A series of nine new cadmium compounds of formal composition [Cd(m-X) 2 py 2 ] (X ~Cl, Br, I; py 3,5-disubstituted pyridine ligands with methyl, chloro, and bromo substituents) were synthesized and characterized by single crystal X-ray diffraction. Only for the combination of the sterically most demanding ligands, namely I and 3,5-dimethylpyridine, is a mononuclear tetrahedral complex obtained; in all other eight cases one-dimensional coordination polymers are found. In these chains cadmium(II) cations are linked in an edge-sharing fashion by halogen bridges in their pseudoequatorial plane, with terminal pyridine ligands completing the pseudo-octahedral coordination sphere. In all polymers the distance between neighboring Cd atoms corresponds to the shortest lattice constant: metal … metal separations systematically depend on both bridging and terminal ligands and range between 3.77 and 4.14 A ˚. This intermetal distance and the coordination mode of the donor ligands are found to be correlated. Five of the Cd chain polymers adopt the structure type found for [Zn(m-Cl) 2 py 2 ] ' . In addition to previous work the zinc derivatives [ZnX 2 (3,5-Me 2 py) 2 ] (X ~Cl, Br) were investigated for comparison and shown to be mononuclear.