Abstract

Hydrothermal treatment of zinc chloride, 1,3,5-benzenetricarboxylic acid (H 3BTC), and 4,4′-dipyridylamine (dpa) afforded two different complexes depending on reaction conditions, which were characterized by single-crystal X-ray diffraction, infrared spectroscopy, and elemental analysis. Under acidic conditions, a discrete neutral molecular species with formulation [Zn(HBTC) 2(Hdpa) 2] ( 1) was isolated, which aggregates into two-dimensional hydrogen-bonded layers. Under more basic conditions, the two-dimensional layered coordination polymer [Zn(BTC)(Hdpa)] ( 2) is obtained, which manifests covalent linkage of [Zn(BTC)(Hdpa)] serpentine chain motifs into 3-connected undulating 4.8 2 topology 2-D layers. Both 1 and 2 possess tetrahedral coordination at Zn. Use of cadmium nitrate in the synthesis resulted in [Cd(BTC)(H 2O)(Hdpa)] ( 3), which displays a similar layer topology as 2 but with significant adjustments imparted by octahedral coordination at Cd. In all cases, supramolecular hydrogen bonding promoted by Hdpa ligands provide an important assistive structure-directing role. All materials display blue luminescence upon excitation with ultraviolet light, ascribed to intraligand transitions. Crystallographic data: 1: monoclinic, C2/ c, a=25.389(6) Å, b=9.811(2) Å, c=17.309(4) Å, and β=128.957(3)°, 2: monoclinic, P2 1/ c, a=13.212(17)c, b=17.15(2) Å, c=7.506(10) Å, and β=93.71(2)°, and 3: monoclinic, C2/ c, a=14.241(6) Å, b=15.218(6) Å, c=17.976(7) Å, and β=109.330(6)°.

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