Nature Communications · 2019 · 61 citations · 46 references
Natural SciencesChemical EngineeringChemistryPolymer ChemistryPolymer EngineeringPolymer MaterialsHydrogelsPolymer FunctionalizationPolymer StructurePolymer SynthesisPolymerization ChemistryPolymerization ProcessesCopolymer Composition DistributionCopolymerizationCopolymerization BehaviorCopolymerization StrategiesFunctionalizationPolymer Chain StatisticsPolymer TherapeuticsReversible-deactivation Radical Polymerization
Even though functional copolymers with a low percentage of functional comonomer units (up to 20 mol%) are widely used, for instance for the development of polymer therapeutics and hydrogels, insights in the functional group distribution over the actual chains are lacking and the average composition is conventionally used to describe the functionalization degree. Here we report the visualization of the monomer distribution over the different polymer chains by a synergetic combination of experimental and theoretical analysis aiming at the construction of functionality-chain length distributions (FUNC-CLDs). A successful design of the chemical structure of the comonomer pair, the initial functional comonomer amount (13 mol%), and the temperature (100 °C) is performed to tune the FUNC-CLD of copoly(2-oxazoline)s toward high functionalization degree for both low (100) and high (400) target degrees of polymerization. The proposed research strategy is generic and extendable to a broad range of copolymerization chemistries, including reversible deactivation radical polymerization.
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Keigo Aoi · Progress in Polymer Science · 1996 · 396 citations
Polymerization-induced thermal self-assembly (PITSA)
C. Adrian Figg, Alexandre Simula, Kalkidan A. Gebre et al. · Chemical Science · 2014 · 328 citations · Full text
Natural Sciences, Materials Engineering, Materials Science +16
The chemistry of poly(2-oxazoline)s
Bart Verbraeken, Bryn D. Monnery, Kathleen Lava et al. · European Polymer Journal · 2016 · 281 citations