Issue 4, 2003

Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonation

Abstract

Two new pyrrole 2,5-diamide clefts have been synthesized containing 4-nitrophenyl or 3,5-dinitrophenyl groups appended to the amide positions. The 3,5-dinitrophenyl derivative has been shown to deprotonate in the presence of fluoride, which in acetonitrile solution, gives rise to a deep blue colour.

Graphical abstract: Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonation

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2002
Accepted
16 Dec 2002
First published
28 Jan 2003

Org. Biomol. Chem., 2003,1, 741-744

Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonation

S. Camiolo, P. A. Gale, M. B. Hursthouse and M. E. Light, Org. Biomol. Chem., 2003, 1, 741 DOI: 10.1039/B210848H

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