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By introducing three pyridyl-1H-tetrazole derivatives to Keggin–Ag-(1,10-phenanthroline) system, five new polyoxometalate-based inorganic–organic hybrid compounds with different dimensionalities and structures, [Ag3(4-ptz)2Na(phen)(HPMo12O40)]·2H2O (1), [Ag4(3-ptz)2(phen)2(HPMo12O40)] (2), [Ag4(3-ptz)2(phen)2(HVW12O40)] (3), [Ag3(3-bptzb)(phen)2(PMo12O40)] (4) and [Ag3(3-bptzb)(phen)2(VW12O40)] (5) (phen = 1,10-phenanthroline, x-ptzH = 5-(x-pyridyl)-1H-tetrazole (x = 3, 4), 3-bptzb = 1,4-bis(5-(3-pyridyl)-tetrazolyl)butane), have been synthesized under hydrothermal conditions. Compound1is a 1-D belt architecture constructed from an Ag-4-ptz metal–organic chain and two Ag–PMo12O40–Na–phen inorganic–organic chains. When 3-ptzH was introduced as secondary ligand in2and3instead of 4-ptzH, two isostructural architectures were obtained, which contain a 1-D zigzag Ag-3-ptz chain with phen ligands hanging on both sides of the chain. The Keggin anions connect adjacent Ag-3-ptz chains to construct 2-D networks. When the flexible 3-bptzb was selected, isostructural4and5with 2-D networks were obtained, which were constructed from binuclear subunits and Keggin–Ag inorganic chains. The influence of three pyridyl-1H-tetrazole derivatives as secondary ligands on the dimensionalities and architectures of1–5was discussed. The electrochemical and photocatalytic properties of the compounds were investigated. [ABSTRACT FROM PUBLISHER]

A Keggin-type polyoxometalate (POM)-based complex, [Ag5(L)3(H2O)2]·6H2O (1) (L = N,N′-bis(3-pyridinecarboxamide)-1,2-ethane), has been hydrothermally synthesized. Compound1shows a 3D + 3D interpenetrating network with a (3,4,4,4)-connected (4 × 62)2(42 × 62 × 82)(65 × 8)2topology, and it represents the first example of interpenetrating POM-based complex based on flexible bis-pyridyl-bis-amide ligands. Moreover, the electrochemical behavior and luminescence of1have been investigated. [ABSTRACT FROM AUTHOR]

Four coordination polymers, [Cu(4-dpyh)0.5(1,2-BDC)(H2O)3]·H2O (1), [Cu(4-dpyh)(1,3-BDC)(H2O)] (2), [Cd(3-dpyh)0.5(1,3-BDC)(H2O)2]·H2O (3), and [Zn(3-dpyh)(1,3-BDC)]·3H2O (4) [4-dpyh = N,N′-bis(4-pyridinecarboxamide)-1,6-hexane, 3-dpyh = N,N′-bis(3-pyridinecarboxamide)-1,6-hexane, 1,2-H2BDC = 1,2-benzenedicarboxylic acid and 1,3-H2BDC = 1,3-benzenedicarboxylic acid], have been hydrothermally synthesized. X-ray diffraction analyses reveal that1is a discrete [Cu2(4-dpyh)(1,2-BDC)2] dinuclear structure. Compound2exhibits a 2-D grid layer constructed from 1-D linear [Cu(1,3-BDC)]nchains and [Cu(4-dpyh)]nchains. Compound3features a 1-D ladder-like chain formed by the 1-D linear [Cd(1,3-BDC)]nchains and 3-dpyh bridging ligands. Compound4displays a 2-D undulated layer containing meso-helical [Zn(3-dpyh)]nchains and linear [Zn(1,3-BDC)]nchains. The neighboring dinuclear complexes for1, adjacent chains for3, and adjacent layers for2and4are further linked by hydrogen bonding interactions to form 2-D (for1) or 3-D supramolecular networks (for2–4). The influences of the different dicarboxylates and metal on the structures of1–4have been discussed. The electrochemical behaviors of1and2, the thermal stabilities and fluorescent properties of1–4, and the fluorescent selectivities of3and4have been investigated. Four new metal–organic coordination polymers have been hydrothermally synthesized by the flexible bis-pyridyl-bis-amide ligands and two different aromatic dicarboxylates. The influences of the different dicarboxylates and central metal ions on the structures of1–4have been reported. Moreover, the electrochemical behaviors of1and2, thermal stabilities, and the fluorescent properties of1–4have been investigated. [ABSTRACT FROM AUTHOR]

Two metal–organic coordination polymers, [Cu3(4-bpcb)2(1,2,4-btc)2(H2O)2] (1) and [Cu3(3-bpcb)3(btec)1.5] (2), have been synthesized from hydrothermal reaction of copper chloride with mixed ligands [4-bpcb = N,N′-bis(4-pyridinecarboxamide)-1,4-benzene, 3-bpcb = N,N′-bis(3-pyridinecarboxamide)-1,4-benzene, 1,2,4-H3btc = 1,2,4-benzenetricarboxylic acid, and H4btec = 1,2,4,5-benzenetetracarboxylic acid]. X-ray diffraction analysis reveals that1exhibits a 2-D layer structure and2possesses a three-dimensional (3-D) network. In1and2, CuIIions are connected by bridging 1,2,4-btc or btec to form 2-D polymeric layers. Cu-1,2,4-btc layer does not propagate into a 3-D coordination framework in1due to 4-bpcb showing monodentate coordination (via ligation of only one pyridyl nitrogen). In2, Cu-btec 2-D layers are further extended into a 3-D network with (64.82)3topology by 3-bpcb ligand inμ2-bridging coordination (via ligation of two pyridyl nitrogens). The different structures of the two complexes illustrate the influence of different polycarboxylates and N-donor positions of organic ligands on the formation of such coordination architectures. Moreover, the thermal properties and electrochemical properties of the copper complexes bulk-modified carbon paste electrodes have been studied. [ABSTRACT FROM AUTHOR]