摘要:
                                This work presents a series of Zn-II, Cd-II, Co-II, and Pb-II supramolecular complexes assembled from a bent dipyridyl derivative 2,5-bis(3-pyridyl)-1,3,4-oxadiazole (3-bpo) and different dicarboxyl co-ligands 2-bromoterephthalic acid (H(2)BTA) and tetrabromoterephthalic acid (H(2)TBTA). All products have been prepared under similar conditions and characterized by IR, microanalysis, and TG-DTA techniques. Single-crystal X-ray diffraction indicates that these complexes display mononuclear, 1-D, and 2-D coordination motifs, and diverse higher-dimensional extended networks are further constructed via additional secondary interactions such as H-bonding and aromatic stacking. Notably, in situ hydrolysis reaction of 3-bpo is observed in the Pb-II complex with H(2)TBTA, affording another dipyridyl-type ligand N,N'-bis(3-picolinoyl)hydrazine (3-bph). These results evidently reveal the significant substituent effect of terephthalic acid in structural direction of these metallosupramolecular that are also regulated by the selection of metal ions. (C) 2009 Elsevier Ltd. All rights reserved.