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Through adjustment of the pH value of the reaction system, two series of 3 D lanthanide(III)-copper(I) coordination polymers, namely [Ln2(na)7Cu6Br5(H2O)2] [Ln=La ( 1), Ce ( 2), Pr ( 3), Nd ( 4), Sm ( 5), Eu ( 6), Gd ( 7), Tb ( 8)] and [La2(na)7Cu3Br2(H2O)2]⋅H2O ( 9) (na−=nicotinate), are synthesized hydrothermally and characterized fully. It is worth nothing that these two series of heterometallic compounds are constructed from similar ladder-like Ln-organic chains, but different copper(I) halide clusters. The luminescence properties of the compounds with Nd ( 4), Eu ( 6), and Tb ( 8) are also investigated. [ABSTRACT FROM AUTHOR]

The hydrothermal reaction of rare earth nitrates, CuCN, 2,7-naphthalenedisulfonate (2,7-nds), and isonicotinic acid (Hina) affords a new family of 3-D heterometallic 3d–4f coordination polymers, [Ln2Cu(2,7-nds)2(ina)4(H2O)4]·4H2O (Ln = Nd (1), Sm (2), Eu (3), Gd (4); 2,7-nds = 2,7-naphthalenedisulfonate, Hina = isonicotinic acid). Complexes1–4are structurally characterized by single crystal X-ray diffraction, elemental analysis, FT-IR spectroscopy (IR), powder X-ray diffraction, and thermogravimetric analyses. X-ray crystal structure analyses reveal that1–4are isomorphous with dinuclear subunit [Sm2(ina)4] binding Cu ions to generate 2-D networks. Such 2-D networks are pillared by linking 2,7-nds ligands to result in the 3-D layer-pillared Ln(III)–Cu(II) coordination architectures. The valence of Cu salts changed in the reaction. In addition, the luminescence properties of1–3and the magnetic properties of3and4have also been investigated. [ABSTRACT FROM PUBLISHER]

Two 2D zinc(II) layered coordination polymer compounds [Zn2(atz)2(na)2] n ( 1), and [Zn(atz)(ina)] n ( 2) (Hatz = 3-amino-1H-1, 2, 4-triazole, na = nicotinic acid, ina = isonicotinic acid) were synthesized and structurally characterized by elemental analysis, FT-IR, thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction. The interconnection of a coplanar six-membered hexagonal ring and a 16-membered non-planar chair-like ring results in a 2D sheet with (4, 82) topological network. Hydrogen bonds connect the neighboring planes into 3D supramolecular architectures. Furthermore, both complexes exhibit strong luminescent properties in the solid state at room temperature. [ABSTRACT FROM AUTHOR]

Reactions of H3tda (H3tda = 1H-1, 2, 3-triazole-4, 5-dicarboxylic acid) with Sm(NO3)3 ·6H2O, Eu(NO3)3 ·6H2O, and Tb(NO3)3 ·6H2O, in the presence of NaOH under hydrothermal conditions, produced three new coordination polymers, [ Ln2(tda)2(H2O)3] ·5H2O [ Ln = Sm ( 1), Eu ( 2), Tb ( 3)]. These compounds were structurally characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), PXRD and single-crystal X-ray diffraction. The single-crystal X-ray diffraction studies of compounds 1- 3 reveal that all compounds are three-dimensional porous structures with chiral frameworks. Furthermore, the luminescence studies of compound 2 and 3 in the solid state reveal that they are potential luminescent materials at room temperature. [ABSTRACT FROM AUTHOR]

Abstract: Four novel functional supramolecular metal–organic coordination polymers, [Cd2Cl3(IP)2(NIPH)2](1), [Zn2(IP)2(μ2-SO4)2(NIPH)2]·2H2O(2), [Cd(IP)2(BPDC)](3), [Zn2(IP)2(NDC)2](4) (IP=1-H-imidazo[4,5-f][1,10]-phenanthroline, H2NIPH=5-nitro-isophthalic acid, H2BPDC=4,4′-biphenyldicarboxylic acid, H2NDC=2,6-naphthalenedicarboxylic acid), have been obtained through three types of dicarboxylate linkers. All the four compounds are extended into a 3-D supramolecular framework by hydrogen bonds or weak aromatic interactions. The different structures demonstrate the effect of the dicarboxylate ligands on the formation of such coordination architectures. Compound 1 is a 1-D double-stranded loop-like chain with repeated [Cd4(Cl)4]4+ units connected by H2NIPH ligands. In compound 2, there are two indie 1D zigzag chains jointed by sulfate anions with μ2-bridging mode. With different metal centers, compounds 1 and 2 hold different crystal structures. With different auxiliary dicarboxylate ligands, compounds 3 and 4 exhibit disparate 1D chains. The fluorescence property and thermal stability of all complexes are also investigated. [Copyright &y& Elsevier]

Two kinds of three-dimensional (3D) coordination frameworks from monometallic to heterometallic, including a charming 3D monometallic complex, namely, [Eu2(mpda)3(H2O)4]n (1) and the first series of novel 3D heterometallic 4d-4f coordination frameworks based on 2,6-dimethylpyridine-3,5-dicarboxylic acid, namely, [Ln2Cd2(mpda)2(bdc)2(SO4)2(H2O)6]n [Ln=Sm(2), Eu(3), Gd(4), Tb(5), Dy(6); mpda=2,6-dimethylpyridine-3,5-dicarboxylic acid; bdc=1,4-benzenedicarboxylic acid] have been successfully synthesized under hydrothermal conditions and structurally characterized. Crystal 1 is featured by its interesting 3D chain-layer construction which is formed by the alternative arrangement of chains and layers and exhibits 2-nodal 5, 6-connected 3D network with the Schlafli symbol of {33.43.55.64}{36.46.53}. Complexes 2-6 are isostructural and it reveals that these 3D heterometallic compounds are firstly built by H2mpda ligand. What is worth mentioning is that anionic ligand SO42− plays a crucial function in the construction building. The two-dimensional (2D) lanthanide-transition heterometallic bilayers [Ln2Cd2(mpda)2(bdc)2]n are pillared by SO42− subunits forming mixed-ligand complexes with a pillared-layer 3D structure. Complexes 2-6 feature 4-nodal 3, 4, 5, 6-connected 3D frameworks with {4.82}{4.84.10}{42.810.102.12}{42.88} topology. All the complexes are characterized by elemental analyses, FT-IR spectroscopy, Powder X-ray diffraction (PXRD) and thermogravimetric analyses (TGA). Furthermore, the luminescence properties of compounds 1, 3, and 5 and the magnetic properties of complexes 4 and 6 were also investigated in detail. [ABSTRACT FROM AUTHOR]

Abstract: The first example of 3D heterometallic 4d–4f 2,7-naphthanlenedisulfonate compounds [LnAg2(2,7-NDS)(IN)3] (Ln=Sm (1), Eu (2), Gd (3), Tb (4), Dy(5); 2,7-NDS=2,7-naphthanlenedisulfonate; IN=isonicotinic acid) has been synthesized via hydrothermal reaction and characterized by single crystal X-ray diffraction, elemental analyses, FT-IR spectroscopy, powder X-ray diffraction(PXRD) and thermogravimetric analyses (TGA). X-Ray structural analysis reveals that compounds 1–5 exhibit same well-organized 3D coordination frameworks that are built up by 2D elliptical cylinder shaped [LnAg2(2,7-NDS)(IN)3] layers which are constructed by 1D anionic chains [Ln(2,7-NDS)(IN)3]2− linking the adjacent Ag(I) ions, and [LnAg(μ2-O)2] units, possessing a 7-connected topology with the Schläfli symbol of {33;411;56;6}. Furthermore, the luminescence properties of compounds 2 and 4 and the magnetic properties of compounds 3 and 5 were investigated. [Copyright &y& Elsevier]