Abstract
Control over the solubility properties of container molecules is a central challenge in host–guest chemistry. Herein we present a simple anion-exchange protocol that allows the dissolution in water of various hydrophobic metal–organic container molecules prepared by iron(II)-templated subcomponent self-assembly. Our process involved the exchange of less hydrophilic trifluoromethanesulfonate anions for hydrophilic sulfate; the resulting water-soluble cages could be rendered water-insoluble through reverse anion exchange. Notably, this strategy allowed cargoes within capsules, including polycyclic aromatic compounds and complex organic drugs, to be brought into water. Hydrophobic effects appeared to enhance binding, as many of these cargoes were not bound in non-aqueous media. Studies of the scope of this method revealed that cages containing tetratopic and tritopic ligands were more stable in water, whereas cages with ditopic ligands disassembled.
| Original language | English |
|---|---|
| Pages (from-to) | 9136-9140 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 56 |
| Issue number | 31 |
| DOIs | |
| Publication status | Published - 24 Jul 2017 |
Funding
This research was supported by the European Research Council (695009) and the UK Engineering and Physical Sciences Research Council (EPSRC, EP/M008258/1). We thank the Cambridge University Chemistry NMR facility for performing some NMR experiments and the EPSRC National Mass Spectrometry Facility at Swansea University for carrying out high-resolution analyses. E.G.P. acknowledges CONACyT Mexico for postdoctoral funding (263689). J.M. acknowledges postdoctoral fellowship support from Fundaci?n Ram?n Areces.
Keywords
- anion exchange
- host–guest systems
- self-assembly
- supramolecular chemistry
- water-soluble capsules
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