Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges

Schmidt, B. V.K.J. , Fechler, N., Falkenhagen, J. and Lutz, J.-F. (2011) Controlled folding of synthetic polymer chains through the formation of positionable covalent bridges. Nature Chemistry, 3(3), pp. 234-238. (doi:10.1038/nchem.964) (PMID:21336330)

Full text not currently available from Enlighten.

Abstract

Covalent bridges play a crucial role in the folding process of sequence-defined biopolymers. This feature, however, has not been recreated in synthetic polymers because, apart from some simple regular arrangements (such as block co-polymers), these macromolecules generally do not exhibit a controlled primary structure—that is, it is difficult to predetermine precisely the sequence of their monomers. Herein, we introduce a versatile strategy for preparing foldable linear polymer chains. Well-defined polymers were synthesized by the atom transfer radical polymerization of styrene. The controlled addition of discrete amounts of protected maleimide at precise times during the synthesis enabled the formation of polystyrene chains that contained positionable reactive alkyne functions. Intramolecular reactions between these functions subsequently led to the formation of different types of covalently folded polymer chains. For example, tadpole (P-shaped), pseudocyclic (Q-shaped), bicyclic (8-shaped) and knotted (α-shaped) macromolecular origamis were prepared in a relatively straightforward manner.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Schmidt, Dr Bernhard
Authors: Schmidt, B. V.K.J., Fechler, N., Falkenhagen, J., and Lutz, J.-F.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Nature Chemistry
Publisher:Nature Publishing Group
ISSN:1755-4330
ISSN (Online):1755-4349
Published Online:23 January 2011

University Staff: Request a correction | Enlighten Editors: Update this record