Abstract

AbstractThe hydrothermal reaction of the tricarboxylate ligand 5‐(carboxymethoxy)isophthalic acid (H3L) with ZnII, CdII, and SnII salts in the presence of the bisbenzoimidazole coligand 1, 3‐bis(benzimidazol‐2‐yl)‐2‐oxapropane (bbop) afforded the coordination polymers, [Zn(HL)(bbop)]n (1), [Cd(HL)(bbop)]n (2), and {[H2(bbop)][Sn2L2]}n (3). The complexes were characterized by elemental analyses, IR spectroscopy, single‐crystal X‐ray diffraction analyses, thermogravimetric analyses, and fluorescence properties. The structures of complexes 1 and 2 are constructed by 1D chains and show strong blue luminescence emission. The structure of complex 3 is a 2D anionic dilayer, and shows a vase‐like porous structure occupied by the bulky [H2(bbop)]2+ cation, which is an uncommon structural feature in transition metal coordination polymers. The three complexes are further connected by hydrogen bonds to form 3D supramolecular architectures.

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