Issue 3, 2017

Unexpected right-handed helical nanostructures co-assembled from l-phenylalanine derivatives and achiral bipyridines

Abstract

The construction of chiral supramolecular systems with desirable handedness is of great importance in materials science, chemistry, and biology since chiral nanostructures exhibit fascinating photophysical properties and unique biological effects. Herein, we report that achiral bipyridines can co-assemble with L-phenylalanine derivatives into unexpected right-handed helical nanostructures rather than a left-handed helix via intermolecular hydrogen bonding interactions formed between the pyridyl and carboxylic groups. This study opens up a route to develop chiral nanostructures with desirable handedness via the co-assembly of simple molecular building blocks and provides a straightforward insight into the chirality control of nanostructures in supramolecular systems.

Graphical abstract: Unexpected right-handed helical nanostructures co-assembled from l-phenylalanine derivatives and achiral bipyridines

Supplementary files

Article information

Article type
Edge Article
Submitted
29 Oct 2016
Accepted
03 Jan 2017
First published
04 Jan 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2017,8, 1769-1775

Unexpected right-handed helical nanostructures co-assembled from L-phenylalanine derivatives and achiral bipyridines

G. Liu, J. Liu, C. Feng and Y. Zhao, Chem. Sci., 2017, 8, 1769 DOI: 10.1039/C6SC04808K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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