Novel amphiphilic and photo-responsive ABC 3-miktoarm star terpolymers: synthesis, self-assembly and photo-responsive behavior
Novel amphiphilic and photo-responsive ABC 3-miktoarm star terpolymers consisting of hydrophilic poly(ethylene glycol) monomethyl ether (MPEG), hydrophobic polystyrene (PS) and azobenzene-containing poly[6-(4-methoxy-azobenzene-4'-oxy) hexylmethacrylate] (PMMAZO) were synthesized by a combinati...
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Veröffentlicht in: | Polymer chemistry 2013-01, Vol.4 (6), p.1939-1949 |
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Sprache: | eng |
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Zusammenfassung: | Novel amphiphilic and photo-responsive ABC 3-miktoarm star terpolymers consisting of hydrophilic poly(ethylene glycol) monomethyl ether (MPEG), hydrophobic polystyrene (PS) and azobenzene-containing poly[6-(4-methoxy-azobenzene-4'-oxy) hexylmethacrylate] (PMMAZO) were synthesized by a combination of atom transfer radical polymerization (ATRP) and click chemistry. MPEG was first end-capped by an epoxide ring, which was opened by sodium azide for the preparation of the modified MPEG bearing reactive azide group and hydroxyl group (MPEG-(OH)(N sub(3))). Click chemistry was then performed to conjugate alpha -alkynyl- omega -diethylamino-PS and MPEG-(OH)(N sub(3)) for the preparation of a block copolymer with reactive hydroxyl group at the junction point (MPEG(-OH)-b-PS), which was further esterified with 2-bromoisobutyryl bromide to prepare the macroinitiator with reactive bromo group at the central point (MPEG(-Br)-b-PS). Finally, an azobenzene-containing PMMAZO arm was introduced into the diblock copolymer by ATRP of 6-(4-methoxy-azobenzene-4'-oxy) hexylmethacrylate monomer (MMAZO) initiated with macroinitiator MPEG(-Br)-b- PS for the preparation of ABC 3-miktoarm star terpolymer (MPEG)(PS)(PMMAZO). The self-assembled morphologies of the star terpolymers in selective solvents changed from bowl-shaped structures to multibowl-shaped structures with the lengthening of the hydrophobic chains (PS or PMMAZO). Photo-responsive investigation showed that the different aggregation states had a great effect on the photo-induced isomerization behaviors. These results may provide guidelines for the design of effective photoresponsive anisotropic materials. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/c2py21043f |