Abstract

Hydrothermal reactions of Gd(III) nitrate with N, N, N′, N′-tetramethylenephosphono-1,4-diaminobutane, (H 2O 3PCH 2) 2N–(CH 2) 4–N(CH 2PO 3H 2) 2 (H 8L), afforded a novel Gd(III) phosphonate, namely, Gd[(O 3PCH 2)(HO 3PCH 2)N(H)(CH 2) 4N(H)(CH 2PO 3H) 2] · 2H 2O, [Gd(H 5L)] · 2H 2O. Its structure was established by a single-crystal X-ray diffraction study. In this compound, the Gd(III) ion is coordinated by eight phoshonate oxygen atoms from five different phosphonate groups, which belong to five different phosphonic ligands. Each Gd atom is connected with its neighboring Gd atoms by two phosphonate oxygens, forming a gadolinium phosphonate slab along the a-axis. Such slabs are bridged by tetraphosphonate H 5L anions, resulting in a 〈0 1 1〉 layer with the butane groups toward the interlayer space. These layers are further interlinked by strong hydrogen bonds formed by uncoordinated phosphonate oxygens into a 3D supermolecular structure. Luminescent studies indicate that this compound exhibits a broad blue fluorescent emission band at 441 nm.

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