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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Frey, Holger
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (29/29 displayed)
- 2024Supersoft Polymer Melts in Binary Blends of Bottlebrush cis‐1,4‐Polyfarnesene and cis‐1,4‐Polyisoprenecitations
- 2023Merging styrene and diene structures to a cyclic diene : anionic polymerization of 1-vinylcyclohexene (VCH)
- 2023Merging Styrene and Diene Structures to a Cyclic Diene: Anionic Polymerization of 1‐Vinylcyclohexene (VCH)citations
- 2023Bifunctional Carbanionic Synthesis of Fully Bio-Based Triblock Structures Derived from β-Farnesene and ll-Dilactide: Thermoplastic Elastomerscitations
- 2023Bifunctional Carbanionic Synthesis of Fully Bio-Based Triblock Structures Derived from β-Farnesene and ll-Dilactide: Thermoplastic Elastomers
- 2023Revealing the monomer gradient of polyether copolymers prepared using N‐heterocyclic olefins : metal‐free anionic versus zwitterionic Lewis pair polymerization
- 2023Bifunctional carbanionic synthesis of fully bio-based triblock structures derived from β-farnesene and LL-dilactide : thermoplastic elastomers
- 2022Glycidyl cinnamate : copolymerization with glycidyl ethers, in-situ NMR kinetics, and photocrosslinking
- 2022In situ kinetics reveal the influence of solvents and monomer structure on the anionic ring-opening copolymerization of epoxides
- 2020Efficiency Boosting of Surfactants with Poly(ethylene oxide)-Poly(alkyl glycidyl ether)s: A New Class of Amphiphilic Polymerscitations
- 2020Tapered copolymers of styrene and 4-vinylbenzocyclobutene via carbanionic polymerization for crosslinkable polymer films
- 2020Synthesis and Solution Processing of Nylon-5 Ferroelectric Thin Filmscitations
- 2020Synthesis and solution processing of nylon-5 ferroelectric thin films : the renaissance of odd-nylons?
- 2019Glycidyl tosylate: polymerization of a “non-polymerizable” monomer permits universal post-functionalization of polyethers
- 2019Solution-processed transparent ferroelectric nylon thin filmscitations
- 2017Acid-labile surfactants based on poly(ethyleneglycol), carbon dioxide and propylene oxidecitations
- 2016Oxidation-responsive and "clickable" poly(ethylene glycol) via copolymerization of 2-(methylthio)ethyl glycidyl ethercitations
- 2016Acid-Labile Amphiphilic PEO-b-PPO-b-PEO Copolymerscitations
- 2016Hierachical Ni@Fe2O3 superparticles through epitaxial growth of gamma-Fe2O3 nanorods on in situ formed Ni nanoplatescitations
- 2016Processing and adjusting the hydrophilicity of poly(oxymethylene) (co)polymerscitations
- 2014Stimuli-Responsive Tertiary Amine Functional PEGs Based on N,N-Dialkylglycidylaminescitations
- 2014Ferrocene-containing multifunctional polyetherscitations
- 2013Enlarging the toolboxcitations
- 2013Ferrocenyl glycidyl ethercitations
- 2011Rapid access to polyfunctional lipids with complex architecture via oxyanionic ring-opening polymerizationcitations
- 2011PEG-based multifunctional polyethers with highly reactive vinyl-ether side chains for click-type functionalizationcitations
- 2010"Functional poly(ethylene glycol)"citations
- 2008Carbanions on tap - Living anionic polymerization in a microstructured reactorcitations
- 2008Ionic polymerizations in microstructured reactors
Places of action
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article
Acid-labile surfactants based on poly(ethyleneglycol), carbon dioxide and propylene oxide
Abstract
<p>Partially degradable, nonionic AB and ABA type di- and triblock copolymers based on poly(propylene carbonate) and poly(ethylene glycol) blocks were synthesized via immortal copolymerization of carbon dioxide and propylene oxide, using mPEG or PEG as a macroinitiator, and (R,R)-(salcy)-CoOBzF<sub>5</sub> as a catalyst in a solvent-free one-pot procedure. The amphiphilic surfactants were prepared with molecular weights (M<sub>n</sub>) between 2800 and 10,000 g mol<sup>-1</sup> with narrow molecular weight distributions (1.03-1.09). The copolymers were characterized using <sup>1</sup>H-, <sup>13</sup>C- and DOSY-NMR spectroscopy and size exclusion chromatography (SEC). Surface-active properties were determined by surface tension measurements (critical micelle concentration, CMC; CMC range: 1-14 mg mL<sup>-1</sup>). Degradation of the acid-labile polycarbonate blocks was investigated in aqueous solution using online <sup>1</sup>H-NMR spectroscopy and SEC. The amphiphilic polymers were used as surfactants in a direct miniemulsion polymerization for poly(styrene) (PS) nanoparticles with mean diameter of 270 to 940 nm. The usage of an acid-triggered precipitation of the emulsion simplified the separation of the particles from the surfactant and purification of the nanoparticles.</p>