Issue 6, 1999

Sterically protected 1,2,3-dithiazolyl radicals: preparation and structural characterization of 4-chloro-5-pentafluorophenyl-1,2,3-dithiazolyl

Abstract

Steric protection afforded by a pentafluorophenyl group at the 5-position facilitates the first isolation and structural characterization of a monocyclic 1,2,3-dithiazolyl as its S–S bonded dimer.

Article information

Article type
Paper

Chem. Commun., 1999, 531-532

Sterically protected 1,2,3-dithiazolyl radicals: preparation and structural characterization of 4-chloro-5-pentafluorophenyl-1,2,3-dithiazolyl

T. M. Barclay, A. Wallace Cordes, L. Beer, R. T. Oakley, K. E. Preuss, N. J. Taylor and R. W. Reed, Chem. Commun., 1999, 531 DOI: 10.1039/A809951K

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