Synthesis, post-modification and self-assembled thin films of pentafluorostyrene containing block copolymers

被引:28
作者
Riedel, Maria [1 ]
Stadermann, Jan [1 ]
Komber, Hartmut [1 ]
Simon, Frank [1 ]
Voit, Brigitte [1 ]
机构
[1] Leibniz Inst Polymer Res Dresden eV, D-01069 Dresden, Germany
关键词
Block copolymers; Click reactions; Pentafluorostyrene; RAFT; Self-assembly behaviour; Thin films; FUNCTIONAL POLYMERS; CLICK; CYCLOADDITIONS; PHASE;
D O I
10.1016/j.eurpolymj.2010.10.010
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Block copolymers consisting of a pentafluorostyrene (PFS) block and a hydrophilic block were synthesized by RAFT polymerisation. The hydrophilic blocks consist of methacrylate derivatives, 4-hydroxystyrene or 4-vinylpyridine monomers. The block copolymers were obtained with narrow molecular weight distributions and the molecular weights were in good agreement with the theoretical values. In addition, a model thiol was reacted with the PFS moieties of the block copolymers. This polymer-analogous reaction was performed under ambient conditions in high yields resulting quantitatively in para-substitution of the pentafluorophenyl rings. Finally, thin films consisting of block copolymers that showed strong phase-segregation behaviour and ordered nanostructured surfaces consisting of both blocks were obtained. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:675 / 684
页数:10
相关论文
共 28 条
[1]   Clicking Pentafluorostyrene Copolymers: Synthesis, Nanoprecipitation, and Glycosylation [J].
Becer, C. Remzi ;
Babiuch, Krzysztof ;
Pilz, David ;
Hornig, Stephanie ;
Heinze, Thomas ;
Gottschaldt, Michael ;
Schubert, Ulrich S. .
MACROMOLECULES, 2009, 42 (07) :2387-2394
[2]   Searching for more effective agents and conditions for the RAFT polymerization of MMA: Influence of dithioester substituents, solvent, and temperature [J].
Benaglia, M ;
Rizzardo, E ;
Alberti, A ;
Guerra, M .
MACROMOLECULES, 2005, 38 (08) :3129-3140
[3]   CuI-catalyzed alkyne-azide "click" cycloadditions from a mechanistic and synthetic perspective [J].
Bock, VD ;
Hiemstra, H ;
van Maarseveen, JH .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 2006 (01) :51-68
[4]   Additive-driven phase-selective chemistry in block copolymer thin films: The convergence of top-down and bottom-up approaches [J].
Du, P ;
Li, MQ ;
Douki, K ;
Li, XF ;
Garcia, CRW ;
Jain, A ;
Smilgies, DM ;
Fetters, LJ ;
Gruner, SM ;
Wiesner, U ;
Ober, CK .
ADVANCED MATERIALS, 2004, 16 (12) :953-+
[5]   Block copolymer thin films: Physics and applications [J].
Fasolka, MJ ;
Mayes, AM .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :323-355
[6]   Diblock copolymers as scaffolds for efficient functionalization via click chemistry [J].
Fleischmann, Sven ;
Komber, Hartmut ;
Voit, Brigitte .
MACROMOLECULES, 2008, 41 (14) :5255-5264
[7]   Modification of polymer surfaces by click chemistry [J].
Fleischmann, Sven ;
Hinrichs, Karsten ;
Oertel, Ulrich ;
Reichelt, Senta ;
Eichhorn, Klaus-Jochen ;
Voit, Brigitte .
MACROMOLECULAR RAPID COMMUNICATIONS, 2008, 29 (12-13) :1177-1185
[8]   New polymer synthesis by nitroxide mediated living radical polymerizations [J].
Hawker, CJ ;
Bosman, AW ;
Harth, E .
CHEMICAL REVIEWS, 2001, 101 (12) :3661-3688
[9]  
Huisgen R., 1963, Angew. Chem. Int. Ed, V2, P565, DOI [10.1002/anie.196305651, DOI 10.1002/ANIE.196305651]
[10]   Cross-linking reaction of segregated microdomains formed by diblock copolymer films [J].
Ishizu, K ;
Hosokawa, T ;
Tsubaki, K .
EUROPEAN POLYMER JOURNAL, 2000, 36 (07) :1333-1338