Anion binding properties of 5,5’-dicarboxamido-dipyrrolylmethanes
Anion binding properties of 5,5’-dicarboxamido-dipyrrolylmethanes
A series of a 5,5’-dicarboxamidodipyrrolylmethanes have been synthesized and in some cases crystallographically characterized. Proton NMR titrations have revealed that these compounds, that contain only four neutral hydrogen bond donors and are acyclic, selectively bind anions in very competitive solvent media such as DMSO-d6/water mixtures.
dipyrrolylmethanes, phosphate, anion binding, supramolecular chemistry
2935-2941
Vega, Ismael El Drubi
b9c8751d-ad70-4a6a-b324-394a3747c206
Gale, Philip A.
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Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Vega, Ismael El Drubi
b9c8751d-ad70-4a6a-b324-394a3747c206
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Vega, Ismael El Drubi, Gale, Philip A., Hursthouse, Michael B. and Light, Mark E.
(2004)
Anion binding properties of 5,5’-dicarboxamido-dipyrrolylmethanes.
Organic & Biomolecular Chemistry, 2 (20), .
(doi:10.1039/b409115a).
(Submitted)
Abstract
A series of a 5,5’-dicarboxamidodipyrrolylmethanes have been synthesized and in some cases crystallographically characterized. Proton NMR titrations have revealed that these compounds, that contain only four neutral hydrogen bond donors and are acyclic, selectively bind anions in very competitive solvent media such as DMSO-d6/water mixtures.
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Submitted date: 15 June 2004
Keywords:
dipyrrolylmethanes, phosphate, anion binding, supramolecular chemistry
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Local EPrints ID: 15718
URI: http://eprints.soton.ac.uk/id/eprint/15718
ISSN: 1477-0520
PURE UUID: 31acc8a5-d0c2-4af7-b48a-f8ab842634bb
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Date deposited: 24 May 2005
Last modified: 16 Mar 2024 03:15
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Author:
Ismael El Drubi Vega
Author:
Philip A. Gale
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