Issue 16, 2013
From the journal:

CrystEngComm

Iodo-imidazolium salts: halogen bonding in crystals and anion-templated pseudorotaxanes†

Antonio Caballero,a   Sam Bennett,a   Christopher J. Serpellab  and  Paul D. Beer*a  

* Corresponding authors

a Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK
E-mail: paul.beer@chem.ox.ac.uk
Fax: +44 (0) 1865 272609

b Department of Chemistry, McGill University, Room 400, 801 Sherbrooke St. West, Montreal, Quebec, H3A 2K6, Canada
E-mail: christopher.serpell@mcgill.ca

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.

Graphical abstract: Iodo-imidazolium salts: halogen bonding in crystals and anion-templated pseudorotaxanes

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Article information

DOI
https://doi.org/10.1039/C2CE26020D
Article type
Communication
Submitted
26 ⵢⵓⵏ 2012
Accepted
25 ⵢⵓⵍ 2012
First published
13 ⵖⵓⵛ 2012

CrystEngComm, 2013,15, 3076-3081

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Iodo-imidazolium salts: halogen bonding in crystals and anion-templated pseudorotaxanes

A. Caballero, S. Bennett, C. J. Serpell and P. D. Beer, CrystEngComm, 2013, 15, 3076 DOI: 10.1039/C2CE26020D

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