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The polymeric title complex, [Co(C8H8O5)(H2O)2]n was synthesized by reaction of cobalt acetate with 7-oxabicyclo­[2,2,1]heptane-2,3-dicarb­oxy­lic anhydride. The CoII ion is six-coordinated in a distorted octa­hedral environment, binding to two water O atoms, to the ether O atom of the bicyclo­heptane unit, to two carboxyl­ate O atoms from two different carboxyl­ate groups of the same anion and to one carboxyl­ate O atom from a symmetry-related anion. The bridging character of the dianion leads to the formation of ribbons along [001]. The ribbons are linked into a layered network parallel to (010) by several O—H...O hydrogen-bonding inter­actions involving the coordinating water mol­ecules as donors and the carboxyl­ate O atoms of neighbouring ribbons as acceptors. The crystal under investigation was an inversion twin.

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In the title hydrated mol­ecular salt, (C7H7N2S)2[Zn(C8H8O5)2]·6H2O, which is isotypic with its MnII, CoII and NiII analogues, the Zn2+ ion lies on a crystallographic inversion centre and a distorted ZnO6 octa­hedral coordination geometry arises from the two doubly deprotonated O,O′,O′′-tridentate ligands. In the crystal, the components are linked by N—H...Oa, N—H...Ow, Ow—H...Oa and Ow—H...Ow hydrogen bonds (w = water and a = anion).

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In the structure of the title complex, (C7H7N2S)2[Cd(C8H8O5)2]·6H2O, the CdII atom is located on an inversion center and is O,O′,O′′-chelated by two symmetry-related 7-oxabicyclo­[2.2.1]heptane-2,3-dicarboxyl­ate ligands in a distorted octa­hedral geometry. The 2-amino­benzothia­zolium cation links with the Cd complex anion via N—H...O hydrogen bonding. Extensive O—H...O and N—H...O hydrogen bonds involving lattice water mol­ecules occur in the crystal structure.
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