English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Zendy Open

Presents the pdf analysis as premium feature

PDF Analysis

Insights

Presents the summarisation as premium feature

Summarisation

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the zaia usage as premium feature

ZAIA

Zendy Tools

Zendy Plus

Presents the access of premium content as premium feature

Premium Content

Within the last few years, crystallisation-induced self-assembly of block copolymers (BCs) in solution has become more and more attractive for the production of well-defined cylindrical crystalline-core micelles (cCCMs). The “livingness” of this process has been shown for a number of crystallisable blocks and allows fine tuning of the length as well as the length distribution of such structures. This unprecedented control is hardly achievable in the self-assembly of purely amorphous BCs. Furthermore, in an analogy to living/controlled polymerisation methods, the epitaxial growth of different BCs onto preformed cCCMs allows for the preparation of complex micellar architectures, e.g., cylindrical block co-micelles. This highlight tries to provide an overview over recent developments in crystallisation-induced self-assembly of BCs with a particular focus on one-dimensional (1D) micellar nanostructures.

Cylindrical crystalline-core micelles: pushing the limits of solution self-assembly