Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Sylvie Boileau"'
Publikováno v:
Polymer International. 66:1389-1394
Supramolecular assemblies based on 4,4’-bipyridine as H-acceptor and a terthiophene carboxylic acid (3-TTAA) as H-donor were synthesized and characterized by FTIR and DSC. Their electropolymerization was successful in methylene chloride or in aceto
Autor:
Sylvie Boileau, Alina V. Maryasevskaya, Denis V. Anokhin, Deogratias Urayeneza, Dimitri A. Ivanov, Blandine Brissault, Laurent Michely, Jacques Penelle, Nicolas Illy, Egor A. Bersenev
Publikováno v:
Macromolecules
Macromolecules, 2019, 52 (23), pp.9199-9207. ⟨10.1021/acs.macromol.9b01559⟩
Macromolecules, American Chemical Society, 2019, 52 (23), pp.9199-9207. ⟨10.1021/acs.macromol.9b01559⟩
Macromolecules, 2019, 52 (23), pp.9199-9207. ⟨10.1021/acs.macromol.9b01559⟩
Macromolecules, American Chemical Society, 2019, 52 (23), pp.9199-9207. ⟨10.1021/acs.macromol.9b01559⟩
International audience; The synthesis and structural characterization of linear PolyC3 polymers containing trimethylene-1,1-dicarboxylate structural repeat units with C6F13 and C8F17 fluorinated side chains is described for the first time, and their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c365f25b17a44fd97ebee673f93a85b3
https://hal.science/hal-02370804
https://hal.science/hal-02370804
Autor:
Hervé Bouaziz, Nathalie Thilly, Anaïs Roche Interne e année du Des d’anesthésie-réanimation, Sylvie Boileau
Publikováno v:
Canadian Journal of Anesthesia/Journal canadien d'anesthésie. 65:597-599
Autor:
D.L. Versace, Christine Gaillet, Cédric Lorenzini, Cédric Lorthioir, Estelle Renard, Sylvie Boileau, Valérie Langlois
Publikováno v:
Polymer. 55:4432-4440
New bridged silsesquioxanes derived from isosorbide were synthesized, according to the sol–gel process, by acidic or basic hydrolysis and condensation of a bis-trimethoxysilyl precursor. The latter was prepared by thiol-ene photoaddition of 3-(trim
Autor:
Sylvie Boileau, Nicolas Illy
Publikováno v:
Progress in Polymer Science. 36:1132-1151
Recently, nitrogen–phosphorous hybrid organobases such as phosphazene bases (PBs), which possess a remarkably high basicity, have been extensively studied in organic synthesis. Their applications in the domain of anionic polymerization are reviewed
Publikováno v:
Macromolecules
Macromolecules, American Chemical Society, 2010, 43 (21), pp.8782-8789. ⟨10.1021/ma1016506⟩
Macromolecules, 2010, 43 (21), pp.8782-8789. ⟨10.1021/ma1016506⟩
Macromolecules, American Chemical Society, 2010, 43 (21), pp.8782-8789. ⟨10.1021/ma1016506⟩
Macromolecules, 2010, 43 (21), pp.8782-8789. ⟨10.1021/ma1016506⟩
International audience; A synthetic method involving the in situ generation of an anionic initiator X− obtained by reaction of its conjugate acid precursor XH with ButP4 phosphazene base was tested as a possible way to easily and better control the
Publikováno v:
Macromolecular Chemistry and Physics
Macromolecular Chemistry and Physics, Wiley-VCH Verlag, 2018, 219 (1), pp.1700463. ⟨10.1002/macp.201700463⟩
Macromolecular Chemistry and Physics, Wiley-VCH Verlag, 2018, 219 (1), pp.1700463. ⟨10.1002/macp.201700463⟩
International audience
Publikováno v:
Macromolecular Rapid Communications. 30:1731-1735
The successful activation observed when using ButP4 phosphazene base and thiophenol or bisthiols for the anionic ring opening polymerization (ROP) of di-n-propyl cyclopropane-1,1- dicarboxylate is described. Well-defined monofunctional or difunctiona
Publikováno v:
Express Polymer Letters. 3:446-451
A series of novel oligomers with promesogenic groups on both termini were prepared by a hydrosilylation reac- tion between well-defined telechelic oligocarbosilazanes end-fitted with vinylsilane (SiVi) groups and promesogenic com- pounds containing o
Publikováno v:
Polymer. 48:687-695
Combinations of fluorinated and silicone based elastomers were elaborated through the in situ synthesis of interpenetrating polymer networks (IPNs). The PDMS network was formed by dibutyltindilaurate catalyzed addition between the hydroxy end groups