Nie, J.; Yin, H.; Cao, R.; Huang, C.; Luo, X.; Ji, J. Responsive Microgels through RAFT-HDA Dynamic Covalent Bonding Chemistry. Molecules2024, 29, 1217.
Nie, J.; Yin, H.; Cao, R.; Huang, C.; Luo, X.; Ji, J. Responsive Microgels through RAFT-HDA Dynamic Covalent Bonding Chemistry. Molecules 2024, 29, 1217.
Nie, J.; Yin, H.; Cao, R.; Huang, C.; Luo, X.; Ji, J. Responsive Microgels through RAFT-HDA Dynamic Covalent Bonding Chemistry. Molecules2024, 29, 1217.
Nie, J.; Yin, H.; Cao, R.; Huang, C.; Luo, X.; Ji, J. Responsive Microgels through RAFT-HDA Dynamic Covalent Bonding Chemistry. Molecules 2024, 29, 1217.
Abstract
In this paper, a method for the preparation of ultrasound-responsive microgels was developed based on RAFT-HDA dynamic covalent bonding. First, a styrenic cross-linked network was suc-cessfully prepared by DA reaction between phosphoryl dithioester and furan using double-ended BDEPDF as RAFT reagent mediated St polymerization as double-ended dienophile linker and co-polymer of FMA and St as dienophile. Subsequently, the microgel system was constructed by the HDA reaction between phosphoryl disulfide and furan groups using the copolymer of polyethylene glycol monomethyl ether acrylate (OEGMA) and FMA as the dienophore building block and hy-drophilic segment, and the polystyrene pro-dienophile linker as the cross-linker and hydrophobic segment. The number of furans in the dienophile chain and the length of the dienophile linker were regulated by RAFT polymerization to investigate the effects of single-molecule chain functional group degree (f), furan/dithioester ratio (r), and hydrophobic linker length (D) on the microgel system. These microgels can achieve the reversible transformation of materials under force re-sponsiveness, and the steps are simple and adaptive, which are expected to show important po-tential applications in the fields of biomedical materials and adaptive electrical materials.
Chemistry and Materials Science, Materials Science and Technology
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