Tuning of spin crossover properties in a series of mononuclear cobalt(II) complexes based on a macrocyclic tetradentate ligand and pseudohalide coligands.

The three mononuclear cobalt(II) complexes, [Co(L)(NCX)] (L = ,'-di--butyl-2,11-diaza3,3pyridinophane, and X = S (1), Se (2), and [C(CN)] (3)), have been synthesized and characterized using variable temperature single-crystal X-ray crystallography, and spectroscopic, magnetic, and electrochemical studies. All three complexes have a similar distorted octahedral CoN coordination geometry produced by the macrocyclic tetradentate ligand L and two NCX co-ligands in the position. Complexes 1 and 2 crystallized in the monoclinic 2/ ( = 4) space group, while complex 3 was isolated in the monoclinic 2/ ( = 4) space group. Interestingly, complexes 1 and 2 exhibit a reversible and gradual spin-crossover behavior between the high-spin ( = 3/2) and low-spin ( = 1/2) states at 168 K and 255 K, respectively. However, for complex 3, a low-spin configuration persists up to 260 K and it exhibits an incomplete and reversible spin crossover even at 400 K. In addition, complex 1 displays a reversible redox behavior indicating the paramagnetic cobalt(II) to diamagnetic cobalt(III) conversion.