Issue 93, 2013

Chiral suprastructures of asymmetric oligothiophene-hybrids induced by a single proline

Abstract

Oligothiophene–proline hybrids were synthesized via click-reaction showing intriguing self-assembly behavior in an aqueous environment by forming chiral superstructures, whose helicity is controlled by the configuration of the amino acid moiety.

Graphical abstract: Chiral suprastructures of asymmetric oligothiophene-hybrids induced by a single proline

Supplementary files

Article information

Article type
Communication
Submitted
28 Jun 2013
Accepted
29 Sep 2013
First published
30 Sep 2013

Chem. Commun., 2013,49, 10929-10931

Chiral suprastructures of asymmetric oligothiophene-hybrids induced by a single proline

A. Digennaro, H. Wennemers, G. Joshi, S. Schmid, E. Mena-Osteritz and P. Bäuerle, Chem. Commun., 2013, 49, 10929 DOI: 10.1039/C3CC44861D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements