The University of Southampton
University of Southampton Institutional Repository

Isophthalamides and 2,6-dicarboxamidopyridines with pendant indole groups: a 'twisted' binding mode for selective fluoride recognition

Record type: Article

Two cleft-like anion receptors have been synthesised that contain indole hydrogen-bond donors and show fluoride selectively in a DMSO–water solution with crystallographic studies showing a ‘twisted’ binding mode for fluoride in the solid state. Twisted structures have long been of particular interest to the supramolecular chemistry community. From early work on metal templated helices1 through more recent work on foldamers2 and organic helical structures,3 these species are not only elegantly designed but can also play roles in molecular recognition and sensing.

Full text not available from this repository.

Citation

Bates, G.W., Gale, P.A. and Light, M.E. (2007) Isophthalamides and 2,6-dicarboxamidopyridines with pendant indole groups: a 'twisted' binding mode for selective fluoride recognition Chemical Communications, (21), pp. 2121-2123. (doi:10.1039/b703905k).

More information

Published date: 2007
Keywords: macrocycles, molecular receptor, chloride, conformational control, foldamers, anion, phosphate, stability

Identifiers

Local EPrints ID: 54240
URI: http://eprints.soton.ac.uk/id/eprint/54240
ISSN: 1359-7345
PURE UUID: 3901238d-83d6-47df-a0e9-25e3eb0ed64e
ORCID for P.A. Gale: ORCID iD orcid.org/0000-0001-9751-4910
ORCID for M.E. Light: ORCID iD orcid.org/0000-0002-0585-0843

Catalogue record

Date deposited: 31 Jul 2008
Last modified: 17 Jul 2017 14:36

Export record

Altmetrics

Contributors

Author: G.W. Bates
Author: P.A. Gale ORCID iD
Author: M.E. Light ORCID iD

University divisions


Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×