A range of secondary dialkylammonium (R2NH2+) ions has been shown to thread
through the cavities of appropriately-sized crown ether compounds to affor
d interwoven complexes. X-Ray crystallographic investigations to probe the
solid-state properties of these supermolecules have revealed that many subt
le factors-e.g., solvent of crystallisation, crown ether conformation and a
nion interactions-can influence the nature of the overall three-dimensional
superstructures. Nonetheless, a family of building blocks-namely R2NH2+ io
ns and crown ethers-can be generated, which constitute a molecular meccano
kit. By mixing and matching these modules in different ways, intricate inte
rwoven supramolecular architectures can be constructed. From relatively sim
ple beginnings-where one R2NH2+ ion is threaded through one monotopic crown
ether (dibenzo[24]crown-8)-the designed evolution of the building blocks i
n the molecular meccano kit has led to more elaborate multiply encircled an
d/or multiply threaded superstructures. The effects of crown ether constitu
tion, macroring size, and both crown ether as well as R2NH2+ ion substituti
on, upon the solid-state behaviour of these interwoven complexes have also
been examined. A statistical analysis of the hydrogen bonding interactions
observed in these systems has been carried out. It reveals that a reasonabl
e correlation exists between N+-H . . .O bond angle and H . . .O bond lengt
h. The correlation between C-H . . .O bond angle and H . . .O distance is p
oor, suggesting that C-H . . .O hydrogen bonding interactions are of second
ary importance in determining the co-conformations adopted by these supermo
lecules.