Abstract:Supramolecular hydrogels are expected to have applications as novel soft materials in various fields owing to their designable functional properties. Herein, we developed an in situ synthesis of supramolecular hydrogelators, which can trigger gelation of an aqueous solution without the need for temperature change. This was achieved by mixing two precursors, which induced the synthesis of a supramolecular gelator and its instantaneous self-assembly into nanofibers. We then performed the in situ synthesis of thi… Show more
“…The confocal laser scanning microscopy (CLSM) technique has drawn great attention due to its high sensitivity and three-dimensional and real-time observation characteristics . These advantages of CLSM imaging have made it a promising technique in exploring the micro-/macrostructure of materials and monitoring the dynamic process of molecular self-assembly and biological events. − In this contribution, we present an early-stage visualization (ESV) technique for the aging process of polypropylene (PP) by the CLSM technique (Figure ). Hydroxyl groups from the oxidation of the C–C bond in polymer backbones were taken as an indicator for aging evolution.…”
Monitoring the evolution of polymer aging, especially early-stage aging, over both time and dimensionality can provide in-depth insight into aging-induced material invalidation and even disastrous accidents. However, it remains a great challenge because currently available methods for polymer aging only provide statistic results at a macroscopic scale. Herein, we report the first three-dimensional early-stage visualization (ESV) technique of polymer aging by using the fluorophore-bonded boronic acid to specifically target aging-induced hydroxyl groups through the B−O click reaction. This method can identify the initial aging of polypropylene (PP) as early as 20.0 min. In contrast, no signals can be detected by conventional infrared spectroscopy even after 21 days of thermal treatment. More importantly, the three-dimensional evolution for early-stage polymer aging was demonstrated: faster aggression in the horizontal plane (4.1 × 10 −4 s −1 ) than in the vertical direction (2.6 × 10 −9 m s −1 ) for PP films. The approach could undoubtedly provide valuable information in elucidating mechanistic details of polymer aging in threedimensional scale and assessing the utility of advanced antiaging materials.
“…The confocal laser scanning microscopy (CLSM) technique has drawn great attention due to its high sensitivity and three-dimensional and real-time observation characteristics . These advantages of CLSM imaging have made it a promising technique in exploring the micro-/macrostructure of materials and monitoring the dynamic process of molecular self-assembly and biological events. − In this contribution, we present an early-stage visualization (ESV) technique for the aging process of polypropylene (PP) by the CLSM technique (Figure ). Hydroxyl groups from the oxidation of the C–C bond in polymer backbones were taken as an indicator for aging evolution.…”
Monitoring the evolution of polymer aging, especially early-stage aging, over both time and dimensionality can provide in-depth insight into aging-induced material invalidation and even disastrous accidents. However, it remains a great challenge because currently available methods for polymer aging only provide statistic results at a macroscopic scale. Herein, we report the first three-dimensional early-stage visualization (ESV) technique of polymer aging by using the fluorophore-bonded boronic acid to specifically target aging-induced hydroxyl groups through the B−O click reaction. This method can identify the initial aging of polypropylene (PP) as early as 20.0 min. In contrast, no signals can be detected by conventional infrared spectroscopy even after 21 days of thermal treatment. More importantly, the three-dimensional evolution for early-stage polymer aging was demonstrated: faster aggression in the horizontal plane (4.1 × 10 −4 s −1 ) than in the vertical direction (2.6 × 10 −9 m s −1 ) for PP films. The approach could undoubtedly provide valuable information in elucidating mechanistic details of polymer aging in threedimensional scale and assessing the utility of advanced antiaging materials.
“…Recently,s upramolecular polymers have also been fabricated by interfacial polymerization of the two precursors in two immiscible solvents,t hereby providing af acile strategy for supramolecular materials with controllable properties,structures,and functions. [37] Coordination polymers,w hich consist of metal ions and organic ligands linked through coordination bonds,appeared in the early 1960s, [38] and the term "coordination polymer" was defined by Bailar in 1964. [39] Acoordination polymer with reversible coordination bonds can also be assigned as as upramolecular polymer.…”
Section: History Of Interfacial Polymerizationmentioning
Interfacial polymerization, where a chemical reaction is confined at the liquid–liquid or liquid–air interface, exhibits a strong advantage for the controllable fabrication of films, capsules, and fibers for use as separation membranes and electrode materials. Recent developments in technology and polymer chemistry have brought new vigor to interfacial polymerization. Here, we consider the history of interfacial polymerization in terms of the polymerization types: interfacial polycondensation, interfacial polyaddition, interfacial oxidative polymerization, interfacial polycoordination, interfacial supramolecular polymerization, and some others. The accordingly emerging functional materials are highlighted, as well as the challenges and opportunities brought by new technologies for interfacial polymerization. Interfacial polymerization will no doubt keep on developing and producing a series of fascinating functional materials.
“…Seit kurzem werden supramolekulare Polymere auch durch Grenzflächenpolymerisation von zwei Precursoren in zwei nicht mischbaren Lçsungsmitteln hergestellt, was eine einfache Herstellung von supramolekularen Materialien mit kontrollierbaren Eigenschaften, Strukturen und Funktionen ermçglicht. [37] Koordinationspolymere aus Metallionen und organischen Liganden, mittels koordinativer Bindungen gebildet, traten in den frühen 1960er Jahren in Erscheinung, [38] und der Begriff "Koordinationspolymer" wurde 1964 von J. C. Bailar definiert. [39] Koordinationspolymere mit reversiblen koordinativen Bindungen kçnnen auch den supramolekularen Polymeren zugeordnet werden.…”
Section: Geschichte Der Grenzflächenpolymerisationunclassified
Abbildung 1. Chronologie der wichtigsten Entwicklungender Grenzflächenpolymerisation. Der untere (violette) Teil zeigt die wichtigenM eilensteine in der Polymerwissenschaft und der obere Teil die der Grenzflächenpolymerisation.
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