Abstract

A new bent 1,2,4-triazole-bridged N,N'-dioxide ligand, namely, 3,5-bis(3-pyridyl-N-oxide)-4-amino-1,2,4-triazole (L2), was designed and synthesized by the oxidation of 3,5-bis(3-pyridyl)-4-amino-1,2,4-triazole with H(2)O(2) in the presence of HOAc at ambient temperatures. Eleven Ln(III)-based coordination polymers have been successfully prepared by the solution reactions of L2 with various Ln(III)-perchlorates. The structures of these new Ln(III) polymers clearly reflect the effect of the lanthanide contraction. Compounds 1-6 feature a two-dimensional net, in which the Ln(III) atoms adopt a nine-coordinate {LnO(9)} sphere due to their larger ionic radii, whereas the Ln(III) centers in the one-dimensional double-stranded chains of 7-11 with smaller ionic radii lie in a {LnO(8)} coordination environment. In addition, the tunable emission intensity was realized on 7 by controlling the type of the involved counterion on the basis of a reversible solid-state anion exchange. Such reversible solid-state anion exchange might provide an alternative approach to tuning the luminescence.

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