Poly[di-μ(3)-hy-droxy[μ(4)-5-(4-carb-oxy-phen-yl)pyridine-2-carboxyl-ato-κ(5)N,O(2):O(2'):O(4):O(4')]dicadmium].

The asymmetric unit of the title polymeric complex, [Cd(2)(C(13)H(7)NO(4))(OH)(2)](n), consists of two independent Cd(II) atoms, one 5-(4-carb-oxy-phen-yl)pyridine-2-carboxyl-ate ligand and two hy-droxy groups. One Cd(II) atom is six-coordinated by two O atoms from two ligand mol-ecules and by four μ(3)-OH groups in a distorted trigonal-prismatic geometry. The other is five-coordinated by one N and two O atoms from two ligands and by two μ(3)-OH groups, forming a distorted square-pyramidal geometry.

Constructing mixed-metal coordination polymers from copper(II)-pyridinedicarboxylate metalloligands.

In the mixed-metal complex catena-poly[bis[diaquasilver(I)] [bis[aquacopper(II)]-mu(3)-pyridine-2,5-dicarboxylato-2':1:1'kappa(5)N,O(2):O(5):O(5),O(5')-mu-pyridine-2,5-dicarboxylato-2:1kappa(4)N,O(2):O(5),O(5')-disilver(I)-mu(3)-pyridine-2,5-dicarboxylato-1:1':2''kappa(5)O(5),O(5'):O(5):N,O(2)-mu-pyridine-2,5-dicarboxylato-1':2'''kappa(4)O(5),O(5'):N,O(2)] hexahydrate], {[Ag(H(2)O)(2)][AgCu(C(7)H(3)NO(4))(2)(H(2)O)].3H(2)O}(n), a square-pyramidal Cu(II) center is coordinated by two N atoms and two O atoms from two pyridine-2,5-dicarboxylate (2,5-pydc) ligands and a water molecule, forming a [Cu(2,5-pydc)(2)(H(2)O)](2-) metalloligand. One Ag(I) center is coordinated by five O atoms from three 2,5-pydc ligands and, as a result, the [Cu(2,5-pydc)(2)(H(2)O)](2-) metalloligands act as linkers in a unique mu(3)-mode connecting Ag(I) centers into a one-dimensional anionic double chain along the [101] direction.

catena-Poly[diammonium [diaqua-bis(pyridine-2,4-dicarboxyl-ato-κN,O)cuprate(II)] [[diaqua-copper(II)]-μ-pyridine-2,4-dicarboxyl-ato-κN,O:O-[tetra-aqua-cadmium(II)]-μ-pyridine-2,4-dicarboxyl-ato-κO:N,O] hexa-hydrate].

The title mixed-metal complex, {(NH(4))(2)[Cu(C(7)H(3)NO(4))(2)(H(2)O)(2)][CdCu(C(7)H(3)NO(4))(2)(H(2)O)(6)]·6H(2)O}(n), contains one octa-hedrally coordinated Cd(II) center and two octa-hedrally coordinated Cu(II) centers, each lying on an inversion center. The two Cu(II) atoms are each coordinated by two O atoms and two N atoms from two 2,4-pydc (2,4-H(2)pydc = pyridine-2,4-dicarboxylic acid) ligands in the equatorial plane and two water mol-ecules at the axial sites, thus producing two crystallographically independent [Cu(2,4-pydc)(2)(H(2)O)(2)](2-) metalloligands. One metalloligand exists as a discrete anion and the other connects the Cd(H(2)O)(4) units, forming a neutral chain.

Assembly of the highest connectivity Wells-Dawson polyoxometalate coordination polymer: the use of organic ligand flexibility.

Through tuning the length of flexible bis(triazole) ligands and different metal ion coordination geometries, four Wells-Dawson polyoxoanion-based hybrid compounds, [Cu 6(btp) 3(P 2W 18O 62)].3H 2O ( 1) (btp = 1,3-bis(1,2,4-triazol-1-y1)propane), [Cu 6(btb) 3((P 2W 18O 62)].2H 2O ( 2), [Cu 3(btb) 6(P 2W 18O 62)].

High-dimensional assembly depending on polyoxoanion templates, metal ion coordination geometries, and a flexible bis(imidazole) ligand.

By introducing the flexible 1,1'-(1,4-butanediyl)bis(imidazole) (bbi) ligand into the polyoxovanadate system, five novel polyoxoanion-templated architectures based on [As(8)V(14)O(42)](4-) and [V(16)O(38)Cl](6-) building blocks were obtained: [M(bbi)(2)](2)[As(8)V(14)O(42)(H(2)O)] [M = Co (1), Ni (2), and Zn (3)], [Cu(bbi)](4)[As(8)V(14)O(42)(H(2)O)] (4), and [Cu(bbi)](6)[V(16)O(38)Cl] (5). Compounds 1-3 are isostructural, and they exhibit a binodal (4,6)-connected 2D structure with Schläfli symbol (3(4) x 4(2))(3(4) x 4(4) x 5(4) x 6(3))(2), in which the polyoxoanion induces a closed four-membered circuit of M(4)(bbi)(4). Compound 4 exhibits an interesting 3D framework constructed from tetradentate [As(8)V(14)O(42)](4-) cluster anions and cationic ladderlike double chains.

Poly[di-mu3-chloro-mu2-trans-1,2-di-4-pyridylethylene-dicopper(I)]: a two-dimensional organic-inorganic hybrid constructed from linear CuCl clusters and bridging ligands.

The structure of the title compound, [Cu2Cl2(C12H10N2)](n), contains infinite CuCl staircase-like chains, which lie about inversion centres. The trans-1,2-di-4-pyridylethylene molecules also lie about inversion centres and connect the CuCl chains through Cu-N coordination bonds into a two-dimensional organic-inorganic hybrid network. The planar sheets are stacked along the c axis and associated through weak C-H.

Interactions of thiamine with polymeric halogenocadmate anions in the organic-inorganic hybrid compound (thiaminium)[Cd3Br4.4Cl3.6].

The structure of poly[3-[(4-amino-2-methylpyrimidin-1-ium-5-yl)methyl]-5-(2-hydroxyethyl)-4-methylthiazolium octa-mu-bromo/chloro(4.4/3.6)-tricadmate(II)], [(C12H18N4OS)[Cd3 Br4.

Thiamine tetraphenylborate monohydrate: a two-dimensional hydrogen-bonded network with (4,4)-topology.

The title compound, 3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-5-(2-hydroxyethyl)-4-methylthiazolium tetraphenylborate monohydrate, C12H17N4OS+.C24H20B-.H2O, is a salt in which the thiamine cations are linked by hydrogen bonds into a two-dimensional network having (4,4)-topology.

Synthesis and characterization of binuclear molybdenum-polycarboxylate complexes with sulfur bridges.

A group of four binuclear sulfur-bridged molybdenum-polycarboxylato complexes with homocitrate, citrate, cysteine, ethylenediaminetetraacetate ligands, respectively, have been synthesized and characterized. These complexes were prepared in order to study the interaction of Mo and homocitrate in the FeMo-co of nitrogenases. In the structures of K4(NH4)2[Mo2O2S2(C6H4O7)2].

Ammonium 4-nitrophenylarsonate.

In the crystal structure of the title compound, (NH(4))[AsO(2)(OH)(C(6)H(4)NO(2))], the 4-nitrophenylarsonate anions and ammonium cations are linked through hydrogen bonds to form infinite chains along the b axis. The hydroxyl O atom of the 4-nitrophenylarsonate anion acts as both an acceptor and a donor of hydrogen bonds. All atoms are located in general positions.