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Structural and molecular recognition studies with acyclic anion receptors

Structural and molecular recognition studies with acyclic anion receptors
Structural and molecular recognition studies with acyclic anion receptors
Acyclic molecules containing amides, ureas, and pyrrole groups have proven to be effective and selective anion-binding agents. In this Account, the structural chemistry of isophthalamide anion complexes, ortho-phenylenediamine based bis-ureas, and amidopyrroles, as well as anion-triggered deprotonation processes in neutral anion receptor systems, are discussed.
solid-state, carboxylate complexation, binding properties, deprotonation, urea, prodigiosin, chloride, analogs, sensors, family
0001-4842
465-475
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943

Gale, Philip A. (2006) Structural and molecular recognition studies with acyclic anion receptors. Accounts of Chemical Research, 39 (7), 465-475. (doi:10.1021/ar040237q).

Record type: Article

Abstract

Acyclic molecules containing amides, ureas, and pyrrole groups have proven to be effective and selective anion-binding agents. In this Account, the structural chemistry of isophthalamide anion complexes, ortho-phenylenediamine based bis-ureas, and amidopyrroles, as well as anion-triggered deprotonation processes in neutral anion receptor systems, are discussed.

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Published date: 2006
Keywords: solid-state, carboxylate complexation, binding properties, deprotonation, urea, prodigiosin, chloride, analogs, sensors, family

Identifiers

Local EPrints ID: 44445
URI: http://eprints.soton.ac.uk/id/eprint/44445
ISSN: 0001-4842
PURE UUID: 9e6c633f-a887-4146-b91d-b958c465a130
ORCID for Philip A. Gale: ORCID iD orcid.org/0000-0001-9751-4910

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Date deposited: 06 Mar 2007
Last modified: 17 Dec 2019 01:52

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Author: Philip A. Gale ORCID iD

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