Functionalization of Titanium Surfaces ...
Document type :
Article dans une revue scientifique: Article original
DOI :
Permalink :
Title :
Functionalization of Titanium Surfaces with Polymer Brushes Prepared from a Biomimetic RAFT Agent
Author(s) :
Zobrist, Cedric [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Sobocinski, Jonathan [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Lyskawa, Joel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Fournier, David [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Gaucher, Valerie [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Traisnel, Michel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Jimenez, Maude [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Unité Matériaux et Transformations (UMET) - UMR 8207
Sobocinski, Jonathan [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Lyskawa, Joel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Fournier, David [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Gaucher, Valerie [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Traisnel, Michel [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Jimenez, Maude [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Woisel, Patrice [Auteur]
Unité Matériaux et Transformations (UMET) - UMR 8207
Journal title :
Macromolecules
Volume number :
44
Pages :
5883-5892
Publisher :
American Chemical Society (ACS)
Publication date :
2011-08-09
ISSN :
5883–5892
English keyword(s) :
RAFT polymerization
Aromatic compounds
Titanium
Amines
Polymers
Aromatic compounds
Titanium
Amines
Polymers
HAL domain(s) :
Chimie/Matériaux
Chimie/Polymères
Chimie/Polymères
English abstract : [en]
Well-defined dopamine end-functionalized polymers were synthesized by employing the reversible addition–fragmentation chain transfer (RAFT) polymerization technique. tert-Butyl acrylate, N-isopropylacrylamide, and styrene ...
Show more >Well-defined dopamine end-functionalized polymers were synthesized by employing the reversible addition–fragmentation chain transfer (RAFT) polymerization technique. tert-Butyl acrylate, N-isopropylacrylamide, and styrene monomers were polymerized in the presence of azobis (isobutyronitrile) and a new catechol-based biomimetic RAFT agent incorporating a trithiocarbonate unit. All RAFT polymerizations exhibited pseudofirst-order kinetics, a linear increase of the number-average molar mass (Mn SEC) with conversion and narrow molar mass distributions (polydispersity <1.2). The resulting homopolymers exhibited the electroactive catechol and the ω-trithiocarbonyl end groups. Subsequent immobilization of dopamine end-functionalized polymers on titanium surfaces was monitored by using a surface plasmon resonance (SPR) sensor, and the resulting films were characterized by contact angle, infrared ATR spectroscopy, atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS).Show less >
Show more >Well-defined dopamine end-functionalized polymers were synthesized by employing the reversible addition–fragmentation chain transfer (RAFT) polymerization technique. tert-Butyl acrylate, N-isopropylacrylamide, and styrene monomers were polymerized in the presence of azobis (isobutyronitrile) and a new catechol-based biomimetic RAFT agent incorporating a trithiocarbonate unit. All RAFT polymerizations exhibited pseudofirst-order kinetics, a linear increase of the number-average molar mass (Mn SEC) with conversion and narrow molar mass distributions (polydispersity <1.2). The resulting homopolymers exhibited the electroactive catechol and the ω-trithiocarbonyl end groups. Subsequent immobilization of dopamine end-functionalized polymers on titanium surfaces was monitored by using a surface plasmon resonance (SPR) sensor, and the resulting films were characterized by contact angle, infrared ATR spectroscopy, atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS).Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
INRA
ENSCL
CNRS
INRA
ENSCL
Collections :
Research team(s) :
Ingénierie des Systèmes Polymères
Submission date :
2021-07-16T11:35:47Z
2021-08-26T12:18:57Z
2021-08-26T12:18:57Z