{"title":"具有增强稳定性的原位交联辅助聚合诱导聚合物立方体自组装","authors":"Yalan Sun, Tianhao Chen, Yongbin Zhao, Aihua Chen","doi":"10.1021/acs.macromol.5c01526","DOIUrl":null,"url":null,"abstract":"Polymer cubosomes (PCs) are promising porous materials, but suffer from unstable structures under harsh chemical conditions. Herein, we report a robust “shaping-isolating-cross-linking” strategy that combines polymerization-induced self-assembly (PISA) with sequential separation and then in situ cross-linking to enhance the stability of polystyrene-based (PS-based) PCs. Taking poly(hydroxypropyl methacrylate) (PHPMA) as the stabilizer, PS-based PCs were first synthesized via reversible addition–fragmentation chain transfer (RAFT) polymerization-mediated PISA in ethanol, yielding well-defined <i>Im</i>3̅<i>m</i> bicontinuous structures. Subsequently, these PCs were isolated from the PISA system and then used as seeds to fabricate cross-linked PCs using divinylbenzene (DVB) as the cross-linker by RAFT dispersion polymerization. The cross-linked PCs preserved their original bicontinuous morphologies, and their resistance to organic solvents and high temperatures was significantly enhanced. This approach can be applied to systems with stabilizers containing pyridine groups and cross-linkers involving disulfide bonds, exhibiting recyclable catalytic and stimuli-responsive performances in organic solvents, respectively. We believe that this work establishes a scalable platform for stabilizing complex porous morphologies and broadening their applications.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"18 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolated In Situ Cross-Linking-Assisted Polymerization-Induced Self-Assembly to Polymer Cubosomes with Enhanced Stability\",\"authors\":\"Yalan Sun, Tianhao Chen, Yongbin Zhao, Aihua Chen\",\"doi\":\"10.1021/acs.macromol.5c01526\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Polymer cubosomes (PCs) are promising porous materials, but suffer from unstable structures under harsh chemical conditions. Herein, we report a robust “shaping-isolating-cross-linking” strategy that combines polymerization-induced self-assembly (PISA) with sequential separation and then in situ cross-linking to enhance the stability of polystyrene-based (PS-based) PCs. Taking poly(hydroxypropyl methacrylate) (PHPMA) as the stabilizer, PS-based PCs were first synthesized via reversible addition–fragmentation chain transfer (RAFT) polymerization-mediated PISA in ethanol, yielding well-defined <i>Im</i>3̅<i>m</i> bicontinuous structures. Subsequently, these PCs were isolated from the PISA system and then used as seeds to fabricate cross-linked PCs using divinylbenzene (DVB) as the cross-linker by RAFT dispersion polymerization. The cross-linked PCs preserved their original bicontinuous morphologies, and their resistance to organic solvents and high temperatures was significantly enhanced. This approach can be applied to systems with stabilizers containing pyridine groups and cross-linkers involving disulfide bonds, exhibiting recyclable catalytic and stimuli-responsive performances in organic solvents, respectively. We believe that this work establishes a scalable platform for stabilizing complex porous morphologies and broadening their applications.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.macromol.5c01526\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c01526","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Isolated In Situ Cross-Linking-Assisted Polymerization-Induced Self-Assembly to Polymer Cubosomes with Enhanced Stability
Polymer cubosomes (PCs) are promising porous materials, but suffer from unstable structures under harsh chemical conditions. Herein, we report a robust “shaping-isolating-cross-linking” strategy that combines polymerization-induced self-assembly (PISA) with sequential separation and then in situ cross-linking to enhance the stability of polystyrene-based (PS-based) PCs. Taking poly(hydroxypropyl methacrylate) (PHPMA) as the stabilizer, PS-based PCs were first synthesized via reversible addition–fragmentation chain transfer (RAFT) polymerization-mediated PISA in ethanol, yielding well-defined Im3̅m bicontinuous structures. Subsequently, these PCs were isolated from the PISA system and then used as seeds to fabricate cross-linked PCs using divinylbenzene (DVB) as the cross-linker by RAFT dispersion polymerization. The cross-linked PCs preserved their original bicontinuous morphologies, and their resistance to organic solvents and high temperatures was significantly enhanced. This approach can be applied to systems with stabilizers containing pyridine groups and cross-linkers involving disulfide bonds, exhibiting recyclable catalytic and stimuli-responsive performances in organic solvents, respectively. We believe that this work establishes a scalable platform for stabilizing complex porous morphologies and broadening their applications.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.