The “click” chemistry concept is based on utilizing rapid reactions which are efficient,
versatile, and selective. Indeed, Diels–Alder (DA) reactions fulfill most of the requirements …

Anthracene, with its unique properties originating from the linearly fused benzene ring
structure, has a long history in polymer science in numerous application areas. The most …

Double click reaction strategies, which are a combination of different type of click reactions,
allow the preparation of polymers with various topologies and the post-functionalization of …

Functional polymeric materials with desired properties can be designed by precise control of
macromolecular architectures. Over the recent years, click reactions have enabled efficient …

Branched polymers result in a more compact structure in comparison to linear polymers of
identical molecular weight, due to their high segment density which affects the crystalline …

This mini‐review provides an introduction to the key work in the area of synthesis and post‐
polymerization functionalization of maleimide‐functional polymers. The versatility and utility …

Abstract This Feature Article focuses on the rapidly emerging concept of the “triple click
reactions” towards the design and synthesis of macromolecules with well‐defined topology …

A strategy for the modular ambient temperature synthesis of ABA and ABC triblock
copolymers via a combination of photoinduced Diels–Alder reactions with thermal Diels …

Polymers bearing the dibromomaleimide (DBM) group as a functional chain end have been
synthesized by RAFT polymerization. A DBM functional chain transfer agent (CTA) was …

Abstract Azide‐alkyne and Diels–Alder click reactions together with a click‐like nitroxide
radical coupling reaction were used in a one‐pot fashion to generate tetrablock …