Abstract
Dianiline-tetrapyridyloxy-cyclotriphosphazene (AnPyCp), as a novel flexible molecular building block, and its mercury(II) coordination polymers were successfully synthesized. The isolated crystalline coordination polymers, formulated as {[Hg(AnPyCp)(Cl)2]·CH3CN}n (1) and {[Hg2(AnPyCp)(I)4]·CH3CN}n (2), were structurally characterized by elemental analysis, FT-IR spectroscopy and single crystal X-ray crystallography. Furthermore, the X-ray crystal structure analysis revealed that complexes 1 and 2 crystallize in the triclinic crystal system with the P1¯ space group. In complexes 1 and 2, AnPyCp exhibited κ2N and κ3N coordination binding modes with the divalent Hg ions to form 1D chain structures. The central Hg2+ ion in complexes 1 and 2 has a distorted tetrahedral geometry. The UV–Vis properties and thermal stability of AnPyCp and its complexes (1 and 2) were also investigated. UV–Vis experiments, including titration and continuous variation (Job’s plot analysis), showed that all of the spectrophotometric properties in the solution state support the crystal structures of the complexes. According to TGA analysis, the coordination polymers exhibited thermal stability up to ∼230 °C, however AnPyCp showed a greater thermal stability than 1 and 2.
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