A new family of polyoxometalate compounds built up of Preyssler anions and trivalent lanthanide cations

Four new polyoxometalate compounds built on Preyssler anions and trivalent lanthanide cations, Na₂[{Ce(H₂O)₈}₄{Na(H₂O)P₅W₃₀O₁₁₀}] · 12H₂O (1), H₄Na₄[Nd₂(H₂O)₁₄{Na(H₂O)P₅W₃₀O₁₁₀}] · 22H₂O (2), K₂Na[Eu₃(H₂O)₁₄(HNA)₃{Eu(H₂O)P₅W₃₀O₁₁₀}] · 3H₂O (3 NA = nicotinic acid) and H₂[Ce₄(H₂O)₁₆(HNA)₆{Na(H₂O)P₅W₃₀O₁₁₀}] · 12H₂O (4) have been synthesized and characterized by elemental analysis, IR, TG and single crystal X-ray diffraction. Compound 1 exhibits a tetrasupporting polyoxometalate cluster structure where four {Ce(H₂O)₈}³⁺ fragments are supported on the [Na(H₂O)P₅W₃₀O₁₁₀]¹⁴⁻ cluster. Compound 2 shows a one-dimensional chain structure built from [Na(H₂O)P₅W₃₀O₁₁₀]¹⁴⁻ clusters linked by Nd³⁺ cations. Compound 3 displays a one-dimensional chain structure constructed of [Eu(H₂O)P₅W₃₀O₁₁₀]¹²⁻ clusters bridged by Eu³⁺ cations. Compound 4 has a 2D network formed by 1D chains and {Ce₂(H₂O)₆(HNA)₆}⁶⁺ linkers. Compounds 2-4 represent the first extended structures based on Preyssler anions. In addition, the fluorescent activity of compound 3 is reported.     

Two new extended frameworks constructed from the sandwiching polytungstoarsenate clusters

Two new extended frameworks based on two different sandwich-type polytungstoarsenates have been synthesized under routine conditions. The reaction of Na₉[As^IIIW₉O₃₃]·19.5H₂O, MnSO₄·H₂O and citric acid in a weak acidic aqueous solution at pH = 4.23 led to the isolation of a new extended sandwich-type compound {K₃Na₈[{Mn^II(H₂O)}_2.5{(WO)(H₂O)}_0.5(AsW₉O₃₃)₂]·12.5H₂O}_n (1). In compound 1, each sandwiching polyoxoanion [{Mn^II(H₂O)}_2.5{(WO)(H₂O)}_0.5(AsW₉O₃₃)₂]¹¹⁻ acts as a quadridentate ligand to connect with four neighbors via the mode of {W-O-Mn}, finally leading to an interesting 2D network. The reaction of Na₈[HAsW₉O₃₄]·11H₂O, CeCl₃·7H₂O and hexamethylenetetramine in an aqueous solution with pH = 5.07 resulted in the obtainment of a polytungstoarsenate-based extended compound [HMTA-CH₃]₂[HMTA]K₂Na₇[Ce(AsW₁₁O₃₉)₂]·19H₂O(2) (HMTA-CH₃ = methyl-hexamethylenetetraamine; HMTA = hexamethylenetetraamine). In 2, the polyoxoanions [Ce(AsW₁₁O₃₉)₂]¹¹⁻ construct a new extended structure through coordinating to the {KO₅(H₂O)[HMTA-CH₃]} and {KO₄(H₂O)₂[HMTA]} units. The two compounds are characterized by elemental analyses, IR, the diffuse reflectance UV-Vis spectra, PXRD and TG analyses. The electrochemical and electrocatalytical properties of 1 and 2, as well as the fluorescent property of 2 were also investigated.     

Niobium-substituted arsenotungstates: Controllable transformation between monomers and tetramer

Three niobium-containing arsenotungstates have been synthesized for the first time: peroxoniobium-containing Cs₅K[AsW₉(NbO₂)₃O₃₇]·7H₂O (1), peroxo-free Cs_5.5Na_0.5[AsW₉Nb₃O₄₀]·17H₂O (2), and tetramer Cs₁₀K₃H₃[As₄W₃₆Nb₁₆O₁₆₆]·28H₂O (3). Both monomers 1 and 2 can assemble into tetramer 3 in acidic conditions, and 3 can transform to 1 or 2 by adding H₂O₂ or adjusting the pH value. Comparing the Nb-containing POM systems of A-α-XW₉ (X = Si, Ge, As), although they are different only in heteroatoms, there are remarkable differences in reaction conditions and reactivity. The ¹⁸³W NMR spectra of 1, the UV-Vis spectra of 1-2 along with the IR spectra and thermal stability of 1-3 have been studied and compared with their Ge or Si analogs. The electrochemical properties of 1-3 have also been investigated and the cyclic voltammograms of 3 indicate good electrocatalytic activity towards the reduction of nitrite.     

A novel one-dimensional chain-like structure based on sandwich-type tungstoantimonate and cadmium(II)

A novel cadmium-substituted tungstoantimonate [Sb₂W₂₁Cd(OH)₂O₇₃]¹⁴⁻ (1), has been synthesized in aqueous solution and characterized by IR, elemental analysis, TGA and cyclic voltammetry (CV). Single-crystal X-ray analysis was carried out on K_4.5Na_9.5[Sb₂W₂₁Cd(OH)₂O₇₃] · 31H₂O (1a). Polyanion 1 consists of two Cd(W) ions linked to a [Sb₂W₂₀O₇₀]¹⁴⁻ fragment via Cd-O(W) bonds leading to a sandwich-type structure. Interestingly, the polyanion [Sb₂W₂₁Cd(OH)₂O₇₃]¹⁴⁻ (1) as basic building unit is assembled into a one-dimensional (1D) chain-like structure by Cd and W atoms sharing the same site with the 50% occupations, respectively. The electrochemical behavior of 1 was investigated in buffer solution (pH 3.0) by CV. In the potential range between −0.75 and 0.2 V, the compound 1 exhibits the successive redox processes of the addenda atoms (W). The electrocatalytic experiments of the compound show that this compound has good electrocatalytic activity towards the reduction of H₂O₂.     

An equatorial tri-iron substituted Wells-Dawson type tungstophosphate with magnetic and bifunctional electrocatalytic properties

Interaction of the hexa-lacunary polyanion precursor [α-H₂P₂W₁₂O₄₈]¹²⁻ and the Fe^III in aqueous solution results in the formation of an equatorial tri-iron substituted Wells-Dawson type compound, K₄Cs₂Fe₂[P₂W₁₅(FeOH)₃O₅₉]·22H₂O (1). Compound 1 was characterized by IR, elemental, single-crystal X-ray diffraction, thermogravimetric, magnetic, as well as electrochemical analysis. The polyoxoanion [P₂W₁₅(FeOH)₃O₅₉]¹²⁻ can be viewed as a derivative of the parent polyoxoanion [α-P₂W₁₈O₆₂]⁶⁻ by removal of three belt WO groups and then inhabited by three FeOH groups. The compound 1-modified carbon paste electrode (1-CPE) presents good electrocatalytic activity not only toward the reduction of nitrite which is attributed to the function of tungstophosphate, but also toward the oxidation of ascorbic acid which is primarily attributed to the function of Fe^III. The magnetic properties of 1 have been studied by magnetic susceptibility and fitted according to an isotropic exchange model. Compound 1 exhibits strong antiferromagnetic spin exchange interactions between the Fe^III centers.     

Assembly of three novel 2D frameworks with helical chains based on [H2W12O40] clusters and lanthanide - Organic complexes

Three novel polyoxotungstate-based rare earth compounds, [(C₆H₅NO₂)Ln(H₂O)₅]₂[H₂W₁₂O₄₀] · nH₂O (Ln = Ce³⁺ (1), Pr³⁺(2), n = 7; Nd³⁺ (3), n = 6), have been synthesized in aqueous solution and characterized by single-crystal X-ray diffraction, elemental analysis, IR spectra and TG analysis. The structural feature of compounds 1-3 is that the α-metatungstate cluster [H₂W₁₂O₄₀]⁶⁻ anions are linked by the lanthanide (Ln) cation-organic coordination complexes, resulting in a two-dimensional (2D) structure with helical chains. The magnetic properties of compounds 1 and 2 have been studied by measuring their magnetic susceptibility in the temperature range 2-300 K, indicating the existence of spin-orbital coupling interactions and antiferromagnetic response. Furthermore, the electrochemical properties of 1-3 were studied.     

Hybrid organic-inorganic assemblies built up from saturated heteropolyoxoanions and copper coordination polymers with mixed 4,4′-bipyridine and 2,2′-bipyridine ligands

Three new organic-inorganic hybrid compounds [Cu^I(2,2′-bipy)(4,4′-bipy)_0.5]₂[Cu^I(2,2′-bipy)(4,4′-Hbipy)][Cu^I(4,4′-bipy)]₂[P₂W₁₈O₆₂] · 3H₂O (1), [Cu^I(2,2′-bipy)(4,4′-bipy)_0.5]₂[Cu^I(4,4′-bipy)]₂[PW₁₂O₄₀] · 0.25H₂O (2), and[Cu^I(4,4′-bipy)]₃[PMo₁₂O₄₀] · en · 3H₂O (3) (2,2′- bipy = 2,2′-bipyridine, 4,4′-bipy = 4,4′-bipyridine), have been hydrothermally synthesized. Compound 1 represents the first 1D ladderlike structure formed by Dawson-type polyoxoanion [P₂W₁₈O₆₂]⁶⁻ and coordination polymer with mixed 4,4′-bipy and 2,2′-bipy ligands. The novel structure of 2 is composed of 1D hybrid zigzag chains linked by chains into a 3D framework. In compound 3, the [PMo₁₂O₄₀]³⁻ clusters are hung on chains to form a new 1D chain.     

Zirconium and hafnium aqua complexes [(H2O)3M(P2W17O61)]: Synthesis, characterization and substitution of water by chiral ligand

The hydroxocomplexes [{(H₂O)M(μ₂-OH)(P₂W₁₇O₆₁)}₂]¹⁴⁻ (M = Zr, Hf) in HCl undergo cleavage of the hydroxo bridges with the formation of monomeric species [(H₂O)₃M(P₂W₁₇O₆₁)]⁶⁻. In the case of Hf single crystals of the composition (Me₂NH₂)_5.5(H)_1.5[(Hf(H₂O)₃)_0.9(WO)_0.1{P₂W₁₇O₆₁}]Cl·9.5H₂O (1), as the result of co-crystallization of [(H₂O)₃Hf(P₂W₁₇O₆₁)]⁶⁻ and [P₂W₁₈O₆₂]⁶⁻ salts, were isolated from these solutions and structurally characterized. Zr gives (Me₂NH₂)₂(H)₄[{(H₂O)₂ZrP₂W₁₇O₆₁}]·8.67H₂O (2), in whose structure chiral polymeric chains {[(H₂O)₂M(P₂W₁₇O₆₁)]}_n⁶ⁿ⁻ are present. Under hydrothermal conditions the water molecules in [(H₂O)₃M(P₂W₁₇O₆₁)]⁶⁻ are replaced by l-malic acid with the formation of stable chiral polyoxoanions, isolated as (NH₂Me₂)₈[M(L-ООССН(ОН)СН₂СОО)P₂W₁₇O₆₁]·7·9H₂O (M = Zr, 3; M = Hf, 4). The structures of 1, 2 and 3 were determined; 3 and 4 were found to be isostructural. The products were also characterized by elemental analysis, thermogravimetry and IR-spectroscopy.     

A new (8,3)-connected anionic 3-D open-framework based on paradodecatungstate and Cu linkers

The hydrothermal reaction of [H₂W₁₂O₄₂]¹⁰⁻ precursors and CuCl₂ in a CH₃COOK/CH₃COOH solution (pH 3.5) led to the isolation of a new compound, KNa₃[Cu(H₂O)₂{Cu(H₂O)₃}₂(H₂W₁₂O₄₂)] · 16H₂O (1). Compound 1 possesses a new anionic three-dimensional (3-D) open-framework based on the [H₂W₁₂O₄₂]¹⁰⁻ building blocks and Cu^II linkers. This anionic 3-D framework represents the first example of a (8,3)-connected structural topology in POM-based solid materials. The magnetic behavior of 1 exhibits weak antiferromagnetic interaction.     

Studies on Zn(II) and Cd(II) heteroligand complexes with RC(S)NHP(O)(OiPr)2 (R = Ph, NH2, PhNH) and α-diimine (bpy and phen) ligands. C-Cl bond cleavage of CH2Cl2 by [Zn(phen){PhC(S)NP(O)(OiPr)2}2]

The reaction of [ZnL^I,II₂] (L^I = [NH₂C(S)NP(O)(OiPr)₂]⁻; L^II = [PhNHC(S)NP(O)(OiPr)₂]⁻) or [Cd₂L^IV₄] (L^IV = [PhC(S)NP(O)(OiPr)₂]⁻) with 2,2′-bipyridine (bpy) or 1,10-phenanthroline (phen) leads to the heteroligand complexes [Zn(bpy)L^I,II₂], [Zn(phen)L^I,II₂], [Cd(bpy)L^IV₂] or [Cd(phen)L^IV₂], respectively. The introduction of the diimine ligands into the coordination sphere of the metal cation provokes a change from 1,5-O,S- to 1,3-N,S-coordination of the anionic ligands for Zn but not for the Cd species. The reaction of [Zn(phen)L^IV₂] (L^IV = PhC(S)NP(O)(OiPr)₂⁻) with CH₂Cl₂ cleaves the chlorine atoms from CH₂Cl₂ and leads to the formation of [Zn(phen)L^IVCl] and S,S′-bis(benzimidothio-N-diisopropoxyphosphoryl)methane (L^IV-CH₂-L^IV) in high yields. Using CHCl₃ or CCl₄ instead of CH₂Cl₂ does not lead to the formation of chlorine substituted products even under reflux conditions. The new compounds were investigated by ¹H and ³¹P{¹H} NMR, IR spectroscopy and microanalysis. Crystal structures of [ZnL^II₂], [Cd(phen)L^IV₂]·CH₂Cl₂, [Zn(bpy)L^I₂] and [Zn(phen)L^IVCl] were elucidated by X-ray diffraction.     

Stereospecific interactions between dinuclear complex cations involving square-planar [Pt(II)(μ-S)2(bpy)] (bpy = 2,2′-bipyridine) frameworks derived from optically active octahedral Co(III) units with d- or l-penicillaminates

The reaction of the octahedral mononuclear complex, trans(N)-[Co(l-pen-N,O,S)₂]⁻ (pen = penicillaminate), with [PtCl₂(bpy)] (bpy = 2,2′-bipyridine) stereoselectively gave an optically active S-bridged dinuclear complex, [Pt(bpy){Co(l-pen)₂}]Cl · 3H₂O (2Cl · 3H₂O), whose structure is enantiomeric to the previously reported [Pt(bpy){Co(d-pen)₂}]Cl · 3H₂O (1Cl · 3H₂O). The mixture of equimolar amounts of 1Cl · 3H₂O and 2Cl · 3H₂O in H₂O crystallizes as [Pt(bpy){Co(d-pen)₂}]_0.5[Pt(bpy){Co(l-pen)₂}]_0.5Cl · 7H₂O (3Cl · 7H₂O), in which the enantiomeric complex cations 1 and 2 are included in the ratio of 1:1. The crystal structures of 2Cl · 3H₂O and 3Cl · 7H₂O were determined by X-ray crystallography, and compared with that of 1Cl · 3H₂O. The structural feature for 2 is essentially consistent with that for 1, except for the absolute configurations around the octahedral Co(III) center. The optically active complex cation 2 exists as a monomer, accompanied by no intermolecular interactions in the π-electronic systems of bpy moieties. In the crystals of 3Cl · 7H₂O, on the other hand, the enantiomeric complex cations, [Pt(bpy){Co(d-pen)₂}]⁺ and [Pt(bpy){Co(l-pen)₂}]⁺, are arranged alternately while overlapping the bpy planes along a axis, and the π electronic system of the bpy framework in [Pt(bpy){Co(d-pen)₂}]⁺ interacts with those in [Pt(bpy){Co(l-pen)₂}]⁺. Differences between the crystal structures of 2Cl · 3H₂O and3Cl · 7H₂O significantly reflect their diffuse reflectance spectra. In aqueous solution, each cation in both 2Cl · 3H₂O and 3Cl · 7H₂O is comparatively put on a free environment without such intermolecular interactions.     

Synthesis and structural characterizations of four polyoxometalate compounds consisting of transition metals or alkaline cations as the bridging units

Four new polyoxometalate compounds, namely [Cu₂(pyrazine)₄][Cu(pyrazine)₂][PMo₁₂O₄₀] · 2H₂O (1), {[K(H₂O)₂]₄H₈PW₁₂O₄₄}F · 8H₂O (2), H₉[K₂KMo₃₆O₁₁₂(H₂O)₃₄] · 35H₂O (3), and H₃Na₃[V₁₀O₂₈] · 15H₂O (4), were prepared and characterized by single crystal X-ray diffraction, elemental analysis and IR spectroscopy. Single crystal X-ray diffraction analysis results reveal that, in compound 1, Keggin anion of [PMoO₁₂O₄₀]³⁻ is enchased in the bowl-like Cu(I)-pyrazine intervals via weak interactions between terminal oxygen atoms and cations of Cu(I). For compound 2, a three-dimensional architecture with pores of 7.70 × 7.70 Å is constructed from the anions of [PW₁₂O₄₄]¹¹⁻ cross-linked via corner-sharing alkali cations of K⁺. The [Mo₃₆O₁₁₂(H₂O)₁₆]¹²⁻ units of compound 3 are linked to form one wave-like chain via cations of K⁺. Whereas, in compound 4, anions of [V₁₀O₂₈]³⁻ are linked via NaO₆ octahedra to form two-dimensional layer structure. On the basis of this two-dimensional layer, a three-dimensional architecture is further formed via hydrogen bonds involving edge-shared NaO₆ double octahedron.     

Two novel sandwiched-type polyoxotungstates containing Zn6 transition-metal cluster: Syntheses, structures and luminescent property

Two novel Zn6 sandwiched polyoxometalates, [Zn(phen)₂]₂[Zn₆(phen)₂(AsW₉O₃₃)₂] (1) and K₁₁H₂Zn[(ZnCl)₆(AsW₉O₃₃)₂]Cl · 27H₂O (2), have been synthesized and characterized by X-ray single-crystal analysis, IR, and fluorescence spectrum. The polyoxoanions in both compounds can be characterized as two {As^IIIW₉O₃₃}⁹⁻ moieties linked through Zn6 transition-metal cluster to form the sandwich-type polyoxotungstates. In compound 1, six Zn atoms in the equatorial part of the polyoxoanions have two different coordination environments: four Zn sites exhibit distorted octahedral geometry, and the other two Zn atoms show square pyramidal geometry. In the polyoxoanion of compound 2, all Zn atoms are square pyramidal geometry, and held together to form a hexagonal metallocycle by edge-sharing oxygen atoms. In this Zn6 cluster, the shortest distance of neighboring Zn?Zn is 3.147(1) Å. In addition, compound 2 exhibits purple photoluminescence at room temperature.     

Dioxouranium complexes as ligand. Synthesis and characterization of sandwich-type polyoxometalates [X2W18(UO2)2{(H2O)3M}2O68] (X = As and P) (M = Co, Cu, Mn, Ni and Zn)

The title complexes are synthesized by the reaction of an unusual ligand of [K₂P₂W₁₈(UO₂)₂O₆₈]¹²⁻ (1) and [KAs₂W₁₈(UO₂)₂O₆₈]¹³⁻ (2) with divalent metal ions of Co^II, Cu^II, Mn^II, Ni^II and Zn^II in 1:2 mole ratio and are characterized by elemental analysis, IR, ³¹P NMR, UV-Vis spectroscopy, TGA, and single crystal structure analysis. Crystals of [P₂W₁₈(UO₂)₂{(H₂O)₃Co}₂O₆₈]¹⁰⁻ (1a) and [As₂W₁₈(UO₂)₂{(H₂O)₃Cu}₂O₆₈]¹⁰⁻ (2b) are orthorhombic space group Cmca. Both 1a and 2b have structures in which two [M(H₂O)₃] (M = Co^II, Cu^II) and two UO₂ groups are sandwiched between two symmetry equivalent (XW₉) (X = P, As) units in a virtual C_i symmetry. In solution, 1a and [P₂W₁₈(UO₂)₂{(H₂O)₃Zn}₂O₆₈]¹⁰⁻ (1d) give two-line P NMR spectra that are consistent with a C_s symmetry structures so, are not consistent with the solid-state structures. The sodium salts of them give one-line P NMR spectra and are consistent with the C_i symmetry of solid-state structures. The uranium atoms have pentagonal-bipyramidal coordination, achieved by three equatorial bonds to the one XW₉ and two bonds to the other. The M atoms have octahedral or square pyramidal coordination, but only one bond to the one XW₉ and one bond to the other.     

Synthesis and spectroscopic properties of cobalt(III) complexes of some aroyl hydrazones: X-ray crystal structures of one cobalt(III) complex and two aroyl hydrazone ligands

Cobalt(III) complexes of diacetyl monooxime benzoyl hydrazone (dmoBH₂) and diacetyl monooxime isonicotinoyl hydrazone (dmoInH₂) have been synthesized and characterized by elemental analyses and spectroscopic methods. The X-ray crystal structures of the two hydrazone ligands, as well as that of the cobalt(III) complex [Co^III(dmoInH)₂]Cl·2H₂O, are also reported. It is found that in the cobalt(III) complexes the Co(III) ion is hexa-coordinated, the hydrazone ligands behaving as mono-anionic tridentate O,N,N donors. In the [Co^III(dmoInH)₂]Cl·2H₂O complex, the amide and the oxime hydrogens are deprotonated for both the ligands, while the isonicotine nitrogens are protonated. In the [Co^III(dmoBH)₂]Cl complex, only the amide nitrogens are deprotonated. It is shown that the additional hydrogen bonding capability of the isonicotine nitrogen results in different conformation and supramolecular structure for dmoInH₂, compared to dmoBH₂, in the solid state. Comparing the structure of the [Co^III(dmoInH)₂]Cl·2H₂O with that of the Zn(II) complex of the same ligand, reported earlier, it is seen that the metal ion has a profound influence on the supramolecular structure, due to change in geometrical dispositions of the chelate rings.     

Supramolecular salts containing the anionic [Ge(C2O4)3] complex and heteroaromatic amines

The crystalline compounds (Hbipy)₂[Ge(C₂O₄)₃] (1) and (Hphen)₂[Ge(C₂O₄)₃] · 2(H₂O) (2) [Hbipy⁺ is the 2,2′-bipyridinium cation (C₁₀H₉N₂), and Hphen⁺ is the 1,10′-phenathrolinium cation (C₁₂H₉N₂)] were isolated from mild hydrothermal syntheses and their structures were elucidated from single-crystal X-ray diffraction. The two compounds were further characterised by vibrational spectroscopy (FT-IR and FT-Raman), thermogravimetric analysis (TGA) and CHN elemental composition. Compounds 1 and 2 comprise the tris(oxalato-O,O′)germanate dianion complex, [Ge(C₂O₄)₃]²⁻, which co-crystallises with Hbipy⁺ (in 1), or Hphen⁺ and water molecules (in 2). In 1, the germanium oxalate anionic complex, [Ge(C₂O₄)₃]²⁻, and the Hbipy⁺ organic residues interact mutually via N-H?O hydrogen bonding interactions, leading to supramolecular discrete hydrogen-bonded units which are further interconnected via π-π stacking. Compound 2, on the other hand, exhibits a more complex hydrogen bonding network due to the presence of the water molecules of crystallisation which, along with π-π stacking between neighbouring Hphen⁺ residues, mediate the crystal packing.     

Selective synthesis of triangular cluster oxido-sulfidocomplexes of Mo and W: High yield preparations of [Mo3O2S2(H2O)9], [W3O2S2(H2O)9], [W2MoO2S2(H2O)9] and their derivatization

Reaction of [Mo₂O₂(μ-S)₂(H₂O)₆]²⁺ with Mo(CO)₆ or metallic Mo under hydrothermal conditions (140 °C, 4 M HCl) gives oxido-sulfido cluster aqua complex [Mo₃(μ₃-S)(μ-O)₂(μ-S)(H₂O)₉]⁴⁺ (1). Similarly, [W₃(μ₃-S)(μ-O)₂(μ-S)(H₂O)₉]⁴⁺ (2) is obtained from [W₂O₂(μ-S)₂(H₂O)₆]²⁺ and W(CO)₆. While reaction of [Mo₂O₂(μ-S)₂(H₂O)₆]²⁺ with W(CO)₆ mainly proceeds as simple reduction to give 1, [W₂O₂(μ-S)₂(H₂O)₆]²⁺ with Mo(CO)₆ produces new mixed-metal cluster [W₂Mo(μ₃-S)(μ-O)₂(μ-S)(H₂O)₉]⁴⁺ (3) as main product. From solutions of 1 in HCl supramolecular adduct with cucurbit[6]uril (CB[6]) {[Mo₃O₂S₂(H₂O)₆Cl₃]₂CB[6]}Cl₂⋅18H₂O (4) was isolated and structurally characterized. The aqua complexes were converted into acetylacetonates [M₃O₂S₂(acac)₃(py)₃]PF₆ (M₃ = Mo₃, W₃, W₂Mo; 5a-c), which were characterized by X-ray single crystal analysis, electrospray ionization mass spectrometry and ¹H NMR spectroscopy. Crystal structure of (H₅O₂)(Me₄N)₄[W₃(μ₃-S)(μ₂-S)(μ₂-O)₂(NCS)₉] (6), obtained from 2, is also reported.     

Two dumbbell-like polyoxometalates constructed from capped molybdovanadate and transition metal complexes

Self assembly of NaVO₃, Na₂MoO₄·2H₂O and NiCl₂·6H₂O with the assistance of organic liginds under hydrothermal conditions results in two molybdovanadates [Ni(enMe)₂]₄{[Ni(enMe)₂(H₂O)]₂[Ni(enMe)₂][(V^VMo^VI₈V₄^IVO₄₀)(V^IVO)₂]₂}·10H₂O (1) and [Ni(enMe)₂]₅{[Ni(enMe)₂]₂[(V^VMo^VI₄Mo^V₄V₄^IVO₄₀)(V^IVO)₄]₂}·2H₂O (2), (enMe = 1,2-diaminopropane), which have been characterized by single crystal X-ray diffraction analysis, IR spectroscopy, and elemental analysis. Both of the two compounds exhibit dumbbell-like structures constructed from capped polyoxomolybdovanadates and [Ni(enMe)₂]²⁺ complexes. Polyoxoxanion 1 is composed of two bicapped Keggin-type anions [(V^VMo₈V₄^IVO₄₀)(V^IVO)₂]⁷⁻, one [Ni(enMe)₂]²⁺ bridging fragment and two decorated nickel(II) complexes. Polyxoxanion 2 consists of two tetracapped molybdenum-vanadium polyoxoanions [(V^VMo^VI₄Mo^V₄V₄^IVO₄₀)(V^IVO)₄]⁷⁻, one [Ni(enMe)₂]²⁺ bridging fragment and a nickel(II) decorated fragment. Polyxoxanions 1 and 2 are further linked to form three-dimensional supramolecular networks through extensive hydrogen bonding interactions. In addition, photocatalysis properties of these two compounds have been investigated.     

Cyano-bridged cluster-metal coordination compound: synthesis and crystal structure of [Cu(NH3)3][Cu(NH3)4][Cu(NH3)5][W4Te4(CN)12]·5H2O

Dark-brown single crystals of the title compound 1 were obtained in high yield by layering a CuCl₂ solution in 25% aqueous ammonia on a glycerol solution of K₆[W₄Te₄(CN)₁₂]·5H₂O. The complex 1 was characterized by single crystal X-ray diffraction analysis and IR spectroscopy. The X-ray structure of 1 reveals a polymeric chain cyano-bridged cluster-metal coordination compound. The [W₄Te₄(CN)₁₂]⁶⁻ cluster anions are linked one to another by Cu²⁺ cations through coordination by nitrogen atoms of the CN groups.     

Two Cd(II) and Ni(II) complexes constructed with dicyanamide and picolinate ligands

Two new dianion metal-organic complexes {[Cd(pcl)(H₂O)₂]₂[Cd(pcl)₂(dca)₂]} (1) and [Ni(pcl)(dca)(H₂O)]₂ (2) (dca = dicyanamide, Hpcl = picolinic acid) have been synthesized and characterized by IR spectra and X-ray diffraction. In complex 1, the pcl⁻ ligand both acts as chelate and bridging coordination ligands, while in complex 2, which only acts as a chelate ligand. In both cases, μ-1, 5-dca ligands bridge the metal ions to form square-grid like [M(dca)₂]₂ dimers. In complex 1, four of the trinuclear second building units {[Cd(pcl)(H₂O)₂]₂[Cd(pcl)₂(dca)₂]} formed a honeycomb-like cavity, which further bridged by pcl⁻ and dca to give a 2D network. While in complex 2, a channel-like supramolecular structure is formed by the connection of numerous hydrogen-bond interactions and weak interactions among the dinuclear motifs. Thermally gravimetric analyses and differential thermal analyses indicate that the two complexes are thermal stable.