2020
DOI: 10.1021/acs.macromol.0c00182
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Supramolecular Superparamagnetic Nanocomposites Based on a Magnetite-Filled Unentangled Terpyridine-Functionalized Polymer

Abstract: Le dépôt institutionnel DIAL est destiné au dépôt et à la diffusion de documents scientifiques émanant des membres de l'UCLouvain. Toute utilisation de ce document à des fins lucratives ou commerciales est strictement interdite. L'utilisateur s'engage à respecter les droits d'auteur liés à ce document, principalement le droit à l'intégrité de l'oeuvre et le droit à la paternité.

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Cited by 5 publications
(12 citation statements)
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“…Random copolymerization of n-BA and terpyridine functionalized monomer was performed by reversible addition−fragmentation chain transfer polymerization (RAFT) under bulk conditions at 70 °C using 2-(dodecylthiocarbonothioylthio)-2methylpropionic acid (DDMAT) as RAFT agent following a previously reported procedure. 11 Briefly, AIBN (3 mg, 18.3 μmol), DDMAT (44.5 mg, 0.122 mmol), n-BA (3.37 mL, 23.8 mmol), and acrylate-TPy (535 mg, 1.44 mmol) were introduced into a 10 mL Schlenk tube. After the solution was degassed by six freeze−pump− thaw cycles, the reaction mixture was sealed, purged with argon, and then immersed in a preheated oil bath at 70 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Random copolymerization of n-BA and terpyridine functionalized monomer was performed by reversible addition−fragmentation chain transfer polymerization (RAFT) under bulk conditions at 70 °C using 2-(dodecylthiocarbonothioylthio)-2methylpropionic acid (DDMAT) as RAFT agent following a previously reported procedure. 11 Briefly, AIBN (3 mg, 18.3 μmol), DDMAT (44.5 mg, 0.122 mmol), n-BA (3.37 mL, 23.8 mmol), and acrylate-TPy (535 mg, 1.44 mmol) were introduced into a 10 mL Schlenk tube. After the solution was degassed by six freeze−pump− thaw cycles, the reaction mixture was sealed, purged with argon, and then immersed in a preheated oil bath at 70 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Alternatively, Ramanujan et al developed promising healable rubbers based on copolymers (either polyethylene–vinyl acetate or acrylonitrile butadiene), , but the lack of systematic physical characterization inhibits the adaptation of the concept to more conventional, that is, industry-oriented, chemistries. Alternatively, several research groups attempted to control the solid-to-liquid transition in model supramolecular networks through induction heating. In these examples, ionic aggregates, terpyridine, and ureidopyrimidinone moieties were, respectively, used, without providing strong mechanical properties to the materials, which displayed a shear modulus below 1 MPa or a flow regime at room temperature. Importantly, all the above-mentioned materials (excluding ref ) were prepared through solvent casting, precluding large-scale production.…”
Section: Introductionmentioning
confidence: 99%
“…Alternatively, several research groups attempted to control the solid-to-liquid transition in model supramolecular networks through induction heating. In these examples, ionic aggregates, terpyridine, and ureidopyrimidinone moieties were, respectively, used, without providing strong mechanical properties to the materials, which displayed a shear modulus below 1 MPa or a flow regime at room temperature. Importantly, all the above-mentioned materials (excluding ref ) were prepared through solvent casting, precluding large-scale production. In summary, although magneto-responsive thermoplastic rubbers are henceforth quite popular to serve as actuators, it appears that triggering their phase transition in view of a possible healing or post-processing treatment remains a largely uncharted territory, limited to the field of adhesives , and bioengineering-oriented hydrogels .…”
Section: Introductionmentioning
confidence: 99%
“…[19][20][21][22] Surface ligands that interact with the polymer matrix through hydrogen bonding or other attractive interactions can serve as transient physical crosslinks that increase the overall modulus of the composite structure. [23][24][25][26][27] The long-range order of microphase separated BCPs dominates the viscoelasticity and rheological properties at long time scales. 28 Specifically in BBCPs, the dense grafting of side chains suppresses chain entanglements in the melt state, resulting in highly mobile "liquid-like" rheology.…”
Section: Introductionmentioning
confidence: 99%
“…NPs are also much stiffer than the polymer matrix and can enhance the mechanical properties through structural percolation or topological constraints on the polymer chains 19–22 . Surface ligands that interact with the polymer matrix through hydrogen bonding or other attractive interactions can serve as transient physical crosslinks that increase the overall modulus of the composite structure 23–27 …”
Section: Introductionmentioning
confidence: 99%