Structural Variation and Supramolecular Isomerism in the C-Methylcalix[4]resorcinarene/Bipyridine System

摘要

Five supramolecular compounds [CMCR·3bipy] 2, [CMCR·2bipy·2H_2O] 3, [2CMCR]·1.5bipy·5H_2O_4, and [CMCR·bipy]·3.5ethanol·H_2O·bipy 5 (where the square brackets enclose framework components, CMCR = C-methylcalix[4]resorcinarene, bipy = 4,4'-bipyridine), prepared hydrothermally and from solution, are described. CMCR adopts a chair conformation in 1 and 2, and a flattened cone conformation in 3-5. The framework structures vary from 2D stepped-sheet (1), 3D stepped sheet (2), brick-wall (3 and 5) to a network consisting of perpendicular nonintersecting ribbons of CMCR molecules (4). The supramolecular architectures found in the current study are compared with those of other multicomponent CMCR/bipy system reported in the literature. The nature of the enclosed cavities in the brick-wall type structures is a function of the number of phenoxyl OH groups not involved in the framework hydrogen bonding, and thus available for bonding to guest molecules. The number of solvent-binding phenoxyl groups per CMCR ranges from two to zero in the brick-wall structures surveyed here.