6533b835fe1ef96bd129f727

RESEARCH PRODUCT

Spin Crossover in Double Salts Containing Six- and Four-Coordinate Cobalt(II) Ions

Francesc LloretMiguel JulveBarbara MachuraNicolás MolinerJoanna Palion-gazdaThais GranchaRafal Kruszynski

subject

Pyrazine010405 organic chemistryLigandStereochemistryCationic polymerizationchemistry.chemical_element010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySpin crossoverPhysical and Theoretical ChemistryCobaltDicyanamide

description

The preparation and spectroscopic and structural characterization of three cobalt(II) complexes of formulas [Co(tppz)2](dca)2 (1), [Co(tppz)2][Co(NCS)4]·MeOH (2), and [Co(tppz)2][Co(NCO)4]·2H2O (3) [tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine and dca = dicyanamide] are reported here. Compounds 1–3 have in common the presence of the cationic [Co(tppz)2]2+ entity where each mer-tridentate tppz ligand coordinates to the cobalt(II) ion equatorially through two pyridyl donors and axially via the pyrazine, completing the six-coordination. The electroneutrality is achieved by the organic dca group (1) and the anionic tetrakis(thiocyanato-κN)cobaltate(II) (2) and tetrakis(cyanato-κN)cobaltate(II) (3) complexes. Direct current (dc) magnetic susceptibility measurements of 1 in the temperature range 1.9–400 K show the occurrence of a thermally induced spin crossover behavior of the [Co(tppz)2]2+ unit from a high spin (S = 3/2) at higher temperatures to a low-spin (S = 1/2) at lower temperatures, with the low spin pha...

https://doi.org/10.1021/acs.inorgchem.7b00360