Abstract

A family of 3D lanthanide metal-organic frameworks, [La(HTADIP)(H(2)O)(4)]·xH(2)O (2 < x < 2.5) (1), [Eu(HTADIP)(H(2)O)(4)]·H(2)O (2), [Tb(HTADIP)(H(2)O)(3)]·2H(2)O (3), and [Er(HTADIP)(H(2)O)(3)]·2H(2)O (4) (H(4)TADIP = 5,5'-(1H-1,2,3-triazole-1,4-diyl)diisophthalic acid), have been hydrothermally synthesized and characterized. The unsymmetrical 1,2,3-triazole-containing tetracarboxylate ligand was synthesized through the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction of diethyl-5-azidoisophthalate (M1) and diethyl-5-ethynylisophthalate (M2). Single-crystal X-ray diffraction analyses for 1-4 reveal that they are isostructural. These compounds crystallize in the monoclinic P2(1)/c space group with the rutile topology. The luminescent properties of compounds 2 and 3 were investigated and characteristic Eu(III) and Tb(III) emissions are observed. Compound 3 exhibits selective luminescent sensing behavior for Cu(2+) ions in aqueous solution. The magnetic properties of compounds 3 and 4 were studied.

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