Synthesis, Crystal Structure and Catalytic Behavior of Homo- and Heteronuclear Coordination Polymers [M(tdc)(bpy)] (M<sup>2+</sup> = Fe<sup>2+</sup>, Co<sup>2+</sup>, Zn<sup>2+</sup>, Cd<sup>2+</sup>; tdc<sup>2–</sup> = 2,5-thiophenedicarboxylate)

Abstract

A series of isostructural 3D coordination polymers <sup>3</sup><sub>∞</sub>[M­(tdc)­(bpy)] (M<sup>2+</sup> = Zn<sup>2+</sup>, Cd<sup>2+</sup>, Co<sup>2+</sup>, Fe<sup>2+</sup>; tdc<sup>2–</sup> = 2,5-thiophenedicarboxylate; bpy = 4,4′-bipyridine) was synthesized and characterized by X-ray diffraction, thermal analysis, and gas adsorption measurements. The materials show high thermal stability up to approximately 400 °C and a solvent induced phase transition. Single crystal X-ray structure determination was successfully performed for all compounds after the phase transition. In the zinc-based coordination polymer, various amounts of a second type of metal ions such as Co<sup>2+</sup> or Fe<sup>2+</sup> could be incorporated. Furthermore, the catalytic behavior of the homo- and heteronuclear 3D coordination polymers in an oxidation model reaction was investigated

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