{"title":"N-Sulfonyl Guanidine Urea to Design Ultrastrong, Stable, and Recyclable Associative Dynamic Polyurea Networks","authors":"Zhen Yu, Yanlin Liu, Sheng Wang, Yajin Fang, Xiangyu Zhou, Zhaobin Tang, Jin Zhu, Junping Zhang","doi":"10.1021/acs.macromol.4c01575","DOIUrl":null,"url":null,"abstract":"Dynamic covalent adaptive networks can solve the recycling issue of thermosets. However, dissociative dynamic covalent networks may suffer from instability and network incompleteness at high temperatures or in solvents. Here, we report a novel dynamic covalent bond, <i>N</i>-sulfonyl guanidine urea (SGUA), that can undergo catalyst-free metathesis reactions, in which a passivation strategy of increasing the dissociation temperature of guanidine urea by introducing electron-withdrawing <i>N</i>-sulfonyl groups into adjacent positions was developed. Unlike conventional dissociative dynamic urea bonds, SGUAs exhibit associative metathesis reactions at around 120–180 °C, with a high dissociation threshold of 180 °C. The dynamic covalent polyurea constructed by SGUAs, named PSGUAs, exhibits ultrastrong (Young’s modulus exceeding 4 GPa and tensile strength exceeding 60 MPa) and stable (thermal stability, network structure integrity under reprocessing, and dimensional stability) performances. Furthermore, due to the excellent dynamic characteristics of SGUAs, PSGUAs were successfully reprocessed after 30–60 min of hot pressing at 160 °C and 20 MPa. Combining the long-lasting antibacterial properties of PSGUAs with long-term use, this study marks a substantial improvement in the field of dynamic polymer networks, giving a solution for balancing material stability, high performance, and reprocessability.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"42 1","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2024-11-20","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.4c01575","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Dynamic covalent adaptive networks can solve the recycling issue of thermosets. However, dissociative dynamic covalent networks may suffer from instability and network incompleteness at high temperatures or in solvents. Here, we report a novel dynamic covalent bond, N-sulfonyl guanidine urea (SGUA), that can undergo catalyst-free metathesis reactions, in which a passivation strategy of increasing the dissociation temperature of guanidine urea by introducing electron-withdrawing N-sulfonyl groups into adjacent positions was developed. Unlike conventional dissociative dynamic urea bonds, SGUAs exhibit associative metathesis reactions at around 120–180 °C, with a high dissociation threshold of 180 °C. The dynamic covalent polyurea constructed by SGUAs, named PSGUAs, exhibits ultrastrong (Young’s modulus exceeding 4 GPa and tensile strength exceeding 60 MPa) and stable (thermal stability, network structure integrity under reprocessing, and dimensional stability) performances. Furthermore, due to the excellent dynamic characteristics of SGUAs, PSGUAs were successfully reprocessed after 30–60 min of hot pressing at 160 °C and 20 MPa. Combining the long-lasting antibacterial properties of PSGUAs with long-term use, this study marks a substantial improvement in the field of dynamic polymer networks, giving a solution for balancing material stability, high performance, and reprocessability.
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.