Ruettiger, Christian ; Appold, Michael ; Didzoleit, Haiko ; Eils, Adjana ; Dietz, Christian ; Stark, Robert W. ; Stühn, B. ; Gallei, Markus (2016)
Structure Formation of Metallopolymer-Grafted Block Copolymers.
In: Macromolecules, 49 (9)
Article, Bibliographie
Abstract
Microphase separation drives the structure formation in block copolymers. Here, functional metallopolymer-grafted diblock copolymers consisting of polystyrene-block-polyisoprene (PS-b-PI) as polymer backbone featuring low molar mass polyferrocenyldimethylsilane (PFS) and polyvinylferrocene (PVFc) are synthesized via an iterative anionic grafting-to polymerization strategy. PS-b-PI block copolymers having about 30 mol % 1,2-polyisoprene moieties are subjected to platinum-catalyzed hydrosilylation reaction for the introductiorr of chlorosilane groups. The Si Cl moieties are shown to efficiently react with the active metallopolymers yielding :block-selective metallopolymer-grafted copolymers with 34 vol % PVFc and 43 vol % PFS as evidenced by H-1 NMR spectroscopy as well as size exclusion chromatography. The microphase separation of the functional metallopolyiner-grafted block copolymers is evidenced via TEM measurements revealing fascinating morphologies. The structure formation of the PVFc-grafted block copolymers is, studied in more detail by small-angle X-ray scattering, wide-angle X-ray scattering, and atomic force microscopy measurements evidencing a lamellar, morphology featuring a spherical substructure for the PVFc segments, inside the polyisoprene lamellae.
Item Type: | Article |
---|---|
Erschienen: | 2016 |
Creators: | Ruettiger, Christian ; Appold, Michael ; Didzoleit, Haiko ; Eils, Adjana ; Dietz, Christian ; Stark, Robert W. ; Stühn, B. ; Gallei, Markus |
Type of entry: | Bibliographie |
Title: | Structure Formation of Metallopolymer-Grafted Block Copolymers |
Language: | English |
Date: | 26 April 2016 |
Journal or Publication Title: | Macromolecules |
Volume of the journal: | 49 |
Issue Number: | 9 |
URL / URN: | http://dx.doi.org/10.1021/acs.macromol.6b00577 |
Abstract: | Microphase separation drives the structure formation in block copolymers. Here, functional metallopolymer-grafted diblock copolymers consisting of polystyrene-block-polyisoprene (PS-b-PI) as polymer backbone featuring low molar mass polyferrocenyldimethylsilane (PFS) and polyvinylferrocene (PVFc) are synthesized via an iterative anionic grafting-to polymerization strategy. PS-b-PI block copolymers having about 30 mol % 1,2-polyisoprene moieties are subjected to platinum-catalyzed hydrosilylation reaction for the introductiorr of chlorosilane groups. The Si Cl moieties are shown to efficiently react with the active metallopolymers yielding :block-selective metallopolymer-grafted copolymers with 34 vol % PVFc and 43 vol % PFS as evidenced by H-1 NMR spectroscopy as well as size exclusion chromatography. The microphase separation of the functional metallopolyiner-grafted block copolymers is evidenced via TEM measurements revealing fascinating morphologies. The structure formation of the PVFc-grafted block copolymers is, studied in more detail by small-angle X-ray scattering, wide-angle X-ray scattering, and atomic force microscopy measurements evidencing a lamellar, morphology featuring a spherical substructure for the PVFc segments, inside the polyisoprene lamellae. |
Divisions: | 11 Department of Materials and Earth Sciences 11 Department of Materials and Earth Sciences > Material Science 11 Department of Materials and Earth Sciences > Material Science > Physics of Surfaces Exzellenzinitiative Exzellenzinitiative > Clusters of Excellence 05 Department of Physics 05 Department of Physics > Institute for condensed matter physics (2021 merged in Institute for Condensed Matter Physics) 05 Department of Physics > Institute for condensed matter physics (2021 merged in Institute for Condensed Matter Physics) > Experimental Condensed Matter Physics Zentrale Einrichtungen |
Date Deposited: | 08 Jun 2016 12:20 |
Last Modified: | 29 Jan 2019 08:56 |
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