Knoevenagel condensation and cyanosilylation reactions catalyzed by a MOF containing coordinatively unsaturated Zn(II) centers

Abstract

An aqueous solution of Zn(NO₃)2·6H₂O reacts with tetraethylammonium salt of the tripodal ligand tris-(4-carboxy-2-phenoxyethyl)amine (ptaH₃) at room temperature, to form infinite interlinked 2D metallocycles. These 2D networks stack to form an overall 3D structure (1) where lattice water molecules occupy the metallocyclic cavities. On heating to 110 ° C for 5 h under vacuum, 1 loses metal bound water molecules as well as lattice ones without framework collapse and leaves the metal ion coordinatively unsaturated. The coordination space in the structure (1a) can be utilized for Knoevenagel and cyanosilation reactions to give biologically important molecules. These reactions are catalyzed by Zn(II) centers which are coordinatively unsaturated. Larger carbonyl substrates cannot diffuse through the pores of 1a, and afford poor yields of the desired products.