CoIIComplexes with a Tripyridine Ligand, Containing a 2,6-Di-tert-butylphenolic Fragment: Synthesis, Structure, and Formation of Stable Radicals

Abstract

Interaction of a tripyridine ligand bearing a 2,6-di-tert-butylphenolic fragment (L, 2,6-di-tert-butyl-4-(3,5-bis(4-pyridyl)pyridyl)phenol) with CoII pivalate or chloride led to the formation of one-dimensional coordination polymers [Co(L)Cl2]n·nEtOH (1) and [Co3(L)2(OH)(Piv)5]n (2) or a trinuclear complex Co3(H2O)4(L)2Cl6 (3) (Piv– = pivalate). Chemical oxidation of L and 1–3 by PbO2 or K3[Fe(CN)6], as well as exposure of L (in solution or solid state) and 2 (in solid state) to UV irradiation, led to the formation of free radicals with g = 2.0024, which probably originated because of oxidation of 2,6-di-tert-butylphenolic groups. These radicals were stable for several days in solutions and more than 1 month in solid samples. Irradiation and oxidation of the solid samples probably caused formation of the phenoxyl radical only on their surface. It was shown by density functional theory calculations that exchange coupling between the unpaired electron of the phenoxyl radical and CoII ions was negligibly weak and could not affect the electron paramagnetic resonance signal of the radical, as well as exchange coupling of CoII ions could not be transmitted by L. The latter conclusion was confirmed by the analysis of magnetic properties of 1: temperature dependency of magnetic susceptibility (χM) of 1 could be simulated by a simple model for isolated CoII ions.