Two new copper(II) complexes, [Cu 2 (3-bpfp)(2,6-PDA) 2 (H 2 O) 2 ] (1) and 0.5 (glu)]·H 2 O (2), have been hydrothermally synthesized by self-assembly of isomeric bis(pyridylformyl)piperazine ligands [3-bpfp = bis(3-pyridylformyl)piperazine, 4-bpfp = bis(4-pyridylformyl)piperazine], rigid pyridine-2,6-dicarboxylic acid (2,6-H 2 PDA) or flexible glutaric acid (H 2 glu), and copper(II) chloride. Single-crystal X-ray diffraction analysis reveals that two adjacent Cu II ions are connected by the 3-bpfp ligand to build a dinuclear unit in complex 1, in which 2,6-PDA serves as a terminal chelating ligand. Adjacent dinuclear units are further linked by hydrogen bonding and π-π stacking interactions to form a three-dimensional (3D) supramolecular network. Complex 2 is a 3D coordination polymeric framework based on a layer polymer [Cu(glu)] n and bridging 4-bpfp ligands with 6-connected (4 4 .6 10 .8) topology. In 1 and 2, the ligands 3-bpfp and 4-bpfp adopt a µ 2 -bridging coordination mode (via ligation of pyridyl nitrogen atoms). The thermal stability and the electrochemical properties of the title complexes have been studied.