Issue 12, 2016

Innocent BN bond substitution in anthracene derivatives

Abstract

Extended azaborine heterocycles are promising biomedical and electronic materials. Herein we report the synthesis of a novel family of azaborine anthracene derivatives and their structural, electrochemical and spectroscopic characterization. We observe that the properties of these materials are remarkably similar to the parent hydrocarbons, suggesting the innocence of the CC to BN bond substitution. Our results support the prospective stability to long-term usage of extended azaborines and the feasibility of using such materials in device applications.

Graphical abstract: Innocent BN bond substitution in anthracene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
09 Nov 2015
Accepted
23 Feb 2016
First published
23 Feb 2016

Org. Biomol. Chem., 2016,14, 3256-3263

Author version available

Innocent BN bond substitution in anthracene derivatives

H. L. van de Wouw, J. Y. Lee, M. A. Siegler and R. S. Klausen, Org. Biomol. Chem., 2016, 14, 3256 DOI: 10.1039/C5OB02309B

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