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Coord Chem Rev. 2017 Aug 15;345:281-296. doi: 10.1016/j.ccr.2017.04.004. Epub 2017 Apr 20.

Pyrrole N-H Anion Complexes.

Coordination chemistry reviews

Gabriela I Vargas-Zúñiga, Jonathan L Sessler

Affiliations

  1. Department of Chemistry, The University of Texas at Austin, 105 E. 24 Street, Stop A5300, Austin, Texas 78712-1224, USA.

PMID: 29104304 PMCID: PMC5663291 DOI: 10.1016/j.ccr.2017.04.004

Abstract

Synthetic pyrrole-based anion receptors date back to the 1990s. They have been extensively developed in the context of macrocyclic systems as expanded porphyrins and calixpyrroles, and related systems. The chemistry of open-chain pyrrolic systems is, in many respects, no less venerable. It also has more direct analogy to naturally occurring pyrrole-based anion binding motifs. However, it has not been the subject of a comprehensive review. Presented herein is a summary of efforts devoted to the creation of de novo pyrrole-based receptors, as well as the anion recognition chemistry of naturally occurring pyrrolic systems as prodigiosins and their synthetic analogues.

Keywords: Anion Binding; Hydrogen-bonding; Prodigiosin; Pyrrole; Receptor; Recognition

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