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Halotriazolium axle functionalised [2]rotaxanes for anion recognition: Investigating the effects of halogen-bond donor and preorganisation

Halotriazolium axle functionalised [2]rotaxanes for anion recognition: Investigating the effects of halogen-bond donor and preorganisation
Halotriazolium axle functionalised [2]rotaxanes for anion recognition: Investigating the effects of halogen-bond donor and preorganisation
The anion-templated synthesis of three novel halogen-bonding 5-halo-1,2,3-triazolium axle containing [2]rotaxanes is described, and the effects of altering the nature of the halogen-bond donor atom together with the degree of inter-component preorganisation on the anion-recognition properties of the interlocked host investigated. The ability of the bromotriazolium motif to direct the halide-anion-templated assembly of interpenetrated [2]pseudorotaxanes was studied initially; bromide was found to be the most effective template. As a consequence, bromide anion templation was used to synthesise the first bromotriazolium axle containing [2]rotaxane, the anion-binding properties of which, determined by 1HNMR spectroscopic titration experiments, revealed enhanced bromide and iodide recognition relative to a hydrogen-bonding protic triazolium rotaxane analogue. Two halogen-bonding [2]rotaxanes with bromo- and iodotriazolium motifs integrated into shortened axles designed to increase inter-component preorganisation were also synthesised. Anion 1HNMR spectroscopic titration experiments demonstrated that these rotaxanes were able to bind halide anions even more strongly, with the iodotriazolium axle integrated rotaxane capable of recognising halides in aqueous solvent media. Importantly, these observations suggest that a halogen-bonding interlocked host binding domain, in combination with increased inter-component preorganisation, are requisite design features for a potent anion receptor. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
anions, click chemistry, halogen bonding, host-guest systems, rotaxanes, supramolecular chemistry
0947-6539
11740-11749
Mercurio, James M.
7b7bdc7f-e98a-49db-8ef8-86b2074117f7
Knighton, Richard C.
5a63128e-0ebd-466a-b327-3aee6e85a76d
Cookson, James
413589e0-2738-4d68-afde-7b0f061901ef
Beer, Paul D.
6af15407-244d-4e11-8147-a62a04672f4e
Mercurio, James M.
7b7bdc7f-e98a-49db-8ef8-86b2074117f7
Knighton, Richard C.
5a63128e-0ebd-466a-b327-3aee6e85a76d
Cookson, James
413589e0-2738-4d68-afde-7b0f061901ef
Beer, Paul D.
6af15407-244d-4e11-8147-a62a04672f4e

Mercurio, James M., Knighton, Richard C., Cookson, James and Beer, Paul D. (2014) Halotriazolium axle functionalised [2]rotaxanes for anion recognition: Investigating the effects of halogen-bond donor and preorganisation. Chemistry - A European Journal, 20 (37), 11740-11749. (doi:10.1002/chem.201403317).

Record type: Article

Abstract

The anion-templated synthesis of three novel halogen-bonding 5-halo-1,2,3-triazolium axle containing [2]rotaxanes is described, and the effects of altering the nature of the halogen-bond donor atom together with the degree of inter-component preorganisation on the anion-recognition properties of the interlocked host investigated. The ability of the bromotriazolium motif to direct the halide-anion-templated assembly of interpenetrated [2]pseudorotaxanes was studied initially; bromide was found to be the most effective template. As a consequence, bromide anion templation was used to synthesise the first bromotriazolium axle containing [2]rotaxane, the anion-binding properties of which, determined by 1HNMR spectroscopic titration experiments, revealed enhanced bromide and iodide recognition relative to a hydrogen-bonding protic triazolium rotaxane analogue. Two halogen-bonding [2]rotaxanes with bromo- and iodotriazolium motifs integrated into shortened axles designed to increase inter-component preorganisation were also synthesised. Anion 1HNMR spectroscopic titration experiments demonstrated that these rotaxanes were able to bind halide anions even more strongly, with the iodotriazolium axle integrated rotaxane capable of recognising halides in aqueous solvent media. Importantly, these observations suggest that a halogen-bonding interlocked host binding domain, in combination with increased inter-component preorganisation, are requisite design features for a potent anion receptor. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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More information

Published date: 8 September 2014
Keywords: anions, click chemistry, halogen bonding, host-guest systems, rotaxanes, supramolecular chemistry

Identifiers

Local EPrints ID: 482000
URI: http://eprints.soton.ac.uk/id/eprint/482000
ISSN: 0947-6539
PURE UUID: 9d34855c-9a08-4415-a250-baeed92397ca
ORCID for Richard C. Knighton: ORCID iD orcid.org/0000-0002-0336-3718

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Date deposited: 14 Sep 2023 16:53
Last modified: 18 Mar 2024 04:15

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Contributors

Author: James M. Mercurio
Author: Richard C. Knighton ORCID iD
Author: James Cookson
Author: Paul D. Beer

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