Caballero, A., Bennett, S., Serpell, C.J., Beer, P.D. (2013) Iodo-imidazolium salts: Halogen bonding in crystals and anion-templated pseudorotaxanes. CrystEngComm, 15 (16). pp. 3076-3081. ISSN 14668033 (ISSN). (doi:10.1039/c2ce26020d) (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:49481)
| 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: http://www.scopus.com/inward/record.url?eid=2-s2.0... |
Abstract
The 2-iodoimidazolium group is exploited in the anion-templated assembly of pseudorotaxanes with isophthalamide containing macrocycles. Crystallographic and solution-phase studies illustrate that the iodo-imidazolium motif is a potent halogen bond donor, forming the most stable interpenetrated assemblies in solution with the chloride anion template. © 2013 The Royal Society of Chemistry.
| Item Type: | Article |
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| DOI/Identification number: | 10.1039/c2ce26020d |
| Additional information: | Unmapped bibliographic data: LA - English [Field not mapped to EPrints] J2 - Crystengcomm [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 - Department of Chemistry, McGill University, 801 Sherbrooke St. West, Montreal, QC H3A 2K6, Canada [Field not mapped to EPrints] DB - Scopus [Field not mapped to EPrints] |
| Subjects: | Q Science > QD Chemistry |
| Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
| Depositing User: | Giles Tarver |
| Date Deposited: | 10 Jul 2015 15:54 UTC |
| Last Modified: | 05 Nov 2024 10:34 UTC |
| Resource URI: | https://kar.kent.ac.uk/id/eprint/49481 (The current URI for this page, for reference purposes) |
University of Kent Author Information
Serpell, C.J..
| Creator's ORCID: |
 https://orcid.org/0000-0002-2848-9077
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