Preparation of a xanthate-terminated dextran by click chemistry:: Application to the synthesis of polysaccharide-coated nanopartides via surfactant-free ab initio emulsion polymerization of vinyl acetate
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作者:
Bernard, Julien
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Univ Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, France
Univ INSA Lyon, CNRS, UMR 5623, LMM, F-69621 Villeurbanne, FranceUniv Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, France
Bernard, Julien
[1
,2
]
Save, Maud
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Univ Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, FranceUniv Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, France
Save, Maud
[1
]
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Arathoon, Benoit
[1
]
Charleux, Bernadette
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Univ Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, FranceUniv Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, France
Charleux, Bernadette
[1
]
机构:
[1] Univ Paris 06, CNRS, UMR 7610, Lab Chim Polymeres, F-75252 Paris 05, France
[2] Univ INSA Lyon, CNRS, UMR 5623, LMM, F-69621 Villeurbanne, France
Stable monodisperse poly(vinyl acetate) (PVAc) submicronic latex particles were synthesized by ab initio batch emulsion polymerization using a dextran derivative from renewable resource as an efficient steric stabilizer. The dextran end-functionalized by a xanthate moiety was synthesized by Huisgen's 1,3-dipolar cycloaddition (click chemistry). It was applied as a macromolecular RAFT (reversible addition fragmentation chain transfer) agent in surfactant-free emulsion polymerization of vinyl acetate to form in situ an amphiphilic block copolymer able to efficiently stabilize the latex particles. The method afforded the preparation of high solids content (27%) latices coated by dextran. Both the kinetic study and the molar mass analyses confirmed the involvement of the dithiocarbonate group in the emulsion polymerization process. (c) 2008 Wiley Periodicals, Inc.
机构:
Univ Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, France
Labarre, D
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Couvreur, P
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Vauthier, C
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Univ Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, France
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, France
Labarre, D
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Couvreur, P
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Vauthier, C
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Univ Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, France
机构:
Univ Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, France
Labarre, D
;
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机构:
Couvreur, P
;
Vauthier, C
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h-index: 0
机构:
Univ Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, UMR 8612, CNRS, F-92296 Chatenay Malabry, France
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, France
Labarre, D
;
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机构:
Couvreur, P
;
Vauthier, C
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, FranceUniv Paris 11, Fac Pharm, CNRS, UMR 8612,Lab Phys Chim Pharmacotech & Biopharm, F-92296 Chatenay Malabry, France