2009
DOI: 10.1002/macp.200990004
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Macromol. Chem. Phys. 5/2009

Abstract: Cover: Chemoselective stepwise coupling between living polymers and a heterobifunctional linking agent renders feasible the synthesis of block copolymers that are not accessible by sequential monomer addition. This facile and efficient synthetic tool resembles the versatility of a Swissarmy knife, being a powerful strategy for accessing welldefined block copolymers. Further details can be found in the article by V. Bellas, M. Rehahn on page 320.

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Cited by 7 publications
(11 citation statements)
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“…The PS-b-PFDMS diblock copolymer was synthesized by sequential living anionic polymerization in glass reactors equipped with break-seals for the addition of the reagents (Scheme 1). [8,11,22] First, styrene was polymerized in cyclohexene at room temperature using the required amount of sec-BuLi. After completed conversion (%12 h), a solution of FS in cyclohexene was added by smashing the breakseal of the corresponding ampoule.…”
Section: Experimental Part Materials and Synthesesmentioning
confidence: 99%
See 1 more Smart Citation
“…The PS-b-PFDMS diblock copolymer was synthesized by sequential living anionic polymerization in glass reactors equipped with break-seals for the addition of the reagents (Scheme 1). [8,11,22] First, styrene was polymerized in cyclohexene at room temperature using the required amount of sec-BuLi. After completed conversion (%12 h), a solution of FS in cyclohexene was added by smashing the breakseal of the corresponding ampoule.…”
Section: Experimental Part Materials and Synthesesmentioning
confidence: 99%
“…[1][2][3][4][5][6][7] Moreover, it counts among the very few metallopolymers accessible by living chain-growth protocols which give access not only to products of defined molar mass and narrow polydispersity but also to a broad variety of copolymer architectures: plenty of PFDMS block copolymers with, e.g., polystyrene (PS), [8][9][10][11] polyisoprene (PI), [12] poly(dimethyl siloxane) (PDMS), [8,12,13] poly(ethylene oxide) (PEO), [14] poly(methyl methacrylate) (PMMA), [15][16][17][18][19][20][21] and poly(2-vinylpyridine) [22] have been synthesized, and they have been shown to develop fascinating morphologies at the nanometer to micrometer scale. [2,7,23] Another important feature of PFDMS is its ability to crystallize.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3] However, its application is limited because of its awful film-forming property, poor cohesion, and low-glass transition temperature, which induce the cumbersome curing process of PDMS and poor mechanical performance. [12][13][14][15] It is very little that block copolymers containing polysiloxanes were prepared, because polysiloxanes is susceptible to many reagents such as acid and alkali. Specifically, hybrid polymers containing PDMS have been reported for many different applications such as nanotechnology, electronics, filtration, two-dimensional liquid chromatography, and adsorption, among many others.…”
Section: Introductionmentioning
confidence: 99%
“…Polylactide with Different Architectures Anthony J. Ryan et al [9] Block Copolymer Synthesis via Chemoselective Stepwise Coupling Reactions Matthias Rehahn et al [10] Fabrication of Large-Area, Transferable Colloidal Monolayers Utilizing SelfAssembly at the Air/Water Interface Ulrich Jonas et al [11] development of MRE is supported by several newly Already two years ago we launched our news service, MaterialsViews, to keep you updated on the newest developments in the field of materials science, both in print and as an online service, MaterialsViews.com. The print edition is published in many Wiley materials science journals and informs you about highlights from our journals and books in this area, while the online version offers even more news and information on a daily basis.…”
Section: Colloidal Nanoreactormentioning
confidence: 99%