Nickel(II) complexes with tetradentate N4 ligands: Synthesis, structure, electrochemistry and thermochromism in solution

Complexes of nickel(II) chloride with homologous tetradentate aminopyridine ligands 1,8-bis(2-pyridyl)-3,6-dimethyl-3,6-diazaoctane (pdao) and 1,6-bis(2-pyridyl)-2,5-dimethyl-2,5-diazahexane (bpmen) were prepared in the crystalline state and characterized by elemental analysis and X-ray diffraction as [Ni(pdao)(H2O)2]Cl2·H2O (1) and [Ni(bpmen)Cl2]·H2O (2). In the solid state, both complexes are blue-green and contain octahedral Ni(II) with a cis-α-coordinated tetramine. In aqueous solution, both complexes are strong electrolytes as follows from the measurements of electrical conductivity: complex 2 is hydrated and forms purple [Ni(bpmen)(H2O)2]2+(aq). Complex 1 displays thermochromic behavior in solution (it is blue-green at low temperatures and yellow at high temperatures) due to a temperature sensitive equilibrium [Ni(pdao)(H2O)2]2+(aq) ⇄ [Ni(pdao)]2+(aq) + 2H2O(l), ΔH° = +30(1) kJ/mol and ΔS° = +80(3) J/mol K in 0.1 M NaClO4(aq). Complex 1, but not 2, can be reversibly reduced to the Ni(I) species (E1/2 = −0.9 V versus SHE in aqueous solution and −1.37 V versus Fc+/Fc in acetonitrile). The relative stabilization of nickel(I) by ligand pdao can be attributed to an optimal size of the ligand bite and to the presence of the pyridine and tertiary amine N-donors.