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The new 4-amino-1,2,4-triazole asymmetric bridging ligand 4-amino-5-(pyridin-3-yl)-3-[4-(pyridin-4-yl)phen­yl]-4H-1,2,4-triazole (L) has been used to generate three novel isomorphic one-dimensional coordination polymers, viz. catena-poly[[tris­[dichloridomercury(II)]-bis­{[mu]3-4-amino-5-(pyridin-3-yl)-3-[4-(pyridin-4-yl)phen­yl]-4H-1,2,4-triazole}] aceto­nitrile monosolvate], {[Hg3Cl6(C18H14N6)2]·CH3CN}n, (I), and the bromido, {[Hg3Br6(C18H14N6)2]·CH3CN}n, (II), and iodido, {[Hg3I6(C18H14N6)2]·CH3CN}n, (III), analogs. The asymmetric ligand acts as a tridentate ligand to coordinate the three different HgII centers (two of which are symmetry-related). Two ligands and two symmetry-related HgII centers form centrosymmetric rectangular units which are linked into one-dimensional chains via the other unique Hg atoms, which sit on mirror planes. The chains are elaborated into a three-dimensional structure via inter­chain hydrogen bonds. The acetonitrile solvent mol­ecules are located in ellipsoidal cavities. The luminescent character of these three coordination complexes was investigated in the solid state.

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The new ether-bridged dipyridyl ligand 1,2-bis­[4-(pyridin-3-yl)phen­oxy]ethane (L) has been used to synthesize three isostructural centrosymmetric binuclear HgII macrocycles, namely bis­{μ-1,2-bis­[4-(pyridin-3-yl)phen­oxy]ethane-κ2N:N′}­bis­[dichloridomercury(II)], [Hg2Cl4(C24H20N2O2)2], and the bromido, [Hg2Br4(C24H20N2O2)2], and iodido, [Hg2I4(C24H20N2O2)2], analogues. The Hg atoms adopt a highly distorted tetra­hedral coordination environment consisting of two halides and two pyridine N-donor atoms from two bridging ligands. In the solid state, the macrocycles form two-dimensional sheets in the bc plane through noncovalent Hg...X and X...X (X = Cl, Br and I) inter­actions.
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