Abstract
Sulfonic acid groups with C3n symmetry can coordinate with metal ions to produce multidimensional structures due to their flexible coordination modes. They can also penetrate into supramolecular structures through an intriguing bridging pattern and weak interactions. Herein, a novel heterocyclic sodium sulfonate supramolecular structure, namely [Na(Pyr-SO3)(H2O)]n where Pyr-SO3H is pyrazine sulfonic acid, is synthesized by utilizing NaBF4 to coordinate with the P—SO3H ligand through the solvent evaporation method. The single crystal X-ray diffraction (XRD) data indicate that the as-formed structure belongs to the Pbca space group. Additional properties are characterized by powder XRD, thermal analysis, and solid-state fluorescence. In particular, the introduction of a soft alkali metal ion can coordinate with the oxygen atom of the sulfonate ligand and form a Na—O bridging configuration that can not only significantly improve the pyrazine sulfonic acid ligand coordination ability, but also provide a reference for the extended study of functional sulfonate polymers in the future.
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