Issue 7, 2002
From the journal:

Chemical Communications

Solution and solid-state studies of 3,4-dichloro-2,5-diamidopyrroles: formation of an unusual anionic narcissistic dimer†

Salvatore Camiolo,a   Philip A. Gale,*a   Michael B. Hursthouse,a   Mark E. Lighta  and  Andy J. Shia  

* Corresponding authors

a Department of Chemistry, University of Southampton, Southampton, UK
E-mail: philip.gale@soton.ac.uk
Fax: +44 23 80596805
Tel: +44 23 80593332

Abstract

3,4-Dichoro-1H-pyrrole-2,5-dicarboxylic acid bis-phenylamide 3 and 3,4-dichoro-1H-pyrrole-2,5-dicarboxylic acid bis-butylamide 4 have been prepared and shown to deprotonate in the presence of basic anions: the X-ray crystal structure of the tetrabutylammonium salt of 3-H+ reveals the formation of a dimer in the solid state.

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Article information

DOI
https://doi.org/10.1039/B200980C
Article type
Communication
Submitted
29 Jan 2002
Accepted
21 Feb 2002
First published
12 Mar 2002

Chem. Commun., 2002, 758-759

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Solution and solid-state studies of 3,4-dichloro-2,5-diamidopyrroles: formation of an unusual anionic narcissistic dimer

S. Camiolo, P. A. Gale, M. B. Hursthouse, M. E. Light and A. J. Shi, Chem. Commun., 2002, 758 DOI: 10.1039/B200980C

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