Understanding the Stabilization and Tunability of Divalent Europium 2.2.2B Cryptates

Abstract

Lanthanides such as europium with more accessible divalent states are useful for studying redox stability afforded by macrocyclic organic ligands. Substituted cryptands, such as 2.2.2B cryptand, that increase the oxidative stability of divalent europium also provide coordination environments that support synthetic alterations of Eu(II) cryptate complexes. Two single crystal structures were obtained containing nine-coordinate Eu(II) 2.2.2B cryptate complexes that differ by a single coordination site, the occupation of which is dictated by changes in reaction conditions. A crystal structure containing a [Eu(2.2.2B)Cl]⁺ complex is obtained from a methanol-THF solvent mixture, while a methanol-acetonitrile solvent mixture affords a [Eu(2.2.2B)(CH₃OH)]²⁺ complex. While both crystals exhibit the typical blue emission observed in most Eu(II) containing compounds as a result of 4f⁶5d¹ to 4f⁷ transitions, computational results show that the substitution of a Cl^- anion in the place of a methanol molecule causes mixing of the 5d excited states in the Eu(II) 2.2.2B cryptate complex. Additionally, magnetism studies reveal the identity of the capping ligand in the Eu(II) 2.2.2B cryptate complex may also lead to exchange between Eu(II) metal centers facilitated by π-stacking interactions within the structure, slightly altering the anticipated magnetic moment. The synthetic control present in these systems makes them interesting candidates for studying less stable divalent lanthanides and the effects of precise modifications of the electronic structures of low valent lanthanide elements.