Issue 93, 2013
From the journal:

Chemical Communications

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

Angela Digennaro,a   Helma Wennemers,b   Gururaj Joshi,b   Sylvia Schmid,a   Elena Mena-Osteritz*a  and  Peter Bäuerle*a  

* Corresponding authors

a Institute of Organic Chemistry II and Advanced Materials, University of Ulm, Germany
E-mail: elena.mena-osteritz@uni-ulm.de, peter.baeuerle@uni-ulm.de

b Laboratory of Organic Chemistry, D-CHAB, ETH Zürich, Switzerland

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

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Article information

DOI
https://doi.org/10.1039/C3CC44861D
Article type
Communication
Submitted
28 Jun 2013
Accepted
29 Sep 2013
First published
30 Sep 2013

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

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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

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