Issue 13, 2002

Synthesis of diselenadiazafulvalenes and influence of steric strain on their anodic behavior

Abstract

A novel family of π-donor molecules, the diselenadiazafulvalenes (DSeDAFs), is presented. The synthetic approach to these donors, from o-nitroaniline, allows the formation of N,N′-dimethyldibenzoDSeDAF and N,N′-ethylenedibenzoDSeDAF. Comparative electrochemical study of these π-donor molecules demonstrates their excellent donor ability and the stabilizing effect of the ethylene bridge on the cation radical species.

Graphical abstract: Synthesis of diselenadiazafulvalenes and influence of steric strain on their anodic behavior

Supplementary files

Article information

Article type
Paper
Submitted
04 Apr 2002
Accepted
21 May 2002
First published
11 Jun 2002

J. Chem. Soc., Perkin Trans. 1, 2002, 1568-1573

Synthesis of diselenadiazafulvalenes and influence of steric strain on their anodic behavior

Z. <img border="0" src="https://www.rsc.org/images/entities/char_0043_0306.gif" alt="[C with combining breve]" xmlns="http://www.rsc.org/schema/rscart38" />asar, I. Leban, A. M. Maréchal and D. Lorcy, J. Chem. Soc., Perkin Trans. 1, 2002, 1568 DOI: 10.1039/B203317H

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