Covalent polymers connected by non-covalent interactions constitute a fascinating set of materials known as supramolecular polymer networks (SPNs). A key feature of SPNs is that the underlying covalent polymers endow the resulting self-assembled materials with features, such as structural and mechanical integrity, good processability, recyclability, stimuli-responsiveness, self-healing, and shape memory, that are not recapitulated in the case of classic covalent polymer systems. The unique nature of SPNs derives from the controlled marriage of traditional covalent polymers and macrocycle-based host−guest interactions. As a consequence, supramolecular polymeric networks have played important roles in a number of diverse fields, including polymer science, supramolecular chemistry, materials science, biomedical materials, and information storage technology. In this Review, we summarize advances made in the area of functional SPNs, with a focus on original literature reports appearing in the past five years. The treatment is organized according to the key macrocycle-based host−guest interactions used to produce various SPNs. The role of the underlying polymer backbones is also discussed.
Macromolecular supra-amphiphiles refer to a kind of macromolecular amphiphiles whose hydrophlic and hydrophobic parts are connected by noncovalent forces. They have applications in various fields, such as drug delivery, sensor systems, and biomedical materials. Here we report a novel molecular recognition motif between a new thermoresponsive water-soluble pillar[7]arene (WP7) and an azobenzene derivative. Furthermore, we utilized this recognition motif to construct the first pillararene-based supra-amphiphilic polypseudorotaxane which can self-assemble to form vesicles in water. Due to the dual-responsiveness of the molecular recognition motif (the thermoresponsiveness of WP7 and photoresponsiveness of azobenzene), the reversible transformations between solid nanospheres based on the self-assembly of the polymer backbone and vesicles based on the self-assembly of the supra-amphiphilic polypseudorotaxane were achieved by adjusting the solution temperature or UV-visible light irradiation. These dual-responsive aggregation behaviors were further used in the controlled release of water-soluble dye calcein molecules.
Here we report the unprecedented preparation of nanoparticles with near-infrared (NIR) emission enhanced by host-guest complexation between a water-soluble pillar[5]arene (WP5) and a cyanostilbene derivative (1) in water. Amphiphilic 1 self-assembles in water to form nanoribbons with relatively weak NIR emission at low concentrations. However, after addition of equimolar WP5, these nanoribbons transform into nanoparticles with stronger NIR emission due to the formation of a supramolecular amphiphile and host-guest complexation-enhanced aggregation. These nanoparticles show pH responsiveness, and collapse after treatment with acid. More importantly, these nanoparticles can be used in living cell imaging.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.