A family of oxygen coordinated dichlorido-bridged n-X-2-pyridone (1, n = 3, X = Cl; 2, n = 3, X = Br; 3, n = 4, X = Cl; 4, n = 4, X = Br; 5, n = 5, X = Cl; 6, n = 5, X = Br) Cu(II) offset stacked dimer compounds, denoted molecular spin stairs, have been prepared and analyzed by single-crystal X-ray diffraction (1–4), powder X-ray diffraction (1–6), and variable temperature magnetic susceptibility measurements (1–6). Ferromagnetism is dominant in all compounds with a weaker antiferromagnetic exchange present in 1–4. The ferromagnetic exchange correlates to increased twist angles which are defined by the extent of the tetrahedral distortion of the copper coordination sphere and the identity of the halogen on the ring. The compounds were qualitatively fit to a ferromagnetic Heisenberg chain model with a Curie-Weiss interchain correction. The general Hamiltonian used is of the form  H=−J∑S1S2. The ratio of exchange energies denoted α (α=JFM|JAFM|) ranges between 2.6 and 4.7. This family of compounds constitutes possible S = ½ Haldane-like materials.