Issue 5, 1992

2,4,6-Tris(4,5-diisopropyl-1,3-dithiol-2-ylidene)cyclohexane-1,3,5-trione: synthesis, X-ray crystal structure and amphoteric redox properties of a highly delocalised heterocyclic π-system

Abstract

The title compound 1 is synthesised by treatment of 1,3,5-trihydroxybenzene with 2-methylthio-4,5-di-n-propyl-1,3-dithiolium iodide in the presence of pyridine; the X-ray crystal structure of 1 reveals a highly delocalised π-system with strongly bonding intramolecular S ⋯ O interactions; four-stage, amphoteric redox behaviour is observed by cyclic voltammetry.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 401-402

2,4,6-Tris(4,5-diisopropyl-1,3-dithiol-2-ylidene)cyclohexane-1,3,5-trione: synthesis, X-ray crystal structure and amphoteric redox properties of a highly delocalised heterocyclic π-system

M. A. Coffin, M. R. Bryce and W. Clegg, J. Chem. Soc., Chem. Commun., 1992, 401 DOI: 10.1039/C39920000401

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