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Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
Enlarging the Toolbox: Epoxide Termination of Polyferrocenylsilane (PFS) as a Key Step for the Synthesis of
Adrian Natalello1,2, Arda Alkan1,3, Andreas Friedel1
1Institute of Organic Chemistry, Johannes Gutenberg-University (JGU), Duesbergweg 10-14, 55099 Mainz, Germany.
Abstract:
Epoxide termination and functionalization of living poly(ferrocenyldimethylsilane) (PFDMS) is introduced by precapping the living PFDMS with a 4/2 molar mixture of 1,1-diphenylethylene and 1,1-dimethylsilacyclobutane acting as a "carbanion pump" system. Subsequent addition of allyl glycidyl ether (AGE) leads to quantitatively functionalized PFDMS-AGE polymers with molecular weights between 1500 and 15 400 g mol-1 and polydispersity indices ≤1.10, carrying one hydroxyl group and an additional allylic double bond. PFDMS-AGE was then applied as a macroinitiator for the living anionic ring-opening polymerization of ethylene oxide (EO) to generate amphiphilic and water-soluble poly(ferrocenyldimethylsilane-b-ethylene oxide) block copolymers with a low polydispersity index. All polymers have been characterized by 1H NMR spectroscopy, DOSY 1H NMR spectroscopy, size exclusion chromatography (SEC), and MALDI-ToF mass spectrometry. In addition, for the characterization of the morphology of the PFDMS-b-PEO block copolymers transmission electron microscopy (TEM) was performed in methanol, confirming the formation of cylindrical micelles with an organometallic core and polyether corona.
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