Supramolecular X- and H-shaped star block copolymers via cyclodextrin-driven supramolecular self-assembly

被引:33
作者
Schmidt, Bernhard V. K. J. [1 ,2 ]
Barner-Kowollik, Christopher [1 ,2 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Karlsruhe Inst Technol KIT, Inst Biol Grenzaflachen, D-76344 Eggenstein Leopoldshafen, Germany
关键词
END-FUNCTIONALIZED POLYMERS; TRIBLOCK COPOLYMERS; INCLUSION COMPLEXATION; RAFT POLYMERIZATION; CLICK CHEMISTRY; DRUG-DELIVERY; DIBLOCK; ARCHITECTURE; LIGHT; ATRP;
D O I
10.1039/c3py01580g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A wide variety of novel complex macromolecular X- and H-shaped star block copolymers based on supramolecular cyclodextrin (CD)/adamantane interactions are reported. Mid-chain adamantyl poly(N,N-dimethylacrylamide) (PDMA; M-n = 12 000 g mol(-1), D = 1.10), poly(N,N-diethylacrylamide) (PDEA; M-n = 5400 g mol(-1), D = 1.08) and P(DEA-b-DMA) (M-n = 10 400 g mol(-1), D = 1.13) as well as double adamantyl end functionalized PDMA (M-n = 6400 g mol(-1), D = 1.06) and PDEA (M-n = 6800 g mol(-1), D = 1.11) are synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization. Furthermore, mid-chain beta-CD functionalized PDMA (M-n = 10 200 g mol(-1), D = 1.26), PDEA (M-n = 11 100 g mol(-1), D = 1.30) and P(DEA-b-DMA) (M-n = 7600 g mol(-1), D = 1.26) are synthesized via a combination of RAFT polymerization and copper(I) catalyzed azide alkyne cycloaddition. Subsequently, the formation of the target architectures via supramolecular association of CD- and adamantyl-functionalized building blocks is evidenced via nuclear Overhauser enhancement spectroscopy and dynamic light scattering. Furthermore, the temperature responsive behavior of the formed star block copolymers is investigated.
引用
收藏
页码:2461 / 2472
页数:12
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