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
465-475
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
2006
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), .
(doi:10.1021/ar040237q).
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
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Local EPrints ID: 44445
URI: http://eprints.soton.ac.uk/id/eprint/44445
ISSN: 0001-4842
PURE UUID: 9e6c633f-a887-4146-b91d-b958c465a130
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Date deposited: 06 Mar 2007
Last modified: 16 Mar 2024 03:16
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Author:
Philip A. Gale
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