Stimulus-responsive block copolymer nano-objects and hydrogels via dynamic covalent chemistry.

Stimulus-responsive block copolymer nano-objects and hydrogels via dynamic covalent chemistry† †Electronic supplementary information (ESI) available: GPC date, additional TEM images and DLS data. See DOI: 10.1039/c7py01242j

Using Dynamic Covalent Chemistry To Drive Morphological Transitions: Controlled Release of Encapsulated Nanoparticles from Block Copolymer Vesicles

Dynamic covalent chemistry is exploited to drive morphological order-order transitions to achieve the controlled release of a model payload (e.g., silica nanoparticles) encapsulated within block copolymer vesicles. More specifically, poly(glycerol monomethacrylate)-poly(2-hydroxypropyl methacrylate) (PGMA-PHPMA) diblock copolymer vesicles were prepared via aqueous polymerization-induced self-as...

Polymerization-Induced Self-Assembly of Block Copolymer Nano-objects via RAFT Aqueous Dispersion Polymerization

In this Perspective, we discuss the recent development of polymerization-induced self-assembly mediated by reversible addition-fragmentation chain transfer (RAFT) aqueous dispersion polymerization. This approach has quickly become a powerful and versatile technique for the synthesis of a wide range of bespoke organic diblock copolymer nano-objects of controllable size, morphology, and surface f...

Multi-responsive and tough hydrogels based on triblock copolymer micelles as multi-functional macro-crosslinkers.

Multi-stimuli responsive hydrogels are synthesized using self-assembled nanomicelles of Pluronic F127 diacrylate triblock copolymer as non-covalent macro-crosslinkers to in situ copolymerize with acrylamide and methyl chloride quaternized N,N-dimethylamino ethylacrylate monomers, generating positively charged hydrogels. These hydrogels showed high strength, toughness, and outstanding fatigue re...

Multifunctional periodic mesoporous organosilicas with bridging groups formed via dynamic covalent chemistry.

Imine-containing bridging groups were formed during self-assembly of periodic mesoporous organosilicas by in situ dynamic covalent chemistry of aldehyde and amine groups in the presence of poly(ethylene oxide)-poly(dl-lactic acid-co-glycolic acid)-poly(ethylene oxide) block copolymer in acidic aqueous solutions.