The unusual ( syn -/ anti -) 2 conformation of a di-meth-oxy-pyrimidyl-based tennimide.

The tennimide macrocycle, ( I ) (C 52 H 40 N 16 O 16 .0.167H 2 O), was synthesized from 2-amino-4,6-di-meth-oxy-pyrimidine and pyridine-2,6-dicarbonyl dichloride. Compound ( I ) represents the first tennimide incorporating pyridine rings in the macrocycle scaffold. In the macrocycle ring, the carbonyl groups at each successive dicarbon-yl(pyridine) moiety adopt the ( syn / anti ) 2 conformation. This contrasts with all previously reported tetra-imide macrocycles, which exhibit the ( syn ) 4 conformation. The effect is to close any potential cavity or niche by having two of the central pyridine C 5 N rings aligned close to each other [with closest pyridine Cg ⋯ Cg ring centroid separations of 3.5775 (19) Å; closest C⋯C = 3.467 (5) Å]. A partial occupancy water mol-ecule (with s.o.f. = 0.167), resides with its oxygen atom on a twofold axis at hydrogen-bonding distances to the carbonyl O atom, in a mol-ecular niche between two pyridine rings. Macrocyles of ( I ) have all six C=O groups and all eight meth-oxy O atoms present on the macrocycle surface. However, all twelve N atoms are effectively shielded on steric grounds from any potential inter-molecular inter-actions. The remaining two C=O O atoms inter-act with the partial occupancy water mol-ecule via two O-H⋯O=C hydrogen bonds. Macrocycles of ( I ) stack as one-dimensional chains along the b -axis direction with primary inter-molecular inter-actions involving weak C-H⋯O=C/OCH 3 /H 2 O contacts. Chains inter-lock weakly via meth-oxy-meth-oxy C-H⋯O inter-actions into two-dimensional sheets.