ABC-type miktoarm star terpolymers accessed by H-bonding driven supramolecular self-assembly

被引：21
|
作者：
Altintas, Ozcan [1 ,2 ]
Schulze-Suenninghausen, David [2 ,3 ]
Luy, Burkhard [2 ,3 ]
Barner-Kowollik, Christopher [1 ,2 ]
机构：
[1] Karlsruhe Inst Technol, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Karlsruhe Inst Technol, Inst Biol Grenzflachen, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Inst Organ Chem, D-76131 Karlsruhe, Germany
来源：
EUROPEAN POLYMER JOURNAL | 2015年 / 62卷
关键词：
Supramolecular Architectures; Miktoarms Star Polymers; Hydrogenbonding; DOSY; DLS; FACILE PREPARATION; POLYMERS; COPOLYMERS;
D O I：
10.1016/j.eurpolymj.2014.04.006
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 supramolecular ABC-type miktoarm star polymer was prepared using a Hamilton wedge (HW) mid-chain functionalized polyethylene glycol-b-polystyrene (PEG-HW-PS) block copolymer and an alpha-cyanuric acid (CA) chain-end functional linear homopolymer poly(n-butylacrylate) (CA-PnBA). The PEG-HW-PS element prepared via a combination of atom transfer radical polymerization (ATRP) and copper-catalyzed azide alkyne cycloaddition (CuAAC) (M-n = 13,700 g mol(-1), PDI = 1.04). The CA-PnBA strand was synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization (M-n = 11,300 g mol(-1), PDI = 1.06). The quantitative formation of a well-defined supramolecular ABC-type miktoarm star polymer was unambiguously proven via proton nuclear magnetic resonance (H-1 NMR) spectroscopy, diffusion ordered NMR spectroscopy (DOSY) and dynamic light scattering (DLS) analyses. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码：409 / 417
页数：9
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