Two dichloride-bridged dinuclear dysprosium(III) complexes based on salen ligands, namely, [Dy(L 1 )(μ-Cl)(thf)] 2 (1; H 2 L 1 = N,N'-bis(3,5-di-tert-butylsalicylidene)phenylenediamine) and [Dy 2 (L 2 ) 2 (μ-Cl) 2 (thf) 2 ] 2 (2; H 2 L 2 = N,N'-bis(3,5-ditert-butylsalicylidene)ethylenediamine) are reported. These two complexes have two short DyÀ O (PhO) bonds that exhibit angles of ~90°for 1 and ~143°for 2, leading to clear slow relaxation of the magnetization for 2 and not for 1. Compound 2 has a near-identical core to the recently reported compound [Dy 2 (L 3 ) 2 (μ-Cl) 2 (thf) 2 ] (3; H 2 L 3 = N-(2pyridylmethyl)-N,N-bis(2'-hydroxy-3',5'-di-tertbutylbenzyl)amine). The only substantial difference is the relative angle of the two O (PhO) À DyÀ O (PhO) vectors, which is collinear in 2 owing to inversion symmetry and ~68°in 3 due to a molecular C 2 axis. It is shown that this subtle structural difference leads to large differences in the dipolar ground states, giving rise to open magnetic hysteresis for 3 and not for 2.