The University of Southampton
University of Southampton Institutional Repository

Fluorescent carbazolylurea- and carbazolylthiourea-based anion receptors and sensors

Fluorescent carbazolylurea- and carbazolylthiourea-based anion receptors and sensors
Fluorescent carbazolylurea- and carbazolylthiourea-based anion receptors and sensors
A series of carbazolylurea- and carbazolylthiourea-based receptors have been synthesised and their anion complexation and fluorescence properties were studied. The urea compounds show selectivity for oxo-anion complexation over chloride and the fluorescence of compound 1 is selectively quenched by benzoate anions in DMSO/0.5% water. However, the thiourea compounds show reduced anion affinities compared to the urea analogues.
anion binding, indole, hydrogen bonding, crystallography
1061-0278
647-652
Hiscock, Jennifer R.
99a8a34c-a869-48e2-b713-1e69e4741032
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Caltagirone, Claudia
9148afed-6af0-4fcd-b30e-daa3d7765dc0
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161
Hiscock, Jennifer R.
99a8a34c-a869-48e2-b713-1e69e4741032
Gale, Philip A.
c840b7e9-6847-4843-91af-fa0f8563d943
Caltagirone, Claudia
9148afed-6af0-4fcd-b30e-daa3d7765dc0
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Light, Mark E.
cf57314e-6856-491b-a8d2-2dffc452e161

Hiscock, Jennifer R., Gale, Philip A., Caltagirone, Claudia, Hursthouse, Michael B. and Light, Mark E. (2010) Fluorescent carbazolylurea- and carbazolylthiourea-based anion receptors and sensors. Supramolecular Chemistry, 22 (11), 647-652. (doi:10.1080/10610271003637087).

Record type: Article

Abstract

A series of carbazolylurea- and carbazolylthiourea-based receptors have been synthesised and their anion complexation and fluorescence properties were studied. The urea compounds show selectivity for oxo-anion complexation over chloride and the fluorescence of compound 1 is selectively quenched by benzoate anions in DMSO/0.5% water. However, the thiourea compounds show reduced anion affinities compared to the urea analogues.

This record has no associated files available for download.

More information

Published date: November 2010
Keywords: anion binding, indole, hydrogen bonding, crystallography

Identifiers

Local EPrints ID: 170325
URI: http://eprints.soton.ac.uk/id/eprint/170325
ISSN: 1061-0278
PURE UUID: 9fb52539-563b-424a-a43d-897cf157d957
ORCID for Philip A. Gale: ORCID iD orcid.org/0000-0001-9751-4910
ORCID for Mark E. Light: ORCID iD orcid.org/0000-0002-0585-0843

Catalogue record

Date deposited: 05 Jan 2011 13:52
Last modified: 14 Mar 2024 02:44

Export record

Altmetrics

Contributors

Author: Jennifer R. Hiscock
Author: Philip A. Gale ORCID iD
Author: Claudia Caltagirone
Author: Mark E. Light ORCID iD

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.

×