'Twisted' isophthalamide analogues
'Twisted' isophthalamide analogues
Steric interactions in 1,3-dicarboxamidoanthraquinones have been employed to 'twist' isophthalamide-like anion binding sites; the crystal structure of the fluoride complex of a bis-3,5-dichlorophenylamide derivative shows the receptor acting as a 'hydrogen-bonding corner' in a '2 + 2' fluoride containing molecular box.
anion recognition, ion-pair, anthraquinone, receptors, binding, versatile, sensors, urea
734-736
Brooks, Simon J.
fcf66c9a-5e4d-47cf-bc9f-e7c8886a061a
Evans, Louise S.
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Gale, Philip A.
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Hursthouse, Michael B.
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Light, Mark E.
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2005
Brooks, Simon J.
fcf66c9a-5e4d-47cf-bc9f-e7c8886a061a
Evans, Louise S.
c9b34cb4-14cc-4587-a145-abdb0a74ead7
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Brooks, Simon J., Evans, Louise S., Gale, Philip A., Hursthouse, Michael B. and Light, Mark E.
(2005)
'Twisted' isophthalamide analogues.
Chemical Communications, 2005 (6), .
(doi:10.1039/b413654c).
Abstract
Steric interactions in 1,3-dicarboxamidoanthraquinones have been employed to 'twist' isophthalamide-like anion binding sites; the crystal structure of the fluoride complex of a bis-3,5-dichlorophenylamide derivative shows the receptor acting as a 'hydrogen-bonding corner' in a '2 + 2' fluoride containing molecular box.
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Published date: 2005
Keywords:
anion recognition, ion-pair, anthraquinone, receptors, binding, versatile, sensors, urea
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Local EPrints ID: 20738
URI: http://eprints.soton.ac.uk/id/eprint/20738
ISSN: 1359-7345
PURE UUID: 7b50c36e-da65-468c-9511-b764b508d483
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Date deposited: 02 Mar 2006
Last modified: 16 Mar 2024 03:16
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Author:
Simon J. Brooks
Author:
Louise S. Evans
Author:
Philip A. Gale
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