Issue 10, 2014

Twisted intramolecular charge transfer, aggregation-induced emission, supramolecular self-assembly and the optical waveguide of barbituric acid-functionalized tetraphenylethene

Abstract

A red-emissive barbituric acid-functionalized tetraphenylethene derivative (TPE-HPh-Bar) was designed and synthesized. TPE-HPh-Bar exhibits the effect of twisted intramolecular charge transfer due to the interaction of its donor and acceptor units. Whereas TPE-HPh-Bar emits faintly in solution, it becomes a strong emitter in the aggregated state, demonstrating a phenomenon of aggregation-induced emission. TPE-HPh-Bar can self-assemble into nanospheres upon natural evaporation of its solutions. In the presence of melamine, nanorods and (un)sealed nanotubes are formed, the content of which depends on the melamine amount. The crystalline nanorods of TPE-HPh-Bar grown from diethyl ether/hexane solution exhibit a good optical waveguiding effect with a low optical loss (0.137 dB μm−1). Such attributes make the material to find wide applications in many areas such as biological imaging and optoelectronic nano-devices.

Graphical abstract: Twisted intramolecular charge transfer, aggregation-induced emission, supramolecular self-assembly and the optical waveguide of barbituric acid-functionalized tetraphenylethene

Supplementary files

Article information

Article type
Paper
Submitted
01 Nov 2013
Accepted
10 Dec 2013
First published
11 Dec 2013

J. Mater. Chem. C, 2014,2, 1801-1807

Twisted intramolecular charge transfer, aggregation-induced emission, supramolecular self-assembly and the optical waveguide of barbituric acid-functionalized tetraphenylethene

E. Wang, J. W. Y. Lam, R. Hu, C. Zhang, Y. S. Zhao and B. Z. Tang, J. Mater. Chem. C, 2014, 2, 1801 DOI: 10.1039/C3TC32161D

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