Issue 9, 2014

Stereoselective synthesis of folded luminogens with arene–arene stacking interactions and aggregation-enhanced emission

Abstract

Tetraphenylethene derivatives with a folded Z-conformation and aggregation-enhanced emission characteristics are synthesized from 2-arylbenzophenones. The intramolecular rotation of the folded luminogens is partially suppressed, resulting in improved emission efficiencies in solutions.

Graphical abstract: Stereoselective synthesis of folded luminogens with arene–arene stacking interactions and aggregation-enhanced emission

Supplementary files

Article information

Article type
Communication
Submitted
07 Oct 2013
Accepted
30 Oct 2013
First published
10 Dec 2013

Chem. Commun., 2014,50, 1131-1133

Stereoselective synthesis of folded luminogens with arene–arene stacking interactions and aggregation-enhanced emission

Z. Zhao, B. He, H. Nie, B. Chen, P. Lu, A. Qin and B. Z. Tang, Chem. Commun., 2014, 50, 1131 DOI: 10.1039/C3CC47696K

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