We have prepared polyion complex (PIC) hydrogel consisting of poly(3-(methacryloylami no)propyl-trimethylamonium chloride) and poly(sodium p-styrenesulfonate) polyelectrolytes via a two-step polymerization pro...We have prepared polyion complex (PIC) hydrogel consisting of poly(3-(methacryloylami no)propyl-trimethylamonium chloride) and poly(sodium p-styrenesulfonate) polyelectrolytes via a two-step polymerization procedure and have investigated specific ion effects on the self- healing of the PIC hydrogel. Our study demonstrates that the mechanical properties of the PIC hydrogel are strongly dependent on the type of the ions doped in the hydrogel. The ion-specific effects can be used to modulate the self-healing efficiency of the PIC hydrogel. As the doped anions change from kosmotrops to chaotropes, the self-healing efficiency of the PIC hydrogel increases. A more chaotropic anion has a stronger ability to break the ionic bonds formed within the hydrogel, leading to a higher efficiency during the healing.展开更多
A novel synthetic strategy towards pH-responsive aggregation-induced emission (AIE)-active tetraphenylethene (TPE)- functionalized polyethylene-based block copolymers is presented. Tris(3-(4-(l,2,2-triphenylvinyl)phen...A novel synthetic strategy towards pH-responsive aggregation-induced emission (AIE)-active tetraphenylethene (TPE)- functionalized polyethylene-based block copolymers is presented. Tris(3-(4-(l,2,2-triphenylvinyl)phenoxy)propyl)borane was used to initiate the polyhomologation of dimethylsulfoxonium methylide to afford well-defined a-TPE-ω-OH linear polyethylenes (PE). The terminal hydroxyl groups were transformed to atom transfer radical polymerization (ATRP) initiating sites by esterification with bromoisobutyryl bromide, followed by polymerization of rert-butyl acrylate (tBA) to provide TPE-PE-b-PtBA block copolymers. After hydrolysis of the rBu group to COOH group, the corresponding pH-responsive TPE-PE-b-PAA block copolymers were obtained. All synthesized block copolymers revealed AIE behavior either in solution or bulk. Due to the pH-responsivity of PAA chains, the aggregation state at different pH and consequently the fluorescence intensity changed. Also, the synthesized block copolymers exhibited ion-specificity fluorescence properties.展开更多
Since the discovery of biological ion channels and their role in physiology,scientists have been trying to create artificial structures that mimic biological ion channels.Nanochannels such as biological/solid-state na...Since the discovery of biological ion channels and their role in physiology,scientists have been trying to create artificial structures that mimic biological ion channels.Nanochannels such as biological/solid-state nanopores and porous nanostructures can have fine-tuned ion behaviors in a confined space where ions are“aggregated”.Thus,one of the most exciting applications of nanochannels is artificial neurons and neural network based on the ion-specific effects and nanofluidics.In this review article,it is the first time that the ion aggregation behaviors inside the confined nanochannels are summarized,and their connection to neuroscience,especially the artificial neurons and neural network,is explored and envisioned.展开更多
文摘We have prepared polyion complex (PIC) hydrogel consisting of poly(3-(methacryloylami no)propyl-trimethylamonium chloride) and poly(sodium p-styrenesulfonate) polyelectrolytes via a two-step polymerization procedure and have investigated specific ion effects on the self- healing of the PIC hydrogel. Our study demonstrates that the mechanical properties of the PIC hydrogel are strongly dependent on the type of the ions doped in the hydrogel. The ion-specific effects can be used to modulate the self-healing efficiency of the PIC hydrogel. As the doped anions change from kosmotrops to chaotropes, the self-healing efficiency of the PIC hydrogel increases. A more chaotropic anion has a stronger ability to break the ionic bonds formed within the hydrogel, leading to a higher efficiency during the healing.
基金supported by King Abdullah University of Science and Technology (KAUST)
文摘A novel synthetic strategy towards pH-responsive aggregation-induced emission (AIE)-active tetraphenylethene (TPE)- functionalized polyethylene-based block copolymers is presented. Tris(3-(4-(l,2,2-triphenylvinyl)phenoxy)propyl)borane was used to initiate the polyhomologation of dimethylsulfoxonium methylide to afford well-defined a-TPE-ω-OH linear polyethylenes (PE). The terminal hydroxyl groups were transformed to atom transfer radical polymerization (ATRP) initiating sites by esterification with bromoisobutyryl bromide, followed by polymerization of rert-butyl acrylate (tBA) to provide TPE-PE-b-PtBA block copolymers. After hydrolysis of the rBu group to COOH group, the corresponding pH-responsive TPE-PE-b-PAA block copolymers were obtained. All synthesized block copolymers revealed AIE behavior either in solution or bulk. Due to the pH-responsivity of PAA chains, the aggregation state at different pH and consequently the fluorescence intensity changed. Also, the synthesized block copolymers exhibited ion-specificity fluorescence properties.
基金Natural Science Foundation of China,Grant/Award Number:22102029Natural Science Foundation of Fujian Province,Grant/Award Number:2021J01158。
文摘Since the discovery of biological ion channels and their role in physiology,scientists have been trying to create artificial structures that mimic biological ion channels.Nanochannels such as biological/solid-state nanopores and porous nanostructures can have fine-tuned ion behaviors in a confined space where ions are“aggregated”.Thus,one of the most exciting applications of nanochannels is artificial neurons and neural network based on the ion-specific effects and nanofluidics.In this review article,it is the first time that the ion aggregation behaviors inside the confined nanochannels are summarized,and their connection to neuroscience,especially the artificial neurons and neural network,is explored and envisioned.