Specific Noncovalent Association of Truncated exo-Functionalized Triangular Homochiral Isotrianglimines through Head-to-Head, Tail-to-Tail, and Honeycomb Supramolecular Motifs.

ABSTRACT: Chiral isotrianglimines were synthesized by the [3 + 3] cyclocondensation of (R,R)-1,2-diaminocyclohexane with C5-substituted isophthalaldehyde derivatives. The substituent's steric and electronic demands and the guest molecules' nature have affected the conformation of individual macrocycles and their propensity to form supramolecular architectures. In the crystal, the formation of a honeycomb-like packing arrangement of the simplest isotrianglimine was promoted by the presence of toluene or para-xylene molecules. A less symmetrical solvent molecule might force this arrangement to change. Polar substituents present in the macrocycle skeleton have enforced the self-association of isotrianglimines in the form of tail-to-tail dimers. These dimers could be further arrange

SUBMITTER: Janiak A 

PROVIDER: S-EPMC8902749 | biostudies-literature | 2022 Mar

REPOSITORIES: biostudies-literature