due to
their distinctive physicochemical properties. However, the polymerization chemistries used …

Over the last decade, click chemistry reactions, that are fast, simple to use, easy to purify,
versatile, regiospecific, and give high product yields have gained significant importance for …