Issue 32, 2008

Generation of a triplet diradical from a donor–acceptor cross conjugate upon acid-induced electron transfer

Abstract

Enhancement of the electron acceptor ability of a para-quinodiimine unit by double protonation leads to the proton-induced intramolecular electron transfer from the donor unit to the cross-conjugated acceptor, giving rise to ground state triplet diradical reversibly.

Graphical abstract: Generation of a triplet diradical from a donor–acceptor cross conjugate upon acid-induced electron transfer

Supplementary files

Article information

Article type
Communication
Submitted
25 Mar 2008
Accepted
06 May 2008
First published
18 Jun 2008

Chem. Commun., 2008, 3738-3740

Generation of a triplet diradical from a donor–acceptor cross conjugate upon acid-induced electron transfer

M. O. Sandberg, O. Nagao, Z. Wu, M. M. Matsushita and T. Sugawara, Chem. Commun., 2008, 3738 DOI: 10.1039/B804999H

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