2,7-functionalized indoles as receptors for anions
2,7-functionalized indoles as receptors for anions
A series of 2,7-functionalized indoles have been synthesized with appended amide and/or urea or thiourea groups. Anion complexation studies show a marked difference in the mode of interaction of carboxylates with indole-ureas vs indole-amides.
conformation, solid-state, molecular receptor, recognition, chemistry, stability, binding-properties, highlights, coordination, macrocycles
8921-8927
Bates, Gareth W.
9b7c0c2e-76a1-4e20-870e-1fdbfeeaa36e
Triyanti, (No initials)
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Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Albrecht, Markus
e08838e2-b58f-47d4-9bb9-963f70be5e77
Gale, Philip A.
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2007
Bates, Gareth W.
9b7c0c2e-76a1-4e20-870e-1fdbfeeaa36e
Triyanti, (No initials)
e7e024a3-64bb-4af9-8f17-aa432db67d21
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Albrecht, Markus
e08838e2-b58f-47d4-9bb9-963f70be5e77
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Bates, Gareth W., Triyanti, (No initials), Light, Mark E., Albrecht, Markus and Gale, Philip A.
(2007)
2,7-functionalized indoles as receptors for anions.
Journal of Organic Chemistry, 72 (23), .
(doi:10.1021/jo701702p).
Abstract
A series of 2,7-functionalized indoles have been synthesized with appended amide and/or urea or thiourea groups. Anion complexation studies show a marked difference in the mode of interaction of carboxylates with indole-ureas vs indole-amides.
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Published date: 2007
Keywords:
conformation, solid-state, molecular receptor, recognition, chemistry, stability, binding-properties, highlights, coordination, macrocycles
Identifiers
Local EPrints ID: 54241
URI: http://eprints.soton.ac.uk/id/eprint/54241
ISSN: 0022-3263
PURE UUID: 97c8d7df-52b8-4afa-96a7-784563be07b0
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Date deposited: 31 Jul 2008
Last modified: 16 Mar 2024 03:16
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Contributors
Author:
Gareth W. Bates
Author:
(No initials) Triyanti
Author:
Markus Albrecht
Author:
Philip A. Gale
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