Abstract
The assembly of hydrogen bonded cages using amidinium∙∙∙carboxylate hydrogen bonding interactions was
investigated. A new tris-amidinium hydrogen bond donor tecton based on a tetraphenylmethane scaffold was
prepared and its self–assembly with the terephthalate anion studied, and a new tricarboxylate hydrogen bond
acceptor tecton was synthesized and its assembly with the 1,3-benzenebis(amidinium) hydrogen bond donor
explored. In both cases, molecular modelling indicated that the formation of the cages was geometrically feasible
and 1H NMR spectroscopic evidence was consistent with interactions between the components in competitive d6-
DMSO solvent mixtures. DOSY NMR spectroscopy of both systems indicated that both components diffuse at the
same rate as each other, and diffusion coefficients were consistent with cage formation, and with the formation of
assemblies significantly larger than the individual components. An X-ray crystal structure showed that one of the
assemblies did not have the desired cage structure in the solid state
Supplementary materials
Title
Amidinium carboxylate cages SI
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Title
Amidinium carboxylate cages ToC
Description
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