Issue 24, 2018

Tuning the fluorescence of tetraphenylethylene in dilute solutions via modulating multiple-hydrogen-bonding interactions between a Hamilton receptor and cyanuric acid

Abstract

Four Hamilton receptors and four cyanuric acid modules were introduced into the tetraphenylethylene skeleton to form HTPE and CTPE, respectively. Upon 1 : 1 mixing of HTPE and CTPE in apolar dilute solution, a self-assembled supramolecular network was formed via multiple intermolecular hydrogen bonding interactions. The intramolecular rotation of phenyls in TPE skeletons was restricted, and thus the system became highly luminescent. Upon the addition of a hydrogen bonding competitive solvent to destroy the network, the fluorescence emission was substantially quenched. Besides, the fluorescence of the system could be further tuned by the addition of Cu2+ and other metal ions.

Graphical abstract: Tuning the fluorescence of tetraphenylethylene in dilute solutions via modulating multiple-hydrogen-bonding interactions between a Hamilton receptor and cyanuric acid

Supplementary files

Article information

Article type
Communication
Submitted
06 abr. 2018
Accepted
21 may. 2018
First published
21 may. 2018

Org. Biomol. Chem., 2018,16, 4429-4432

Tuning the fluorescence of tetraphenylethylene in dilute solutions via modulating multiple-hydrogen-bonding interactions between a Hamilton receptor and cyanuric acid

D. Wang, D. Zhu, W. Ding, M. Xue and Y. Yang, Org. Biomol. Chem., 2018, 16, 4429 DOI: 10.1039/C8OB00814K

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