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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.
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页码:45 / 51
页数:7
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