| Abstract |
Solvothermal reactions between a pyridine based amide functionalized dicarboxylic acid, 4,4 -\(pyridine-2,6-dicarbonyl)bis(azanediyl)\dibenzoic acid (H2L), and zinc(II) nitrate in the absence and presence of a base produced the binuclear metallomacrocyclic compound [Zn-2(L)(2)(H2O)(4)]center dot 2(H2O)center dot 6(DMF) (1) and the metallomacrocyclic based two dimensional MOF [Zn-5(L)(4)(OH)(2)(H2O)(4)] n center dot 8n(DMF)center dot 4n(H2O) (2), respectively. Compound 1 bears two tetrahedral Zn(II) centres, whereas the 2D framework 2 includes a penta-nuclear Zn(II) cluster as a secondary building block unit, with two of the metal cations assuming a tetrahedral type geometry and the remaining three an octahedral type geometry. The topological analyses reveal that compound 1 has a 2-connected uninodal net and framework 2 has a 2, 8-connected binodal net. These compounds heterogeneously catalyse the tandem deacetalization-Knoevenagel condensation reactions carried out under conventional heating, microwave irradiation or ultrasonic irradiation. Comparative studies show that ultrasonic irradiation (final product yield of 99\% after 2 h of reaction time) provides the most favourable method (e.g., microwave irradiation leads to a final product yield of 91\% after 3 h of reaction time). Moreover, the catalysts can be reused at least for five consecutive cycles without losing activity significantly. |
