Dimerization of Paramagnetic Trinuclear Complexes by Coordination Geometry Changes Showing Mixed Valency and Significant Antiferromagnetic Coupling through -Pt···Pt- Bonds.

Abstract

Paramagnetic trinuclear complexes, trans-[Pt2M(piam)4(NH3)4](ClO4)x (t-M; piam = pivalamidate, M = Mn, Fe, Co, Ni, and Cu, x = 2 or 3), aligned as Pt-M-Pt were successfully synthesized and characterized. The dihedral angles between the Pt and M coordination planes in t-M are approximately parallel, showing straight metal-metal bonds with distances of approximately 2.6 Å. Except for t-Fe, the trinuclear complexes are dimerized with close contact (approximately 3.9 Å) between the end Pt atoms to form Pt-M-Pt···Pt-M-Pt alignments with high-spin M(+2) containing five (t-Mn), three (t-Co), two (t-Ni), and one (t-Cu) unpaired electrons localized on M atoms. Several physical measurements and calculations revealed that the dimerized structures were maintained in MeCN, where cyclic voltammograms for t-M exhibited two-step oxidation and reduction attributed to Pt-M(+2)-Pt···Pt-M(+2)-Pt ↔ Pt-M(+3)-Pt···Pt-M(+2)-Pt ↔ Pt-M(+3)-Pt···Pt-M(+3)-Pt via mixed-valent states. Magnetic susceptibility measurements for t-M showed antiferromagnetic interaction, t-Mn: J = -0.9 cm-1, t-Co: J = -3.5 cm-1, t-Ni: J = -7.3 cm-1, and t-Cu: J = 0.0 cm-1, between the two M centers with distances of 9.0 Å through Pt···Pt bonds.