Sulfonate···Pyridinium Supramolecular Synthon: A Robust Interaction Utilized to Design Molecular Assemblies

Abstract

An approach for supramolecular design through a sulfonate··· pyridinium synthon has been adopted to achieve the structural modulations in molecular complexes of metanilic acid and various pyridyl derivatives. Layered ionic solids [(3-ABSA)2–(4,4′-BPY-H)2+(4,4′-BPY)] (1) and [(3-ABSA)−(4,4′-BPP-H)+] (2) have been obtained by reacting metanilic acid (3-ABSA-H) with linear bis-4-pyridines: 4,4′-bipyridine (4,4′-BPY) and 4,4′-trimethylenedipyridine (4,4′-BPP). 1a, a polymorph of 1, obtained with a slight excess of metanilic acid, also exhibits the layered ionic structure. The tendency of bis-4-pyridines to form infinite N+–H···N assisted chains and hence layered structures is also supported by the literature. Attempts to break down the layered structures by employing nonlinear bis-pyridines, 2,2′-bipyridine (2,2′-BPY) and 1,7-phenanthroline (1,7-phen), lead to the isolation of [(3-ABSA)−(2,2′-BPY-H)+·H2O]2 (3) and [(3-ABSA)−(1,7-Phen-H)+(1,7-Phen)·H2O] (4). Compound 3 displays two-dimensional (2-D) framework structure with bis-pyridinium cations stacked in rectangular cavities, while in 4 one-dimensional (1-D) trilayer chains associate to form 2-D sheets, which in turn undergo π-interlocking to form a 3-D supramolecule. Monopyridyl derivative 4-phenylpyridine (4-PhPy) yields a pseudo-honeycomb framework [(3-ABSA)−(4-PhPy-H)+·H2O] (5), with pyridinium cations occupying the hives. [(1,5-DNSA)2–(4,4′-BPP-2H)2+·2H2O] (6), obtained with bis-sulfonic acid (1,5-DNSA-2H) and linear bis-pyridine, is a 2-D porous solid with water-associated bis-pyridinium chains bridged by bis-sulfonates through a masked sulfonate···pyridinium synthon. Interestingly, the supramolecular synthon manifests itself variedly: ionic interaction in 1, 1a, and 2; charge assisted hydrogen bonding interaction in 4 and 5; and water-masked interaction in 3 and 6. Enhanced thermal and chemical stability in molecular salts 1–6 may be attributed to proton transfer. Incipience of mild to intense color in 1–5 is attributed to extended π-stacking of pyridyl ligands. The products are also characterized by spectroscopic and thermogravimetric methods.