Issue 8, 1992

Synthesis and characterization of new conjugation-extended viologens involving a central aromatic linking group

Abstract

New viologens, in which two pyridinium moieties are linked by a central five-membered heteroaromatic or phenylene framework, giving stable radical cations on single electron reduction and showing an intense fluorescence emission are efficiently synthesized and characterized.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 620-622

Synthesis and characterization of new conjugation-extended viologens involving a central aromatic linking group

K. Takahashi, T. Nihira, K. Akiyama, Y. Ikegami and E. Fukuyo, J. Chem. Soc., Chem. Commun., 1992, 620 DOI: 10.1039/C39920000620

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.

Spotlight

Advertisements