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Superior anion induced shuttling behaviour exhibited by a halogen bonding two station rotaxane

DOI: 10.1039/C6SC00783J DOI Help

Authors: Timothy A. Barendt (University of Oxford) , Sean W. Robinson (University of Oxford) , Paul D. Beer (University of Oxford)
Co-authored by industrial partner: No

Type: Journal Paper
Journal: Chem. Sci.

State: Published (Approved)
Published: April 2016
Diamond Proposal Number(s): 9981

Abstract: Two bistable halogen and hydrogen bonding-naphthalene diimide [2]rotaxanes have been prepared and the system incorporating a halogen bond donor anion recognition site is demonstrated to exhibit superior anion induced translational motion of the macrocyclic wheel component relative to the hydrogen bonding analogue. Proton NMR spectroscopy is used to estimate the percentage occupancies of the macrocycle at the respective station and importantly indicates that the halogen bonding rotaxane displays superior positional integrity in competitive protic solvent media as a consequence of strong halogen bond–halide anion binding interactions

Subject Areas: Chemistry


Instruments: I19-Small Molecule Single Crystal Diffraction

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