Anion binding vs. sulfonamide deprotonation in functionalised ureas
Anion binding vs. sulfonamide deprotonation in functionalised ureas
Sulfonamide groups, commonly used as neutral hydrogen bond donors in a wide variety of anion receptors, deprotonate upon addition of certain basic anionic guests in two simple functionalised ureas.
molecular recognition, receptors, stability, fluoride, sensors, derivatives
61-63
Caltagirone, Claudia
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Bates, Gareth W.
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Gale, Philip A.
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Light, Mark E.
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January 2008
Caltagirone, Claudia
9148afed-6af0-4fcd-b30e-daa3d7765dc0
Bates, Gareth W.
9b7c0c2e-76a1-4e20-870e-1fdbfeeaa36e
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Caltagirone, Claudia, Bates, Gareth W., Gale, Philip A. and Light, Mark E.
(2008)
Anion binding vs. sulfonamide deprotonation in functionalised ureas.
Chemical Communications, (1), .
(doi:10.1039/b713431b).
Abstract
Sulfonamide groups, commonly used as neutral hydrogen bond donors in a wide variety of anion receptors, deprotonate upon addition of certain basic anionic guests in two simple functionalised ureas.
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Published date: January 2008
Keywords:
molecular recognition, receptors, stability, fluoride, sensors, derivatives
Identifiers
Local EPrints ID: 144965
URI: http://eprints.soton.ac.uk/id/eprint/144965
ISSN: 1359-7345
PURE UUID: 4b337ecf-449f-4106-9449-c3bf63054b70
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Date deposited: 15 Apr 2010 13:39
Last modified: 14 Mar 2024 02:44
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Contributors
Author:
Claudia Caltagirone
Author:
Gareth W. Bates
Author:
Philip A. Gale
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