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Issue 6, 2017
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Orthogonally reactive amino acids and end groups in NCA polymerization

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Abstract

Functional amino acids whose reactivity is compatible with the polymerization of α-amino acid-N-carboxyanhydrides (NCAs) have received a lot of attention in recent years. The appeal of these reactive monomers lies in the fact that the resulting polymers can be easily modified in one controlled post-polymerization step, leading to a variety of polypeptidic materials like helical non-natural polycations or glycopeptides. This review highlights recent developments in the field and focuses on the different reactive groups like alkynes, alkenes, azides, chlorides and S-alkylsulfonyls. Furthermore, the modifications after polymerization are discussed, pointing out advantages and challenges. Besides orthogonal functionalities in the side chain, different approaches are summarized to modify α- and ω-chain ends with orthogonal functionalities for grafting to and grafting from applications. Thus, new materials can be produced through mild modifications as presented. Finally, we also highlight the development of orthogonally reactive NCAs for the synthesis of polypeptoids, a field that is relatively unexplored, but offers great possibilities for example for polypept(o)idic hybrid materials.

Graphical abstract: Orthogonally reactive amino acids and end groups in NCA polymerization

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Article information


Submitted
17 Oct 2016
Accepted
15 Dec 2016
First published
15 Dec 2016

Polym. Chem., 2017,8, 957-971
Article type
Review Article

Orthogonally reactive amino acids and end groups in NCA polymerization

D. Huesmann, K. Klinker and M. Barz, Polym. Chem., 2017, 8, 957
DOI: 10.1039/C6PY01817C

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