Single-Chain Self-Folding of Synthetic Polymers Induced by Metal-Ligand Complexation

被引:53
|
作者
Willenbacher, Johannes [1 ,2 ]
Altintas, Ozcan [1 ,2 ]
Roesky, Peter W. [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 Anorgan Chem, D-76131 Karlsruhe, Germany
关键词
macroligands; metal complexes; single-chain folding; synthetic proteins; CLICK CHEMISTRY; RADICAL POLYMERIZATION; STAR POLYMERS; NANOPARTICLES; CARBONYLATION; POLYSTYRENE; COVALENT; RAFT;
D O I
10.1002/marc.201300594
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The controlled folding of a single polymer chain is for the first time realized by metal-complexation. alpha,omega-Bromine functional linear polymers are prepared via activators regenerated by electron transfer (ARGET) ATRP ((M) over bar (n, SEC) = 5900 g mol(-1), D = 1.07 and 12 000 g mol(-1), D = 1.06) and the end groups of the polymers are subsequently converted to azide functionalities. A copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is carried out in the presence of a novel triphenylphosphine ligand and the polymers to afford homotelechelic bis-triphenylphosphine polymeric-macroligands (MLs) ((M) over bar (n, SEC) = 6600 g mol(-1), D = 1.07, and 12 800 g mol(-1), D = 1.06). Single-chain metal complexes (SCMCs) are formed in the presence of Pd(II) ions in highly diluted solution at ambient temperature. The results derived via H-1 and P-31{H-1} NMR experiments, SEC, and DLS unambiguously evidence the efficient formation of SCMCs via metal ligand complexation.
引用
收藏
页码:45 / 51
页数:7
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