Five polymeric metal(II)-benzoate complexes of formula [Mn(O2CPh)(2)(CH3OH)(2)(bpa)](n) (1-Mn), [Co(O2CPh)(2)(H2O)(bpa)(1.5)](n) (2-Co), [Ni(O2CPh)(2)(H2O)(bpa)(1.5)](n)(3-Ni), [Cu(O2CPh)(2)(CH3OH)(2)(bpa)](n) (4-Cu), and [Cd(O2CPh)(2)(bpa)(1.5)](n) (6-Cd) have been synthesized and characterized (bpa = 1,2-bis(4-pyridyl)ethane). They showed two kinds of structures: parallelogram-like two-dimensional sheets for Co, Ni, and Cd, and one-dimensional chains for Mn, Cu, and Zn. Since similar structures provide similar coordination geometries, the structures depend on the coordination geometries of metal ions. The compounds 1-Mn, 2-Co, 4-Cu, 5-Zn,and 6-Cd have catalyzed efficiently the transesterification of a variety of esters, while 3-Ni has displayed a very slow conversion. The reactivity of catalyst 6-Cd containing Cd ion, well known as an inert metal ion for the ligand substitution, was found to be comparable to that of 5-Zn. The reactivities of the compounds used in this study are in the order of 5-Zn > 6-Cd > 1-Mn > 4-Cu > 2-Co >> 3-Ni, indicating that the non-redox metal-containing compounds (5-Zn and 6-Cd) show better activity than the redox-active metal-containing compounds (1-Mn, 4-Cu, 2-Co, and 3-Ni). (C) 2009 Elsevier B.V. All rights reserved.