Issue 37, 2017

An aryl-triazole foldamer containing a 1,8-naphthalimide fluorescent motif for monitoring and enhancing the anion-induced folding

Abstract

A novel aryl-triazole foldamer incorporating a 1,8-naphthalimide motif was designed and synthesized. 1H NMR, UV-vis and fluorescence spectroscopic titration experiments with halide anions (Cl, Br, I) demonstrated that the π–π stacking interaction of 1,8-naphthalimide building blocks could largely enhance the folding and anion binding of the foldamer.

Graphical abstract: An aryl-triazole foldamer containing a 1,8-naphthalimide fluorescent motif for monitoring and enhancing the anion-induced folding

Supplementary files

Article information

Article type
Communication
Submitted
14 Jul 2017
Accepted
01 Sep 2017
First published
01 Sep 2017

Org. Biomol. Chem., 2017,15, 7747-7752

An aryl-triazole foldamer containing a 1,8-naphthalimide fluorescent motif for monitoring and enhancing the anion-induced folding

L. Yang, Y. Wang, Y. Che and H. Jiang, Org. Biomol. Chem., 2017, 15, 7747 DOI: 10.1039/C7OB01736G

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