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A dual-functional tetrakis-imidazolium macrocycle for supramolecular assembly

Serpell, C.J., Cookson, J., Thompson, A.L., Beer, P.D. (2011) A dual-functional tetrakis-imidazolium macrocycle for supramolecular assembly. Chemical Science, 2 (3). pp. 494-500. ISSN 20416520 (ISSN). (doi:10.1039/c0sc00511h) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:49496)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
https://doi.org/10.1039/c0sc00511h

Abstract

A new versatile tetrakis-imidazolium macrocycle for use in supramolecular applications is reported. It displays excellent affinities for p-electron rich neutral guests such as 1,5-dihydroxynaphthalene derivatives and TTF, providing opportunities for the construction of interlocked molecules, as well as exhibiting extensive and potent anion coordination chemistry. © The Royal Society of Chemistry 2011.

Item Type: Article
DOI/Identification number: 10.1039/c0sc00511h
Additional information: Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Chem. Sci. [Field not mapped to EPrints] AD - Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Mansfield Road, Oxford, OX1 3TA, United Kingdom [Field not mapped to EPrints] AD - Johnson Matthey Technology Centre, Blount's Court, Sonning Common, Reading, RG4 9NH, United Kingdom [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints]
Uncontrolled keywords: Anion coordination, Dihydroxynaphthalenes, Electron-rich, Imidazolium, Interlocked molecules, Macrocycles, Supramolecular assemblies, Tetrakis, Coordination reactions, Supramolecular chemistry, Negative ions
Subjects: Q Science > QD Chemistry
Divisions: Divisions > Division of Natural Sciences > Physics and Astronomy
Depositing User: Giles Tarver
Date Deposited: 10 Jul 2015 15:21 UTC
Last Modified: 16 Nov 2021 10:20 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/49496 (The current URI for this page, for reference purposes)

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