Gd(1)-O(12) 2.373(2) Gd(2)-O(5) 2.372(2) Gd(1)-O(2) 2.407(2) Gd(2)-O(9) 2.385(3) Gd(1)-O(16) i 2.411(2) Gd(2)-O(18) 2.416(2) Gd(1)-O(15) i 2.435(2) Gd(2)-O(14) 2.440(2) Gd(1)-O(7) ii 2.482(2) Gd(2)-O(13) 2.442(3) Gd(1)-O(17) 2.489(2) Gd(2)-O(3) iii 2.454(3) Gd(1)-O(8) 2.562(3) Gd(2)-O(4) 2.540(3) Gd(1)-O(7) 2.568(2) Gd(2)-O(3) 2.744(3) Gd(2)-O(10) 2.364(2) i x-1,y,z ii -x+1,-y+1,-z+1 iii -x+2,-y+2,-z

No abstract

In the title compound, poly[hexaaquabis[mu(4)-3,5-bis(carboxylatomethoxy)benzoato]trizinc(II)], [Zn(3)(C(11)H(7)O(8))(2)(H(2)O)(6)](n), there are two crystallographically distinct Zn(II) cations which are bridged by polycarboxylate ligands in a mu(4)-bridging mode. A pair of ligands bridges adjacent Zn atoms to give centrosymmetric dimetal building blocks which act as four-connected nodes to be further interlinked into a two-dimensional double-layered framework with (4,4) topology. Other Zn atoms, lying on inversion centres, occupy the cavities of this topological structure. This submission shows a versatile polycarboxylate ligand with rigid and flexible functional groups, the co-operation and complementarity of which would meet the coordination requirements of a variety of topological structures.

In the centrosymmetric dinuclear title compound, [Cu2(C2H3N)2(C18H10N4)2(C32H30N2P2)](BF4)2, the CuI centre is coordinated by two N atoms from a dipyridophenazine ligand, one P atom from an N,N′-bis­[(diphenyl­phosphan­yl)meth­yl]benzene-1,4-diamine (bpbda) ligand, and one N atom from an acetonitrile mol­ecule in a distorted tetra­hedral geometry. The bpbda ligand, lying on an inversion center, bridges two CuI centres into a Z-shaped complex. Intra­molecular π–π inter­actions between the dipyridophenazine ligand and the benzene ring of the bpbda ligand are observed [centroid–centroid distance = 3.459 (3) Å]. The crystal structure also involves inter­molecular π–π inter­actions between the dipyridophenazine ligands [centroid–centroid distance = 3.506 (3) Å], which lead to a one-dimensional supra­molecular structure.

The asymmetric unit of the title compound, [Zn(C12H11N2O4)2(H2O)4]·4H2O, contains one-half of the complex mol­ecule and two uncoordin­ated water mol­ecules. The four water O atoms in the equatorial plane around the ZnII centre ( symmetry) form a distorted square-planar arrangement, while the distorted octa­hedral coordination geometry is completed by the O atoms of the zwitterionic 2-methyl­benzimidazolium-1,3-diacetate ligands in the axial positions. The benzimidazole ring system is planar, with a maximum deviation of 0.041 (3) Å. Intra­molecular O—H⋯O hydrogen bonding results in the formation of a non-planar six-membered ring. In the crystal structure, strong intra- and inter­molecular O—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional network. π–π contacts between benzimidazole rings [centroid–centroid distance = 3.899 (1) Å] may further stabilize the structure.