A 1st-generation oligomer (1) was designed to have a reduced diameter at each extremity and a wider diameter at the centre that includes a metal-coordinating site and was prepared following a well-established procedures.
The results obtained in solution by circular dichroism (CD) and NMR spectroscopies and in the solid state by X-ray crystal structure analysis showed that 1 can coordinate several metal ions leaving part of their coordination sphere available to bind a guest.
Interestingly Mg2+, Ca2+ and Ba2+ binding occurs through 2nd-coordination sphere interactions, i.e. through hydrogen bonds between the capsule inner wall and hydration sphere of the metals. This result expanded the scope of molecular recognition by aromatic helical foldamers.
The ability of the metal-containing sequence 1 to bind carbohydrate guests was assessed in solution using CD and NMR spectroscopies. The results showed that sequence 1 does not bind D-threitol, a 4-carbon carbohydrate, unless it is in the form of a metal complex. In addition, it was found that affinity towards this guest depends on the nature of the metal ion.
The crystal structure of 1-K+/threitol complex validated the complete encapsulation and the involvement of the metal ion in the direct coordination of the guest. The same was found in the case of the crystal structure of 1-Cu2+/threitol complex although here the guest is bound through 2nd-sphere coordination.
To be able to bind larger carbohydrate guests, a 2nd-generation foldamer (2) featuring a larger cavity size was designed and synthesized.
CD titrations showed that 2-Cu2+ can bind various monosaccharide guests in solution and revealed a preference for D-mannose over D-glucose, D-galactose and D-fructose.
An X-ray crystal structure showed that Cu2+ does not bind directly to the guest, but instead solvent molecules bridge the metal ion and the guest. The cavity was found to be too large to efficiently bind D-mannose, which occupies only 43% of the total cavity volume, which agrees with the moderate affinities found for the monosaccharide guests.
A fluorescent monomer was prepared and incorporated in a capsule sequence. Fluorescence spectroscopy titrations showed that an increase in guest concentration causes a decrease in fluorescence intensity, providing proof of concept that a fluorophore can be incorporated on to foldamer capsule sequences and serve as reporter of the binding event.
The results obtained gave rise to two publications in an international peer reviewed journal: Chem. Commun., 2017, 53, 9300 (Featured on inside front cover) and Chem. Commun., 2018, 54, 5078.
Moreover, the work has been presented on several occasions in international meetings: Symposium on Foldamers, Pessac, France, 2016; Conference on Functional Nanocontainers, Tarragona, Spain, 2016 and 12th International Symposium on Macrocyclic and Supramolecular Chemistry, Cambridge, UK, 2017.