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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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Hao, X.
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Publications (6/6 displayed)
- 2016Giant spin-torque diode sensitivity at low input power in theabsence of bias magnetic fieldcitations
- 2010Monitoring microstructure changes in rod online by using induction spectroscopycitations
- 2004Molecular composite materials formed from block copolymers containing a side-chain liquid crystalline segment and an amorphous styrene/maleic anhydride segmentcitations
- 2004Reversible addition fragmentation chain transfer polymerization of sterically hindered monomers: Toward well-defined rod/coil architecturescitations
- 2004Dendrimers as scaffolds for multifunctional reversible addition-fragmentation chain transfer agents: Syntheses and polymerizationcitations
- 2003A New Chemo-Enzymatic Route to Side-Chain Liquid-Crystalline Polymers: The Synthesis and Polymerization of 6-(4-Methoxybiphenyl-4′-oxy)hexyl Vinyl Hexanedioatecitations
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article
Molecular composite materials formed from block copolymers containing a side-chain liquid crystalline segment and an amorphous styrene/maleic anhydride segment
Abstract
Side-chain liquid crystalline block polymers containing a poly[6-[4-(4′-methoxyphenyl)phenoxy]hexyl methacrylate] (PMMA-LC) segment and a styrene-co-maleic anhydride segment (alternating structure) were prepared via reversible addition fragmentation chain transfer (RAFT) polymerization. PMMA-LC was initially prepared via RAFT polymerization mediated by 2-(2-cyanopropyl)dithiobenzoate (CPDB). The resulting polymer was subsequently isolated and used to re-initiate styrene/maleic anhydride alternating copolymerization. The block copolymerization proceeded to intermediate conversions with narrow polydispersities, however at higher conversions some molecular weight broadening was observed and this was attributed to radical-radical termination reactions. The resulting polymers were analyzed via size exclusion chromatography (SEC), differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). Microporous honeycomb structured films were cast from solutions of the block copolymers to form porous molecular composites. © 2004 Elsevier Ltd. All rights reserved.