Abstract

This paper presents the hydrothermal synthesis of a series of new isomorphous bis-dipicolinato lanthanide complexes: Ln(Hdipic)(dipic) with Ln=Eu, Gd, Tb, Dy, Ho, Er, Yb, and dipic=2,6-pyridinedicarboxylate. A structural study has been realised for the Ho 3+ complex. It crystallises in a two-dimensional network, where sheets are parallel to the (100) plane. The luminescent properties of the analogous Eu 3+ complex have been investigated. The composition of the 7F J levels is consistent with a true C 1 local symmetry: six oxygen and two nitrogen atoms forming a distorted square antiprism. The 5D 0 emission lifetime is only slightly shorter than in [Eu(dipic) 3] 3− in solution, but the ligand to metal energy transfer is much less efficient.

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