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Issue 35, 2013
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Polypeptoids: a model system to study the effect of monomer sequence on polymer properties and self-assembly

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Abstract

As the ability to control the monomer sequence of synthetic polymers increases, new relationships between sequence, polymer structure, and functional properties are being discovered. Recent advances in the sequence control of traditional copolymers, such as polyethylenes and polystyrenes, have led to well controlled primary structures ranging from periodic to more precise sequences. As a result, this unprecedented control in the chemical structure of the polymer has necessitated a reexamination of the role of monomer sequence on polymer properties, such as crystallization and self-assembly. In this review, we summarize the developments in establishing a relationship between a polymer’s sequence and its properties, and we focus on one sequence-specific polymer system in particular: N-substituted glycines, or polypeptoids. Polypeptoid self-assembly has demonstrated remarkably tunable, hierarchical structures, and through this lens, we look to the future “designability” of sequence-specific polymers in general.

Graphical abstract: Polypeptoids: a model system to study the effect of monomer sequence on polymer properties and self-assembly

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Publication details

The article was received on 21 May 2013, accepted on 09 Jul 2013 and first published on 12 Jul 2013


Article type: Review Article
DOI: 10.1039/C3SM51421H
Citation: Soft Matter, 2013,9, 8400-8414
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    Polypeptoids: a model system to study the effect of monomer sequence on polymer properties and self-assembly

    A. M. Rosales, R. A. Segalman and R. N. Zuckermann, Soft Matter, 2013, 9, 8400
    DOI: 10.1039/C3SM51421H

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