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Issue 7, 2012
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Controlled folding of polystyrene single chains: design of asymmetric covalent bridges

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Abstract

α-Shaped polystyrene origamis with variable sizes and loop diameters were synthesized using a simple folding strategy. Linear polystyrene precursors containing precisely incorporated reactive functions (i.e. alkyne and activated ester moieties) were first synthesized by sequence-controlled copolymerization of styrene (donor comonomer) with functional N-substituted maleimides (acceptor comonomers). These copolymers were prepared by nitroxide mediated polymerization in the presence of a commercially available alkoxyamine (i.e. BlocBuilder® MA). Discrete amounts (i.e. one molar equivalent as compared to the alkoxyamine) of triisopropylsilyl-protected N-propargyl maleimide and pentafluorophenyl 4-maleimidobenzoate were added at precise moments during the polymerization of a large excess of styrene. Due to the kinetically favored cross-propagation of donor and acceptor comonomers, the N-substituted maleimides were incorporated in precise regions of the polystyrene chains. Linear precursors with variable chain-lengths and sequence distributions were synthesized and characterized using 1H NMR, size exclusion chromatography (SEC) and FT-IR spectroscopy. Afterwards the chains were folded in solution using a two-step strategy. The pentafluorophenyl activated ester moieties were first reacted with 11-azido-3,6,9-trioxaundecan-1-amine, thus leading to azide-functionalized polymers. Subsequently, intramolecular azide–alkyne Huisgen cycloadditions were performed in dilute DMF solutions in the presence of a copper-based catalyst. SEC, 1H NMR, and FT-IR measurements indicated the formation of folded polymer chains containing asymmetric covalent bridges.

Graphical abstract: Controlled folding of polystyrene single chains: design of asymmetric covalent bridges

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Publication details

The article was received on 31 Oct 2011, accepted on 20 Nov 2011 and first published on 07 Dec 2011


Article type: Paper
DOI: 10.1039/C1PY00514F
Citation: Polym. Chem., 2012,3, 1796-1802
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    Controlled folding of polystyrene single chains: design of asymmetric covalent bridges

    M. Zamfir, P. Theato and J. Lutz, Polym. Chem., 2012, 3, 1796
    DOI: 10.1039/C1PY00514F

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