This work centers around the nickel complexes derived from two tetrahydrosalen-type proligands: N,N'-bis(2-hydroxybenzyl)-o-phenylenediamine (H2salophan) and N,N'-bis(2-hydroxy-3-methylbenzyl)-o-phenylenediamine (H2salophan_Me). The reaction of H2salophan with Ni(OAc)2·4H2O generates a dinuclear complex Ni2(Hsalophan)2(OAc)2 or Na[Ni2(salophan)2(OAc)] when NaOH is added to assist ligand deprotonation. The reaction of H2salophan_Me with Ni(OAc)2·4H2O, however, yields a mononuclear complex Ni(Hsalophan_Me)2. Unlike the corresponding salen-type nickel complexes, these tetrahydrosalen-type complexes are paramagentic and air sensitive (in solution). Oxidation by O2 or peroxides results in dehydrogenation of the ligand backbone to form the salen-type complexes.