Abstract
Individually prepared, equivalent amounts of 2,5-bis-(4-pyridyl)-1,3,4-oxadiazole (4-BPO) and benzenehexacarboxylic acid (mellitic
acid, MA) when mixed, deposited long rods, whose X-ray structure showed a unique assembly of 40 membered planar modules composed
from two alternating units each of MA and 4-BPO, rather than the anticipated helical profile. Several novel features of complexes
of MA with organic molecules are seen here. In almost all cases the intermolecular hydrogen bonding between MA anions is so
stable that the MA anions and the complementary cations lie in separate planes. This barrier is overcome in the present case.
The basic module associates to form quartets by very simple hydrogen bonding of the carboxylic groups of MA. The quartet assembly
is characterized by the rotation of the left hand pair compared to the right hand pair. The mode of the macromolecular assembly
is clear, that is, they are layered in alternating planes. Space group: P21/c with a = 9.181(1) Å, b = 9.624(1) Å, c = 29.390(2) Å, and β = 94.626(4)°. The modules are embedded in an extensively hydrogen bonded MA network. The assembly profile of MA and 4-BPO
is unique and should be a harbinger for the design of novel functional assemblies. The 40-membered module mimics the self-assemblies
of peptides and can be important in the design of “Haptens” from simple molecules.
Index Abstract
Rod like crystals from water that are formed on mixing MA and 4-BPO are shown to consist of 4-molecule modules (MA–4-BPO–MA–4-BPO–)
that contain a 40-membered ring, MA–BPO.
Keywords Macrocyclic module (40) - Non-covalent self-assembly - Modules to supramolecules