Issue 19, 2002
From the journal:

Chemical Communications

Dual-mode recognition of oxalate by protonated azacryptate hosts; conformational response of the guest maximizes π-stacking interactions

Jane Nelson,*a   Mark Nieuwenhuyzen,b   Ibolya Pálb  and  Raewyn M. Townb  

* Corresponding authors

a School of Biomedical Sciences, University of Ulster, Coleraine, Northern Ireland, UK
E-mail: J.Nelson@ulst.ac.uk

b School of Chemistry, Queen’s University of Belfast, Belfast, Northern Ireland, UK

Abstract

Exceptionally large complexation constants for oxalate encapsulated within azacryptand hosts are partly explained by π-stacking interactions between C[double bond, length as m-dash]O and aromatic rings.

Graphical abstract: Dual-mode recognition of oxalate by protonated azacryptate hosts; conformational response of the guest maximizes π-stacking interactions

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Article information

DOI
https://doi.org/10.1039/B207964J
Article type
Communication
Submitted
14 Aug 2002
Accepted
28 Aug 2002
First published
12 Sep 2002

Chem. Commun., 2002, 2266-2267

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Dual-mode recognition of oxalate by protonated azacryptate hosts; conformational response of the guest maximizes π-stacking interactions

J. Nelson, M. Nieuwenhuyzen, I. Pál and R. M. Town, Chem. Commun., 2002, 2266 DOI: 10.1039/B207964J

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