0000000000451355
AUTHOR
Jan Morsbach
showing 6 related works from this author
Die lebende anionische Polymerisation
2017
Zusammenfassung Vor sechzig Jahren entdeckte Michael Szwarc die lebende anionische Polymerisation. Trotz ihrer hohen synthetischen Anforderungen ist sie bis heute die praziseste Methode zur Herstellung von wohldefinierten Polymeren und inspirierte zahlreiche neue Polymerisationsmethoden. Masgeschneiderte Blockcopolymere finden sich in den verschiedensten Anwendungen von High-End-Verpackungsmaterialien uber die Elektronik bis hin zu Nanomedizin.
Redox-Responsive Block Copolymers: Poly(vinylferrocene)-b-poly(lactide) Diblock and Miktoarm Star Polymers and Their Behavior in Solution
2013
The synthesis of diblock and miktoarm star polymers containing poly(vinylferrocene) (PVFc) and poly(l-lactide) (PLA) blocks is introduced. End functionalization of PVFc was carried out via end capping of living carbanionic PVFc chains with benzyl glycidyl ether (BGE). By hydrogenolysis of the benzyl protecting group a dihydroxyl end-functionalized PVFc was obtained. Both monohydroxyl- and dihydroxyl-functionalized PVFcs have been utilized as macroinitiators for the subsequent polymerization of l-lactide via catalytic ring-opening polymerization. A series of block copolymers and AB2 miktoarm star polymers was synthesized with varied PLA chain lengths. All polymers were characterized in detai…
Vinylphenylglycidyl ether-based colloidal architectures: high-functionality crosslinking reagents, hybrid raspberry-type particles and smart hydropho…
2014
An efficient synthetic strategy for the preparation of monodisperse colloidal core/shell architectures with reactive epoxy functionalities is reported, based on the bifunctional vinylphenylglycidyl ether monomer. Accessibility of the reactive immobilized epoxy moieties was quantified by UV/vis spectroscopy in an isorefractive medium. Inorganic–organic hybrid raspberry-type architectures revealed a tremendous inpact on the surface wettability of water.
Living Polymer Chains with Predictable Molecular Weight and Dispersity via Carbanionic Polymerization in Continuous Flow: Mixing Rate as a Key Parame…
2016
Aiming at systematic variation of the parameter dispersity, Đ (or “polydispersity”), living polymers with predictable dispersity (Đ = 1.15–2.20) and controlled molecular weights (Mn = 3200–18 500 g mol–1) were prepared via carbanionic polymerization. The approach relies on a continuous flow reactor equipped with a tangential four-way jet micromixing device. By varying the total flow rate, the mixing efficiency of the initiator (sec-BuLi) and the corresponding vinyl monomers is controlled, resulting in polymers with predefined dispersity, while the number-average molecular weight, Mn, is kept constant. In this manner living polystyrene (PS), poly(p-methylstyrene) (PpMeS), and poly(2-vinylpyr…
Polyvinylferrocene-Based Amphiphilic Block Copolymers Featuring Functional Junction Points for Cross-Linked Micelles
2016
The synthesis of high-molecular-weight, well-defined poly(vinylferrocene)-block-poly(ethylene glycol) (PVFc-b-PEG) diblock copolymers (Mn = 13 000–44 000 g mol–1; Đ = 1.29–1.34) with precisely one allyl group at the junction point is introduced. Allyl glycidyl ether (AGE) was used to end-functionalize PVFc, resulting in hydroxyl functional macroinitiators for the oxyanionic polymerization of ethylene oxide. The self-assembly behavior of the amphiphilic PVFc-b-PEG copolymers in water has been investigated in a detailed manner, using dynamic light scattering (DLS) and transmission electron microscopy (TEM). The redox activity of the PVFc block was confirmed by UV/vis spectroscopy, while cyclo…
Living Anionic Polymerization in Continuous Flow: Facilitated Synthesis of High-Molecular Weight Poly(2-vinylpyridine) and Polystyrene
2014
We describe the living anionic polymerization of 2-vinylpyridine (2VP) and styrene (S) in continuous flow, comparing two micromixing devices with different mixing principles. The use of a continuous flow setup reduces the experimental effort for living anionic polymerizations significantly, compared to a conventional batch system. By adjusting the ratio of the flow rates of the monomer and initiator solutions a variety of different molecular weights can be rapidly synthesized within several minutes, using one setup. Additionally, a comparison of the influence of the two different mixing devices—an interdigital micromixer (SIMM-V2) leading to laminar mixing and a tangential four-way jet mixi…