Abstract

The combination of 1,2-cyclohexanedionedioxime (NioxH2) and carboxylate-containing ligands resulted in Zn(II) or Cd(II) robust metal building blocks which being coupled with the flexible pyridine ligands fabricated five one-dimensional (1D) coordination polymers {[Cd(CHOO)2(NioxH2)(bpe)]·DMF}∞ (1), [Cd(CHOO)2(NioxH2)(dps)]∞ (2), [Zn(CH3COO)2(NioxH2)(dps)]∞ (3), [Cd(CH3COO)2(NioxH2)(dps)]∞ (4), and {[Zn(pyta)2(NioxH2)]·DMF}∞ (5) (where bpe = 4,4′-bipyridine ethane, dps = 4,4′-dipyridylsulfide, Hpyta = (4-pyridylthio)acetic acid, DMF = N,N-dimethylformamide), whose crystal structures were determined by single crystal X-ray diffraction. The stability of compounds 1 and 5 to loss of DMF as a guest has been addressed experimentally, and the crystal-to-crystal transformation observed for 1 resulted in the guest free 1D polymer [Cd(CHOO)2(NioxH2)(bpe)]∞ (1a) which maintains its coordination network with the 10.3% unit cell volume contraction, while compound 5 remains unchangeable under the same conditions. Compounds 1, 5 and the dioxime-free 1D polymer [Cd(pyta)2(H2O)]∞ (6) display blue luminescence upon excitation with ultraviolet light. The emission intensity of the guest-loaded complex 1 is effectively reduced in comparison with the previously reported DMF free analogues [Zn(CH3COO)2(NioxH2)(bpe)(H2O)]∞ and [Cd(CH3COO)2(bpe)(H2O)]∞.

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