| People | Locations | Statistics |
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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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Dubois, Philippe
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (24/24 displayed)
- 2011Novel polyesteramide-based di- and triblock copolymerscitations
- 2008Controlled synthesis of amphiphilic block copolymers based on polyester and poly(amino methacrylate)citations
- 2008Designing polylactide/clay nanocomposites for textile applicationscitations
- 2008Undecyltin trichloride grafted onto cross-linked polystyrenecitations
- 2008CH-π interactions as the driving force for silicone-based nanocomposites with exceptional propertiescitations
- 2007(Plasticized) Polylactide/clay nanocomposite textilecitations
- 2007Polylactide compositions. Part 1citations
- 2007Copolymerization of vinyl acetate with 1-octene and ethylene by cobalt-mediated radical polymerizationcitations
- 2006Copper-based supported catalysts for the atom transfer radical polymerization of methyl methacrylatecitations
- 2005Polylactide/montmorillonite nanocompositescitations
- 2005(Plasticized) polylactide/(organo-)clay nanocomposites by in situ intercalative polymerizationcitations
- 2005Nickel-catalyzed supported ATRP of methyl methacrylate using cross-linked polystyrene triphenylphosphine as ligandcitations
- 2004End-grained wood-polyurethane composites, 1 synthesis, morphology and characterizationcitations
- 2004Synthesis of melt-stable and semi-crystalline poly(1,4-dioxan-2-one) by ring-opening (co)polymerisation of 1,4-dioxan-2-one with different lactonescitations
- 2004Supported nickel bromide catalyst for Atom Transfer Radical Polymerization (ATRP) of methyl methacrylatecitations
- 2004Diblock copolymers based on 1,4-dioxan-2-one and ε-caprolactonecitations
- 2003Intercalative polymerization of cyclic esters in layered silicatescitations
- 2003Biodegradation of poly(ε-caprolactone)/starch blends and composites in composting and culture environmentscitations
- 2003Exfoliated polylactide/clay nanocomposites by in-situ coordination-insertion polymerizationcitations
- 2002New nanocomposite materials based on plasticized poly(L-lactide) and organo-modified montmorillonitescitations
- 2001Poly(ϵ-caprolactone) layered silicate nanocompositescitations
- 2001Some thermodynamic, kinetic, and mechanistic aspects of the ring-opening polymerization of 1,4-dioxan-2-one initiated by Al(OiPr)3 in bulkcitations
- 2001Mechanisms and kinetics of thermal degradation of poly(ε-caprolactone)citations
- 2000New developments on the ring opening polymerisation of polylactidecitations
Places of action
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article
Controlled synthesis of amphiphilic block copolymers based on polyester and poly(amino methacrylate)
Abstract
<p>The synthesis of amphiphilic and adaptative block copolymers has been envisioned following a commutative two-step strategy involving atom transfer radical polymerization (ATRP) and the Huisgen-1,3-dipolar cycloaddition techniques. The reliability of this strategy is based on the use of an azido-containing ATRP initiator, the 2-(2-azidoethoxy)ethylbromoisobutyrate (N<sub>3</sub>E<sup>i</sup>BBr), able to be "clicked" to an alkyne-terminated derivative and to promote the ATRP polymerization from the active site. In the context of this work, an alkyne-terminated poly(ε-caprolactone) produced by ring-opening polymerization (ROP) of CL was employed as hydrophobic "clickable" segment. The N<sub>3</sub>E<sup>i</sup>BBr initiator was obtained by nucleophilic substitution of the chloride atom from 2-(2-chloroethoxy)ethanol by an azide function and followed by the esterification of the hydroxy function by bromoisobutyryl bromide. This initiator was employed in polymerization of N,N-dimethylamino-2-ethyl methacrylate (DMAEMA) monomer by ATRP in THF at 60 °C using CuBr complexed by 1,1,4,7,10,10-hexamethyltriethylenetetramine (HMTETA) as catalytic complex. Low initiation efficiencies were obtained and they were ascribed to intramolecular cyclization during the polymerization as evidenced by ESI-MS and 2D NMR spectroscopy. The "Click" coupling reaction was performed in THF at r.t. and was found to be efficient when using CuBr complexed by 2,2′-bipyridine ligand. To circumvent the low initiation efficiency, the N<sub>3</sub>E<sup>i</sup>BBr could be "clicked" in a first step to PCL precursors before initiating the polymerization of DMAEMA monomer by ATRP. In this context, various catalytic complexes in different composition ratio were employed to optimize the "click" coupling step. Moreover, this strategy was found to be suitable to produce well-defined PCL-b-PDMAEMA block copolymers, characterized by narrow polydispersity indices. Since ATRP and the Huisgen-1,3-dipolar cycloaddition both require the use of a copper(I)-based catalyst, the two first strategies were merged in a "one-pot" process in order to obtain in one step a well-defined block copolymer characterized by a narrow polydispersity index and predictable composition and block lengths.</p>