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 …

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

A novel mussel-inspired sticky catechol-functionalized poly (ethylene glycol)(Cate-PEG) was
synthesized and deployed as an additive to modify the hydrophobic poly (vinylidene …

This year, it has been a decade that the concept of “click” chemistry was pioneered in
polymer and material science by the exploration of the synthetic scope of copper-catalyzed …

Conventional chemically cross-linked double network hydrogels (DN hydrogels) are
considered as one of the toughest soft materials. However, they lack self-healing properties …

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 …

Polyamides with various functional side groups were synthesized via Passerini reaction in a
one-pot approach. The polymerization conditions and kinetics as well as the resulting …

Here we demonstrate a type of pH and reduction dual-sensitive biodegradable micelles,
which were self-assembled by a cationic polymer in an aqueous solution. Due to tumor cells …

In this study, we probe various aspects of a post-polymerization double-modification strategy
involving sequential thiol–epoxy and esterification reactions for the preparation of dual …

Orthogonal, sequential “click” reactions were implemented to yield novel polymeric
substrates with the ability to record holographic data. The base-catalyzed thiol–acrylate …