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Single‐Chain Self‐Folding of Synthetic Polymers Induced by Metal–Ligand Complexation
Author(s) -
Willenbacher Johannes,
Altintas Ozcan,
Roesky Peter W.,
BarnerKowollik Christopher
Publication year - 2014
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.201300594
Subject(s) - triphenylphosphine , azide , polymer , ligand (biochemistry) , polymer chemistry , cycloaddition , chemistry , metal , folding (dsp implementation) , copper , atom transfer radical polymerization , combinatorial chemistry , copolymer , catalysis , organic chemistry , biochemistry , receptor , electrical engineering , engineering
The controlled folding of a single polymer chain is for the first time realized by metal‐ complexation. α,ω‐Bromine functional linear polymers are prepared via activators regenerated by electron transfer (ARGET) ATRP ( M ¯ n ,SEC = 5900 g mol −1 , Đ = 1.07 and 12 000 g mol −1 , Đ = 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 ¯ n ,SEC = 6600 g mol −1 , Đ = 1.07, and 12 800 g mol −1 , Đ = 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 1 H and 31 P{ 1 H} NMR experiments, SEC, and DLS unambiguously evidence the efficient formation of SCMCs via metal ligand complexation.
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