“…In a related vein, and somewhat reminiscent of light‐induced polymer network strand growth (see Section 3.3.4) for network strengthening, the random homolytic cleavage of covalent bonds that occurs upon excessively straining polymer networks has been used to induced network healing via the growth of new polymer strands . Moreover, piezoelectric materials such as zinc oxide or even water, which are capable of generating free radicals in response to low‐amplitude, high‐frequency vibrational forces (e.g., ultrasound), have been used to control polymer growth; this strategy could provide another means to design self‐strengthening networks. In the future, novel mechanophore designs coupled with additive manufacturing strategies will enable the development of novel classes of polymer networks ranging from optimized elastomers to advanced metamaterials …”
Polymer networks, which are materials composed of many smaller components—referred to as “junctions” and “strands”—connected together via covalent or non‐covalent/supramolecular interactions, are arguably the most versatile, widely studied, broadly used, and important materials known. From the first commercial polymers through the plastics revolution of the 20th century to today, there are almost no aspects of modern life that are not impacted by polymer networks. Nevertheless, there are still many challenges that must be addressed to enable a complete understanding of these materials and facilitate their development for emerging applications ranging from sustainability and energy harvesting/storage to tissue engineering and additive manufacturing. Here, we provide a unifying overview of the fundamentals of polymer network synthesis, structure, and properties, tying together recent trends in the field that are not always associated with classical polymer networks, such as the advent of crystalline “framework” materials. We also highlight recent advances in using molecular design and control of topology to showcase how a deep understanding of structure–property relationships can lead to advanced networks with exceptional properties.
“…In a related vein, and somewhat reminiscent of light‐induced polymer network strand growth (see Section 3.3.4) for network strengthening, the random homolytic cleavage of covalent bonds that occurs upon excessively straining polymer networks has been used to induced network healing via the growth of new polymer strands . Moreover, piezoelectric materials such as zinc oxide or even water, which are capable of generating free radicals in response to low‐amplitude, high‐frequency vibrational forces (e.g., ultrasound), have been used to control polymer growth; this strategy could provide another means to design self‐strengthening networks. In the future, novel mechanophore designs coupled with additive manufacturing strategies will enable the development of novel classes of polymer networks ranging from optimized elastomers to advanced metamaterials …”
Polymer networks, which are materials composed of many smaller components—referred to as “junctions” and “strands”—connected together via covalent or non‐covalent/supramolecular interactions, are arguably the most versatile, widely studied, broadly used, and important materials known. From the first commercial polymers through the plastics revolution of the 20th century to today, there are almost no aspects of modern life that are not impacted by polymer networks. Nevertheless, there are still many challenges that must be addressed to enable a complete understanding of these materials and facilitate their development for emerging applications ranging from sustainability and energy harvesting/storage to tissue engineering and additive manufacturing. Here, we provide a unifying overview of the fundamentals of polymer network synthesis, structure, and properties, tying together recent trends in the field that are not always associated with classical polymer networks, such as the advent of crystalline “framework” materials. We also highlight recent advances in using molecular design and control of topology to showcase how a deep understanding of structure–property relationships can lead to advanced networks with exceptional properties.
“…Auf ähnliche Weise – und an das lichtinduzierte Wachstum von Strängen in Polymernetzwerken (siehe Abschnitt 3.3.4) zur Verfestigung von Netzwerken erinnernd – wurde die zufällige homolytische Spaltung von kovalenten Bindungen, die nach übermäßiger Belastung des Polymernetzwerks erfolgt, für die induzierte Selbstheilung des Netzwerks durch das Wachsen neuer Polymerstränge genutzt . Außerdem wurden piezoelektrische Materialien wie Zinkoxid oder selbst Wasser, die freie Radikale als Reaktion auf Schwingungen mit hoher Frequenz und kleiner Amplitude (z. B. Ultraschall) bilden können, zur Steuerung des Polymerwachstums verwendet; diese Strategie könnte eine weitere Möglichkeit zur Entwicklung von selbst‐verfestigenden Netzwerken sein.…”
Section: Struktur Von Polymernetzwerkenunclassified
Polymernetzwerke sind Materialien, die aus vielen kleineren Komponenten aufgebaut sind, die als “Vernetzungspunkte” und “Stränge” bezeichnet werden und über kovalente oder nichtkovalente/supramolekulare Wechselwirkungen miteinander verknüpft sind. Sie gehören zu den vielseitigsten, am häufigsten eingesetzten und wichtigsten Materialien. Von den ersten kommerziellen Polymeren über die Kunststoffrevolution des 20. Jahrhunderts bis in die Gegenwart gibt es nahezu keine Aspekte des modernen Lebens, die nicht von Polymernetzwerken beeinflusst werden. Dennoch müssen noch viele Herausforderungen in Angriff genommen werden, um ein vollständiges Verständnis dieser Materialien zu ermöglichen und ihre Entwicklung für künftige Anwendungen zu fördern, die von Energie‐Harvesting und Energiespeicherung bis zur Gewebezüchtung und additiven Fertigung reichen. Hier geben wir einen Überblick über die Grundlagen der Synthese, Struktur und Eigenschaften von Polymernetzwerken, unter Einbeziehung aktueller Trends auf dem Gebiet. Wir werden außerdem die neuesten Fortschritte bei der Anwendung des Moleküldesigns und der Steuerung der Topologie aufzeigen, um zu demonstrieren, wie ein tiefgehendes Verständnis der Struktur‐Eigenschaft‐Beziehungen zu hochentwickelten Netzwerken mit außergewöhnlichen Eigenschaften führen kann.
“…It can be triggered by the introduction of a reducing compound, for example, radical initiator in initiators for continuous activator regeneration (ICAR) ATRP, chemical reducing agents (e.g., glucose, ascorbic acid, hydrazine), and metallic silver in activators regenerated by electron transfer (ARGET) ATRP, zerovalent metals (Fe 0 , Cu 0 ) in supplemental activator and reducing agent (SARA) ATRP. Alternatively, an external stimuli such as a reducing current in electrochemically mediated ATRP ( e ATRP) and simplified electrochemically mediated ATRP ( se ATRP), light in photo‐induced ATRP (photo‐ATRP), or mechanical forces in mechanically induced ATRP (mechano‐ATRP) and in ultrasonication‐induced ATRP (sono‐ATRP) can be applied . Electrochemistry offers additional opportunity to catalyst recycle, eliminates needs for chemical reducing agents, provides temporal control during the process, and extends polymerization to aqueous media .…”
A vitamin‐B2‐based macroinitiator is prepared by esterification of riboflavin with 2‐bromoisobutyryl bromide. Following the “core first” methodology, “phoenix”‐shape (co)polymers with a polar riboflavin core and either a hydrophobic (poly(n‐butyl acrylate) or poly(methyl methacrylate)) or hydrophilic (poly(N‐isopropylacrylamide)‐block‐poly(oligo(ethylene glycol) acrylate) or poly(N‐isopropylacrylamide)‐block‐poly(2‐hydroxyethyl acrylate)) tails are synthesized via low ppm atom transfer radical polymerization procedures. Polymers have predetermined molecular weights and a low dispersity (Ð < 1.2). 1H NMR analysis confirms the successful formation of targeted (co)polymers with the preserved riboflavin functionality.
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