Abstract
Four new lanthanide–organic coordination polymers incorporating both nitrogen heterocyclic dicarboxylate and formate coligands, namely, {[Ln3(Heimda)4(μ2-HCOO)·4H2O]·2H2O}n, (Ln = Sm (1), Dy (2), Ho (3), Er (4), H3eimda = 1H-2-ethyl-4,5-imidazole-dicarboxylic acid) have been fabricated successfully and characterized systematically. The polymers 1–4 are isomorphous and isostructural, and are built from two dimensional (2-D) double decker networks based on the Ln4Heimda4 tetranuclear basic carboxylate as a secondary building unit (SBU). The extensive hydrogen bonds stabilize the crystal structure, forming a 3-D supramolecular tectonics. The luminescence emission spectra of the polymers vary depending on which lanthanide(III) ion is present. Variable-temperature magnetic susceptibility measurements show that the same end-to-end bridging fashion of formate results in the different magnetic properties occurring between adjacent lanthanide(III) centers.
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