Abstract

Cryptands, a class of three-dimensional macrobicyclic hosts ideally suited for accommodating small guest ions, have played an important role in the early development of supramolecular chemistry. In contrast to related two-dimensional crown ethers, cryptands have so far only found limited applications, owing in large part to their relatively inefficient multistep synthesis. We have recently described a convenient one-pot, template synthesis of cryptands based on O,O,O-orthoesters acting as bridgeheads. Here we report variable-temperature, 1H-1D EXSY and titration NMR studies on lithium, sodium, and potassium complexes of one such cryptand (o-Me2-1.1.1). Our results indicate that lithium and sodium ions fit into the central cavity of the cryptand, resulting in a comparably high binding affinity and slow exchange with the bulk. The potassium ion binds instead in an exo fashion, resulting in relatively weak binding, associated with fast exchange kinetics. Collectively, these results indicate that orthoester cryptands such as o-Me2-1.1.1 exhibit thermodynamic and kinetic properties in between those typically found for classical crown ethers and cryptands and that future efforts should be directed towards increasing the binding constants.

Highlights

  • Crown ethers [1,2] and cryptands [3,4,5,6] are iconic supramolecular hosts that through their interaction with small guest ions have contributed significantly to our current understanding of non-covalent interactions

  • Spectra indicative for slow cation exchange, whereas fast exchange was observed for the potassium complex. These results indicate at a qualitative level that the kinetics for the process of one metal ion hopping from one orthoester cage into another are significantly slower for lithium and sodium ions than for potassium ions

  • NMR spectroscopy we studied the kinetics of cation exchange at a quantitative level

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Summary

Introduction

Crown ethers (macrocyclic oligomers of ethylene glycol) [1,2] and cryptands (bicyclic structures made up of oligoethylene glycol arms and trialkylamine bridgeheads) [3,4,5,6] are iconic supramolecular hosts that through their interaction with small guest ions have contributed significantly to our current understanding of non-covalent interactions. Parsons and coworkers have synthesized related, yet less symmetric, macrobicycles in which two glycerol motifs act as bridgeheads [9,10,11]. Saalfrank and coworkers have self-assembled metallocryptates in which iron ions act as bridgeheads and a mix of nitrogen and oxygen donors is available for cation binding [12,13]

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