A helical zinc(II) coordination polymer assembled from 1,3-bis[(pyridin-3-yl)methoxy]benzene and benzene-1,4-dicarboxylic acid.

In catena-poly[[aqua[1,3-bis(pyridine-3-ylmethoxy)benzene-κN]zinc(II)]-μ2-benzene-1,4-dicarboxylato-κ(2)O(1):O(4)], [Zn(C8H4O4)(C18H16N2O2)(H2O)]n, each Zn(II) centre is tetrahedrally coordinated by two O atoms of bridging carboxylate groups from two benzene-1,4-dicarboxylate anions (denoted L(2-)), one O atom from a water molecule and one N atom from a 1,3-bis[(pyridin-3-yl)methoxy]benzene ligand (denoted bpmb). (Aqua)O-H···N hydrogen-bonding interactions induce the formation of one-dimensional helical [Zn(L)(bpmb)(H2O)]n chains which are interlinked through (aqua)O-H···O hydrogen-bonding interactions, producing two-dimensional corrugated sheets.

Regioselective C-H imidation of five-membered heterocyclic compounds through a metal catalytic or organocatalytic approach.

An efficient method for the synthesis of 2-amino and β-amino five-membered heterocyclic derivatives that are closely related to a variety of biologically active natural products is described. Regioselectivity was achieved through a metal catalytic or organocatalytic approach. Preliminary studies on the reaction mechanism suggest a radical imidation pathway; however, further studies are needed to verify the mechanism.

The three-dimensional coordination polymer poly[[aqua[μ4-2,2'-(diazene-1,2-diyl)dibenzoato]lead(II)] 1,2-bis(pyridin-4-yl)ethylene hemisolvate].

A novel three-dimensional coordination polymer, {[Pb(C14H8N2O4)(H2O)]·0.5C12H10N2}n, has been synthesized by hydrothermal reaction of Pb(OAc)2·3H2O (OAc is acetate), 2,2'-(diazene-1,2-diyl)dibenzoic acid (H2L) and 1,2-bis(pyridin-4-yl)ethylene (bpe). The asymmetric unit contains a crystallographically independent Pb(II) cation, one L(2-) ligand, an aqua ligand and half a bpe molecule.

Three coordination polymers constructed from various polynuclear clusters spaced by 2,2'-azodibenzoic acid: syntheses and fluorescent properties.

Solvothermal reactions of M(OAc)2·2H2O (M = Zn, Cd, Pb) with 2,2'-azodibenzoic acid (H2L) in MeOH-H2O (MeOH = methanol) at 120 °C gave rise to three coordination polymers, [Zn12(μ4-O)3L9]n (1), [CdL(H2O)]n (2) and [Pb3(μ4-O)L2]n (3). Compounds 1-3 are characterized by elemental analysis, IR, powder X-ray diffraction and single-crystal X-ray diffraction. Compound 1 has two similar tetranuclear [Zn4(μ4-O)(μ2-CO2)6] units as nodes and displays an intriguing three-dimensional (3D) 6-connected network with a 4(12)6(3) topology.

Electrochemical detection of β-amyloid peptides on electrode covered with N-terminus-specific antibody based on electrocatalytic O2 reduction by Aβ(1-16)-heme-modified gold nanoparticles.

β-Amyloid (Aβ) peptides are believed to be important for the diagnosis and prognosis of Alzheimer's disease (AD) serving as reliable molecular biomarkers. In this work, we reported a simple and sensitive electrochemical strategy for the detection of total Aβ peptides using gold nanoparticles modified with Aβ(1-16)-heme (denoted as Aβ(1-16)-heme-AuNPs). Monoclonal antibody (mAb) specific to the common N-terminus of Aβ was immobilized onto gold electrode for the capture of Aβ(1-16)-heme-AuNPs.

Assembly and spontaneous resolution of the chiral inorganic polyoxometalates-based frameworks via helical chains association.

Two pairs of enantiomerically pure three-dimensional (3D) chiral polyoxometalate (POM) framework materials l,d-[K(H2O)]6·[H2GeW12O40]3·35H2O (1a and 1b) and l,d-[K(H2O)]6·[H2SiW12O40]3·29H2O (2a and 2b) based on inorganic achiral building blocks, have been synthesized and characterized by X-ray crystallography, elemental analysis, powder X-ray diffraction (PXRD), UV-Vis spectroscopy, circular dichroism (CD) spectra. Single-crystal X-ray diffraction analyses revealed that 1a and 1b, 2a and 2b are enantiomers, respectively. In 1a and 1b, 2a and 2b, {K(H2O)}n link terminal oxygen and μ2-bridging oxygen of Keggin-type polyanion moieties to generate 1D 31 helical infinite chiral chains, which are further connected by the achiral Keggin-type polyoxoanions to form 3D 4,8-connected chiral self-assembly frameworks with {4(12)·6(10)·8(6)}{4(6)}2 topology.

A polyhedron-based metal-organic framework with a reo-e net.

A polyhedron-based metal-organic framework has been designed and constructed with a reo-e net, which is constructed from trinuclear nickel clusters and mixed ligands (copolymerization pattern). It comprises three kinds of polyhedra, which are the hexahedron, cuboctahedron and rhombicuboctahedron.

A sodalite-type porous metal-organic framework with polyoxometalate templates: adsorption and decomposition of dimethyl methylphosphonate.

A sodalite-type porous metal-organic framework with polyoxometalate templates, H(3)[(Cu(4)Cl)(3)(BTC)(8)](2)[PW(12)O(40)]·(C(4)H(12)N)(6)·3H(2)O (NENU-11; BTC = 1,3,5-benzenetricarboxylate), was obtained by a hydrothermal reaction. As a reasonable candidate for eliminating nerve gas, NENU-11 displays good adsorption behavior for dimethyl methylphosphonate (15.5 molecules per formula unit).

Reactivity of polyoxoniobates in acidic solution: controllable assembly and disassembly based on niobium-substituted germanotungstates.

The reactivity of polyoxoniobates has been studied in acidic solution by grafting niobium onto trivacant Keggin-type germanotungstates. Four niobium-containing compounds were obtained in the course of this study. Cs(6.

Coordination between [H2P2W12O48]12- and antimony(III): synthesis and characterization of sandwich complex derived from the new {P2W13O51} fragment.

A sandwich-type anionic cluster of a new lacunary building block [P(2)W(13)O(51)](14-) has been prepared: [H(6){P(2)W(13)O(51)}(2)Sb(4)](10-) (1) was synthesized in a one-pot self-assembly reaction of [H(2)P(2)W(12)O(48)](12-) with C(4)H(4)KO(7)Sb.0.5H(2)O and characterized by single-crystal X-ray analysis, IR, thermogravimetric analysis, elemental analysis, UV, NMR and electrochemistry.