3-D Lanthanide Metal-Organic Frameworks: Structure, Photoluminescence, and Magnetism

Abstract

A series of isostructural three-dimensional metal-organic frameworks [Pr₂(N-BDC)₃(dmf)₄]_∞ (<b>1</b>), {[Eu₂(N-BDC)₃(dmf)₄]·2DMF}_∞ (<b>2</b>·2DMF), [Gd₂(N-BDC)₃(dmf)₄]_∞ (<b>3</b>), {[Tb₂(N-BDC)₃(dmf)₄]·2DMF}_∞ (<b>4</b>·2DMF), {[Dy₂(N-BDC)₃(dmf)₄]·2DMF}_∞ (<b>5</b>·2DMF) (N-H₂BDC = 2-amino-1,4-benzenedicarboxylic acid; DMF = N,N′-dimethylformamide) with cubic 4¹²·6³ topology have been synthesized using solvothermal conditions. The networks were generated via formation of a dinuclear Ln₂ secondary building block, involving the dicarboxylate ligand as a bridge. The luminescent properties of the Tb^III and Eu^III complexes were studied and showed characteristic emissions at room temperature. Antiferromagnetic interactions between Ln^III ions were observed from magnetic susceptibility data.