Extended polyoxometalate framework solids: two Mn(II)-linked {P8W48} network arrays

Two polyoxometalate open framework (POMOF) materials have been synthesized using a secondary building unit (SBU) approach that facilitates the convergent assembly of multidimensional framework materials using a preassembled anionic SBU {P(8)W(48)}, with integrated "pore" 1 nm in diameter, and electrophilic manganese {Mn(2+)} linkers. This yields two new POMOFS with augmented hexagonal tiling (2 and 3), related to a known three-dimensional (3D) cubic array K(18)Li(6)[Mn(II)(8)(H(2)O)(48)P(8)W(48)O(184)]·108H(2)O (1), K(12)[Mn(II)(14)(H(2)O)(30)P(8)W(48)O(184)]·111H(2)O (2), and K(8)Li(4)[Mn(II)(14)(H(2)O)(26)P(8)W(48)O(184)]·105H(2)O (3). These frameworks have been crystallized from aqueous Li-buffered solutions of {P(8)W(48)} and Mn(II)(ClO(4))(2)·6H(2)O via careful control of the synthetic strategy akin to a crystal engineering approach using cation and temperature control to isolate different material architectures shown by compounds 1-3.     

Organoruthenium derivative of the cyclic [H7P8W48O184]33- anion: [{K(H2O)}3{Ru(p-cymene)(H2O)}4P8W49O186(H2O)2]27-

Reaction of [Ru(p-cymene)Cl2]2 with [H7P8W48O184]33- (P8W48) in aqueous acidic medium results in the organometallic derivative [{K(H2O)}3{Ru(p-cymene)(H2O)}4P8W49O186(H2O)2]27- (1); in addition to the four {Ru(p-cymene)(H2O)} units, an unusual WO6 group with four equatorial, terminal ligands is also grafted to the crown-shaped P8W48 precursor.     

Molecular and multidimensional polyoxotungstates functionalized by {Cu(bpy)}2+ groups

Five new materials built from polyoxotungstates and Cu(ii) ions as linkers have been synthesized by hydrothermal reactions from a mixture of sodium tungstate, copper chloride and bipyridine. The value of the initial pH, the nature of the heteroelement (P or Si) and of the ligand (2,2'- and/or 4,4'-bipyridine) permit the control of the nature of the polyoxotungstate clusters and their connectivity via the copper ions, and hence the dimensionality of the framework. A single phase has been obtained with silicon as heteroelement at an initial pH of 5, namely the 2D material [SiW(12)O(40)][Cu(2,2'-bpy)(2)](2).10H(2)O (1) with saturated Keggin polyoxotungstates linked by {Cu(2,2'-bpy)(2)}(2+) groups. With phosphorous as heteroelement and at the same initial pH, three different structures have been isolated according to the nature of the ligand. Indeed, the two 1D materials [{Cu(5)(2,2'-bpy)(5)(H(2)O)(HPO(4))(PO(4))}PW(11)CuO(39)].6H(2)O (2) with 2,2'-bpy and [4,4'-Hbpy][{Cu(2)(2,2'-bpy)(2)(4,4'-bpy)(2.5)}PW(11)CuO(39)].16H(2)O (3) with a mixture of 2,2'- and 4,4'-bpy have been characterized, and a coordination polymer with polyoxometalate guests Na(3)[4,4'-Hbpy]{Cu(4)(4,4'-bpy)(8)(H(2)O)(8)}[PW(11)CuO(39)(H(2)O)][PW(10)Cu(2)O(38)(H(2)O)(2)].38H(2)O (4) with 4,4'-bpy has been obtained. Finally, in basic medium (pH = 10) the unprecedented molecular cluster Na(2)[{Cu(8)(2,2'-bpy)(8)}(PW(8)O(31))(2)].15H(2)O (5) has been evidenced. Magnetic studies of compound 2 revealed that the predominant interactions involve only 4 paramagnetic centers, which are interacting within pairs, among the 6 Cu(ii) centers. The chi(M)T=f(T) curve can be fitted using the dinuclear expression appropriate to the HDVV isotropic exchange Hamiltonian H=-JS(1)xS(2), with S(1)=S(2)=(1/2) and J=-105.4 cm(-1), showing strong antiferromagnetic interactions within the two Cu(ii) pairs.     

Characterization and electrochemical properties of molecular icosanuclear and bidimensional hexanuclear Cu(II) azido polyoxometalates

Two new Cu(II) azido polyoxometalates compounds have been synthesized, and their structures were determined by X-ray crystallography. The compound Na(14)[SiW(9)O(34)Cu(3)(N(3))(2)(OH)(H(2)O)](2) x 24H(2)O (1) is built from two [SiW(9)O(34)Cu(3)(mu(1,1,3)-N(3))(2)(mu-OH)(H(2)O)](7-) subunits where the copper centers, connected by two azido ligands and one hydroxo group, form a nearly equilateral triangle. The two subunits are related by an inversion center and connected via the two mu(1,1,3)-N(3) ligands in an end-to-end fashion, affording a hexanuclear Cu(II) cluster. Linkage of these fragments via Cu-O=W bonds leads to a bidimensional arrangement of the polyoxometalate units. The complex LiK(14)Na(9)[P(8)W(48)O(184)Cu(20)(N(3))(6)(OH)(18)] x 60H(2)O (2) consists of two {Cu(5)(OH)(4)}(6+) and two {Cu(5)(OH)(2)(mu(1,1,3,3)-N(3))}(7+) subunits connected via four mu-OH and four mu(1,1)-N(3) additional ligands, the 20 copper centers being encapsulated in the [P(8)W(48)O(184)](40-) crown polyoxotungstate ligand. 1 represents the first multidimensional compound based on azido polyoxometalate (POM) units, and 2 represents by far the largest azido POM complex isolated to date. Magnetic measurements revealed an overall antiferromagnetic behavior for both compounds. Nevertheless, the study of the variation of the magnetization with the applied field indicates that 1 possesses a triplet ground state, which can be attributed to weak ferromagnetic interaction between the S = 1/2 triangular subunits. The stability of 1 and 2 evidenced by UV-vis spectroscopy and gel filtration chromatography, in particular at pH 5, has allowed a detailed study of their redox and electrocatalytic properties. For both compounds, the stability of the Cu(II)/Cu(I) couple is remarkable compared with the observations made in other Cu(II)-substituted POMs. Electrochemical quartz crystal microbalance measurements clearly demonstrate that the formation of the Cu(I) species occurs neatly without the formation of Cu(0). The accumulation of such Cu(II) centers within the complexes is a favorable condition to envision applications involving several electrons. The electrocatalytic reduction of dioxygen and hydrogen peroxide was achieved efficiently and has shown that the reactivity increases with the nuclearity and/or the Cu/W ratio of the POM complex. The dioxygen reduction is an overall four-electron process with water as the final product. Finally, the reduction of the W centers triggers a strong electrocatalysis of solvent reduction.     

Novel polyoxometalate hybrids consisting of copper-lanthanide heterometallic/lanthanide germanotungstate fragments

Three organic-inorganic hybrid copper-lanthanide heterometallic germanotungstates, {[Cu(en)(2)(H(2)O)] [Cu(3)Eu(en)(3)(OH)(3)(H(2)O)(2)](α-GeW(11)O(39))}(2)·11H(2)O (1), {[Cu(en)(2)(H(2)O)][Cu(3)Tb(en)(3)(OH)(3)(H(2)O)(2)](α-GeW(11)O(39))}(2)·11H(2)O (2) and {[Cu(en)(2)(H(2)O)][Cu(3)Dy(en)(3)(OH)(3)(H(2)O)(2)](α-GeW(11)O(39))}(2)·10H(2)O (3) and three polyoxometalate hybrids built by lanthanide-containing germanotungstates and copper-ethylendiamine complexes, Na(2)H(6)[Cu(en)(2)(H(2)O)](8){Cu(en)(2)[La(α-GeW(11)O(39))(2)](2)}·18H(2)O (4), K(4)H(2)[Cu(en)(2)(H(2)O)(2)](5)[Cu(en)(2)(H(2)O)](2)[Cu(en)(2)](2){Cu(en)(2)[Pr(α-GeW(11)O(39))(2)](2)}·16H(2)O (5) and KNa(2)H(7)[enH(2)](3)[Cu(en)(2)(H(2)O)](2)[Cu(en)(2)](2){Cu(en)(2)[Er(α-GeW(11)O(39))(2)](2)}·15H(2)O (6) (en = ethylenediamine) have been hydrothermally synthesized and structurally characterized by elemental analyses, inductively coupled plasma atomic emission spectrometry (ICP-AES) analyses, IR spectra, powder X-ray diffraction (PXRD), X-ray photoelectron spectroscopy (XPS) and single-crystal X-ray diffraction. 1-3 are essentially isomorphous and their main skeletons display the interesting dimeric motif {[Cu(3)Ln(en)(3)(OH)(3)(H(2)O)(2)](α-GeW(11)O(39))}(2)(4-), which is constructed from two {Cu(3)LnO(4)} cubane anchored monovacant [α-GeW(11)O(39)](8-) fragments through two W-O-Ln-O-W linkers. The primary backbones of 4-6 exhibit the tetrameric architecture {Cu(en)(2)[Ln(α-GeW(11)O(39))(2)](2)}(24-) built by two 1?:?2-type [Ln(α-GeW(11)O(39))(2)](13-) moieties and one [Cu(en)(2)](2+) bridge, albeit they are not isostructural. To our knowledge, 1-6 are rare polyoxometalate derivatives consisting of copper-lanthanide heterometallic/lanthanide germanotungstate fragments. 1 exhibits antiferromagnetic coupling interactions within the {Cu(3)EuO(4)} cubane units, while 2 and 3 display dominant ferromagnetic interactions between the Tb(III)/Dy(III) and Cu(II) cations. The room-temperature solid-state photoluminescence properties of 1-3 have been investigated.     

Microwave-assisted construction of ferromagnetic coordination polymers of [W(V)(CN)8]3- with Cu(II)-pyrazole synthons

The microwave-mediated self-assembly of [W(V)(CN)(8)](3-) with Cu(II) in the presence of pyrazole ligand resulted in the formation of three novel assemblies: Cu(II)(2)(Hpyr)(5)(H(2)O)[W(V)(CN)(8)](NO(3))·H(2)O (1), {Cu(II)(5)(Hpyr)(18)[W(V)(CN)(8)](4)}·[Cu(II)(Hpyr)(4)(H(2)O)(2)]·9H(2)O (2), and Cu(II)(4)(Hpyr)(10)(H(2)O)[W(V)(CN)(8)](2)(HCOO)(2)·4.5H(2)O (3) (Hpyr =1H-pyrazole). Single-crystal X-ray structure of 1 consists of cyanido-bridged 1-D chains of vertex-sharing squares topology. The structure of 2 reveals 2-D hybrid inorganic layer topology with large coordination spaces occupied by {Cu(Hpyr)(2)(H(2)O)(4)}(2+) ions. Compound 3 contains two types of cyanido-bridged 1-D chains of vertex-sharing squares linked together by formate ions in two directions forming hybrid inorganic-organic 3-D framework (I(1)O(2)). The magnetic measurements for 1-3 reveal a weak ferromagnetic coupling through Cu(II)-NC-W(V) bridges.     

Oxothiomolybdenum derivatives of the superlacunary crown heteropolyanion {P8W48}: structure of [K4{Mo4O4S4(H2O)3(OH)2}2(WO2)(P8W48O184)]30– and studies in solution

Reaction of the cyclic lacunary [H(7)P(8)W(48)O(184)](33-) anion (noted P(8)W(48)) with the [Mo(2)S(2)O(2)(H(2)O)(6)](2+) oxothiocation led to two compounds, namely, [K(4){Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2)(WO(2))(P(8)W(48)O(184))](30-) (denoted 1) and [{Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2)(P(8)W(48)O(184))](36-) (denoted 2), which were characterized in the solid state and solution. In the solid state, the structure of [K(4){Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2)(WO(2))(P(8)W(48)O(184))](30-) reveals the presence of two disordered {Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2+) "handles" connected on both sides of the P(8)W(48) ring. Such a disorder is consistent with the presence of two geometrical isomers where the relative disposition of the two {Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2+) handles are arranged in a perpendicular or parallel mode. Such an interpretation is fully supported by (31)P and (183)W NMR solution studies. The relative stability of both geometrical isomers appears to be dependent upon the nature of the internal alkali cations, i.e., Na(+) vs K(+), and increased lability of the two {Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2+) handles, compared to the oxo analogous, was clearly identified by significant broadening of the (31)P and (183)W NMR lines. Solution studies carried out by UV-vis spectroscopy showed that formation of the adduct [{Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2)(P(8)W(48)O(184))](36-) occurs in the 1.5-4.7 pH range and corresponds to a fast and quantitative condensation process. Furthermore, (31)P NMR titrations in solution reveal formation of the "monohandle" derivative [{Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(P(8)W(48)O(184))](38-) as an intermediate prior to formation of the "bishandle" derivatives. Furthermore, the electrochemical behavior of [{Mo(4)O(4)S(4)(H(2)O)(3)(OH)(2)}(2)(P(8)W(48)O(184))](36-) was studied in aqueous medium and compared with the parent anion P(8)W(48).     

Synthesis, Structure and Characterization of [Cu(2,2''-bpy)2][{Cu(2,2''-bpy)2}2W12O40(H2)]·4H2O

An organic-inorganic compound [Cu(2,2'-bpy)2][{Cu(2,2'-bpy)2}2W12O4o(H2)]·4H2O (Mr = 4048.00) was prepared from the hydrothermal reaction of Na2WO4·2H2O, CuCl2·2H2O,2,2'-bipyridine (2,2'-bpy) and H2O at 160 ℃ for 4 days. The compound crystallizes in the monoclinic system, space group P21/n with a = 18.9196(8), b = 20.4212(8), c = 21.8129(9)(A), β=96.992(3)°, V= 8365.0(6) (A)3, Dc= 3.214 g/cm3, Z = 4,μ(MoKα) = 17.269 mm-1 and F(000) = 7324.Of the 119837 total reflections, 17315 were unique (Rint = 0.0489). The final R = 0.0385 and wR =0.0770 for 11142 observed reflections with I ＞ 2σ(I). Single-crystal X-ray diffraction reveals that the structure is composed of [{Cu(2,2'-bpy)2}2W12O40(H2)]2- anions, discrete [Cu(2,2'-bpy)2]2 cations and lattice water molecules, and the anion is made up of a {W12O40(H2)}6- α-Keggin core decorated with two {Cu(2,2'-bpy)2}2 groups through bridging oxygen atoms.     

Di- and tricobalt Dawson sandwich complexes: synthesis,spectroscopic characterization,and electrochemical behavior of Na(18)[(NaOH(2))(2)Co(2)(P(2)W(15)O(56))(2)] and Na(17)[(NaOH(2))Co(3)(H(2)O)(P(2)W(15)O(56))(2)

The reaction of the trivacant Dawson anion alpha-[P(2)W(15)O(56)](12-) and the divalent cations Co(2+) is known to form the tetracobalt sandwich complex [Co(4)(H(2)O)(2)(P(2)W(15)O(56))(2)](16-) (Co(4)P(4)W(30)). Two new complexes, with different Co/P(2)W(15) stoichiometry, [(NaOH(2))(2)Co(2)(P(2)W(15)O(56))(2)](18-) (Na(2)Co(2)P(4)W(30)) and [(NaOH(2))Co(3)(H(2)O)(P(2)W(15)O(56))(2)](17-) (NaCo(3)P(4)W(30)), have been synthesized as aqueous-soluble sodium salts, by a slight modification of the reaction conditions. Both compounds were characterized by IR, elemental analysis, and (31)P solution NMR spectroscopy. These species are "lacunary" sandwich complexes, which add Co(2+) cations according to Na(2)Co(2)P(4)W(30) + Co(2+) --> NaCo(3)P(4)W(30) + Na(+) followed by NaCo(3)P(4)W(30) + Co(2+) --> Co(4)P(4)W(30) + Na(+). A Li(+)/Na(+) exchange in the cavity was evidenced by (31)P dynamic NMR spectroscopy. The electrochemical behaviors of the sandwich complexes [(NaOH(2))Co(3)(H(2)O)(P(2)W(15)O(56))(2)](17-) and [(NaOH(2))(2)Co(2)(P(2)W(15)O(56))(2)](18-) were investigated in aqueous solutions and compared with that of [Co(4)(H(2)O)(2)(P(2)W(15)O(56))(2)](16-). These complexes showed an electrocatalytic effect on nitrite reduction.     

New class of Preyssler-lanthanide complexes with modified and extended structures tuned by the lanthanide contraction effect

A family of polyoxometalate compounds based on Preyssler anions and lanthanide cations, K(5)Na(5)[{Pr(4)(H(2)O)(12)(pydc)(4)}{Na(H(2)O)P(5)W(30)O(110)}]·46H(2)O (1, H(2)pydc = pyridine-2,6-dicarboxylic acid), Na(7)[{Pr(4)(H(2)O)(20)(pydc)(2)(Ac)}{Na(H(2)O)P(5)W(30)O(110)}]·23H(2)O (2), and Na(10)H(2) [{Ln(2)(H(2)O)(10)(pydc)(2)}{Na(H(2)O)P(5)W(30)O(110)}]·XH(2)O (Ln = Sm 3, Eu 4, Gd 5; X = 11 for 3 and 5, 13 for 4), have been synthesized and characterized by elemental analysis and single crystal X-ray diffraction. Compound 1 exhibits a two-dimensional honeycomb layer which is built up from unique {Pr(4)} metallacycles and Preyssler anions. Remarkably, the strong involvement of the sodium countercations leads to the formation of a unique three-dimensional open architecture with one-dimensional channels. The 2D grid layer of compound 2 is constructed by the longest currently known rare-earth metal clusters {Pr(8)} and Preyssler anions. Isostructural compounds 3, 4, and 5, obtained by introduction of the intermediate lanthanide ions into the above reaction system, exhibit bisupporting [{Ln(2)(H(2)O)(10)(pydc)(2)}{Na(H(2)O)P(5)W(30)O(110)}](12-) polyoxometalate cluster structures. The magnetic properties of compounds 1 and 2 and the luminescent properties of compounds 3 and 4 are discussed in this paper.     

Photochromic hybrid materials of cucurbituril and polyoxometalates as photocatalysts under visible light

Two isostructural organic-inorganic hybrid solid materials based on cucurbituril derivatives and polyoxometalates, {[K(2)(H(2)O)(2)Na(2)(H(2)O)(2)Na(2)(H(2)O)(6)](P(2)W(18)O(62))(Me(10)Q(5))(2)}·~7H(2)O (1) and {[Rb(2)(H(2)O)(2)Na(2)(H(2)O)Na(2)(H(2)O)(4)](P(2)W(18)O(62))(Me(10)Q(5))(2)}·~8H(2)O (2), which exhibit reversible photochromic properties as well as excellent photocatalytic activities toward the degradation of methyl orange (MO) and rhodamine-B (RB) under visible light irradiation, are reported.     

Selective inclusion of Cu+ and Ag+ electron-rich metallic cations within supramolecular polyoxometalates based on {AsW9O33}{Mo3S4} combinations

Coordination of the [Mo(3)S(4)(H(2)O)(9)](4+) cluster with the trivacant [AsW(9)O(33)](9-) ion gives the supramolecular complex [{(H(4)AsW(9)O(33))(4)(Mo(3)S(4){H(2)O}(5))}(2)](12-) (1) in good yield. The structure of 1 shows that two [H(4)AsW(9)O(33)](5-) subunits sandwich a single central [Mo(3)S(4)(H(2)O)(5)](4+) ion to give a basic monomeric unit [(H(4)AsW(9)O(33))(2){Mo(3)S(4)(H(2)O)(5)}](6-). In the solid state, a supramolecular dimeric association is evidenced that consists of two [(H(4)AsW(9)O(33))(2){Mo(3)S(4)(H(2)O)(5)}](6-) units held together by twelve hydrogen bonds and four SS contacts. Complex 1 reacts with NaAsO(2), AgNO(3) and CuI to give compounds 2, 3 and 4, respectively. X-ray structural analysis reveals that the molecular arrangements of 2 to 4 are closely related to the parent structure of 1. {AsOH}(2+), Ag(+) and Cu(+) ions are located on three distinct pairs of sites. Two hanging {AsOH}(2+) groups in 2 are symmetrically attached to two opposite {AsW(9)O(33)} subunits. Complex 3 is the first example of an Ag/{Mo(3)S(4)} combination in which the environment of the two equivalent Ag(+) cations is remarkable for containing two sulfur atoms belonging to {Mo(3)S(4)}, two oxygen and one central arsenic atom of the {AsW(9)O(33)} subunits. Potentiometric titration shows that the addition of Ag(+) ions is quantitative and occurs in two successive steps (K(1)=4.1 x 10(6) and K(2)=2.3 x 10(5) L mol(-1)), which is consistent with the retention of the supramolecular cluster in solution. The structure of 4 reveals a single copper atom embedded in the central part of the dimer. The Cu(+) cation is bound to four sulfur atoms to complete a cuboidal moiety. UV/Vis studies in solution indicate that the stability of the dimeric assemblies of 2, 3 and 4 is significantly enhanced by the presence of Cu(+) or Ag(+) ions, which act as additional coordination linkers within the supramolecular cluster. The anions 1 to 4 were characterised by (183)W NMR spectroscopy in solution. The 10-line spectra recorded for each of them are consistent with an averaged C(2h) molecular symmetry in solution.     

3d-Metal derivatives of the [Cu(I)(SO3)4]7- ion: structure and magnetism

The Cu(SO(3))(4)(7-) anion, which consists of a tetrahedrally coordinated Cu(I) centre coordinated to four sulfur atoms, is able to act as a multidentate ligand in discrete and infinite supramolecular species. The slow oxidation of an aqueous solution of Na(7)Cu(SO(3))(4) yields a mixed oxidation state, 2D network of composition Na(5){[Cu(II)(H(2)O)][Cu(I)(SO(3))(4)]}·6H(2)O. The addition of Cu(II) and 2,2'-bipyridine to an aqueous Na(7)Cu(SO(3))(4) solution leads to the formation of a pentanuclear complex of composition {[Cu(II)(H(2)O)(bipy)](4)[Cu(I)(SO(3))(4)]}(+); a combination of hydrogen bonding and π-π stacking interactions leads to the generation of infinite parallel channels that are occupied by disordered nitrate anions and water molecules. A pair of Cu(SO(3))(4)(7-) anions each act as a tridentate ligand towards a single Mn(II) centre when Mn(II) ions are combined with an excess of Cu(SO(3))(4)(7-). An anionic pentanuclear complex of composition {[Cu(I)(SO(3))(4)](2)[Fe(III)(H(2)O)](3)(O)} is formed when Fe(II) is added to a Cu(+)/SO(3)(2-) solution. Hydrated ferrous [Fe(H(2)O)(6)(2+)] and sodium ions act as counterions for the complexes and are responsible for the formation of an extensive hydrogen bond network within the crystal. Magnetic susceptibility studies over the temperature range 2-300 K show that weak ferromagnetic coupling occurs within the Cu(II) containing chains of Na(5){[Cu(II)(H(2)O)][Cu(I)(SO(3))(4)]}·6H(2)O, while zero coupling exists in the pentanuclear cluster {[Cu(II)(H(2)O)(bipy)](4)[Cu(I)(SO(3))(4)]}(NO(3))·H(2)O. Weak Mn(II)-O-S-O-Mn(II) antiferromagnetic coupling occurs in Na(H(2)O)(6){[Cu(I)(SO(3))(4)][Mn(II)(H(2)O)(2)](3)}, the latter formed when Mn was in excess during synthesis. The compound, Na(3)(H(2)O)(6)[Fe(II)(H(2)O)(6)](2){[Cu(I)(SO(3))(4)](2)[Fe(III)(H(2)O)](3)(O)}·H(2)O, contained trace magnetic impurities that affected the expected magnetic behaviour.     

Coordination site-dependent cation binding and multi-responsible redox properties of Janus-head metalloligand, [Mo(V)(1,2-mercaptophenolato)3

The redox-active fac-[Mo(V)(mp)(3)](-) (mp: o-mercaptophenolato) bearing asymmetric O- and S-cation binding sites can bind with several kinds of metal ions such as Na(+), Mn(II), Fe(II), Co(II), Ni(II), and Cu(I). The fac-[Mo(V)(mp)(3)](-) metalloligand coordinates to Na(+) to form the contact ion pair {Na(+)(THF)(3)[fac-Mo(V)(mp)(3)]} (1), while a separated ion pair, n-Bu(4)N[fac-Mo(V)(mp)(3)] (2), is obtained by exchanging Na(+) with n-Bu(4)N(+). In the presence of asymmetric binding-sites, the metalloligand reacts with Mn(II)Cl(2)·4H(2)O, Fe(II)Cl(2)·4H(2)O, Co(II)Cl(2)·6H(2)O, and Ni(II)Cl(2)·6H(2)O to afford UV-vis-NIR spectra, indicating binding of these guest metal cations. Especially, for the cases of the Mn(II) and Co(II) products, trinuclear complexes, {M(H(2)O)(MeOH)[fac-Mo(V)(mp)(3)](2)}·1.5CH(2)Cl(2) (3·1.5CH(2)Cl(2) (M = Mn(II)), 4·1.5CH(2)Cl(2) (M = Co(II))), are successfully isolated and structurally characterized where the M are selectively bound to the hard O-binding sites of the fac-[Mo(V)(mp)(3)](-). On the other hand, a coordination polymer, {Cu(I)(CH(3)CN)[mer-Mo(V)(mp)(3)]}(n) (5), is obtained by the reaction of fac-[Mo(V)(mp)(3)](-) with [Cu(I)(CH(3)CN)(4)]ClO(4). In sharp contrast to the cases of 1, 3·1.5CH(2)Cl(2), and 4·1.5CH(2)Cl(2), the Cu(I) in 5 are selectively bound to the soft S-binding sites, where each Cu(I) is shared by two [Mo(V)(mp)(3)](-) with bidentate or monodentate coordination modes. The second notable feature of 5 is found in the geometric change of the [Mo(V)(mp)(3)](-), where the original fac-form of 1 is isomerized to the mer-[Mo(V)(mp)(3)](-) in 5, which was structurally and spectroscopically characterized for the first time. Such isomerization demonstrates the structural flexibility of the [Mo(V)(mp)(3)](-). Spectroscopic studies strongly indicate that the association/dissociation between the guest metal ions and metalloligand can be modulated by solvent polarity. Furthermore, it was also found that such association/dissociation features are significantly influenced by coexisting anions such as ClO(4)(-) or B(C(6)F(5))(4)(-). This suggests that coordination bonds between the guest metal ions and metalloligand are not too static, but are sufficiently moderate to be responsive to external environments. Moreover, electrochemical data of 1 and 3·1.5CH(2)Cl(2) demonstrated that guest metal ion binding led to enhance electron-accepting properties of the metalloligand. Our results illustrate the use of a redox-active chalcogenolato complex with a simple mononuclear structure as a multifunctional metalloligand that is responsive to chemical and electrochemical stimuli.     

Structures and magnetism of {Ni2Na2}, {Ni4} and {Ni6(II)Ni(III)} 2-hydroxy-3-alkoxy-benzaldehyde clusters

Three polynuclear complexes, [NiNa(μ(1,1,1)-N(3))(μ-hmb)(2)(DMF)](2), (1), [Ni(4)(μ(3)-OMe)(4)(heb)(4)(MeOH)(1.05)(H(2)O)(2.95)], (2) and [Ni(III)(OH)(6)(hmb)(6)Ni(II)(6)]·(ClO(4))(3) (3) (Hhmb = 2-hydroxy-3-methoxy-benzaldehyde; Hheb = 2-hydroxy-3-ethoxy-benzaldehyde), were prepared by reaction of the appropriate ligand with nickel(II) perchloride hexahydrate under solvothermal conditions. All compounds were characterized by elemental analysis, IR spectroscopy and X-ray single-crystal diffraction. Compound 1 exhibits a centrosymmetric heterotetranuclear cluster which represents the first nickel complex to possess two connected face-sharing cubes structure {Ni(2)Na(2)N(2)O(4)}. Compound 2 has a tetranuclear Ni cluster with a cubane topology in which the Ni(II) and the oxygen atoms from the methanol ligands occupying alternate vertices of the cube. Compound 3 consisits of a mixed-valence [Ni(III)(OH)(6)(hmb)(6)Ni(II)(6)](3+) subunits and it represents the first nickel {Ni(II)(6)Ni(III)} complex to possess a planar hexagonal disc-like structure. The results show that the minor ligand modifications or solvent change have a key role in the structural control of the self-assembly process. Magnetic properties of 1-3 in the 300-2 K have been discussed. The {Ni(2)Na(2)} (1) and {Ni(4)} (2) core display dominant ferromagnetic interactions from the nature of the binding modes through μ(3)-N(3)(-) or μ(3)-OCH(3)(-), while {Ni(II)(6)Ni(III)} core (3) displays dominant anti-ferromagnetic interactions from the nature of the binding modes through μ(3)-OH(-).     

Self-assembly and photocatalytic properties of polyoxoniobates: {nb(24)o(72)}, {nb(32)o(96)}, and {k(12)nb(96)o(288)} clusters

Three novel polyoxoniobates, KNa(2)[Nb(24)O(72)H(21)]·38H(2)O (1), K(2)Na(2)[Nb(32)O(96)H(28)]·80H(2)O (2), and K(12)[Nb(24)O(72)H(21)](4)·107H(2)O (3) with molecular triangle, molecular square, and cuboctahedral molecular cage geometries, respectively, have been successfully synthesized by conventional aqueous methods. All the compounds are built from [Nb(7)O(22)](9-) fundamental building units. Compound 1 is the first isolated {Nb(24)O(72)} cluster, featuring three heptaniobate clusters linked in a ring by three additional NbO(6) octahedra, while compound 2 is the largest isopolyoxoniobate cluster reported to date, consisting of four heptaniobate clusters linked by four additional NbO(6) octahedra. Compound 3 is the largest solid aggregation of polyoxoniobates, assembled by four {KNb(24)O(72)} clusters joined by four K ions. To our knowledge, it is the first time these polyoxoniobate clusters have been crystallized with only alkali-metal counterions, thereby giving them the possibility of being redissolved in water. ESI-MS spectra indicate that compounds 1 and 2 remain structural integrity when the pure, crystalline polyanion salts are dissolved in water, while compound 3 is partially assembled into Nb(24) fragments. The UV-vis diffuse reflectance spectra of these powder samples indicate that the corresponding well-defined optical absorption associated with E(g) can be assessed at 3.35, 3.17, and 3.34 eV, respectively, revealing the presence of an optical band gap and the nature of semiconductivity with a wide band gap. UV-light photocatalytic H(2) evolution activities were observed for these compounds with Co(III)(dmgH)(2)pyCl as a cocatalyst and TEA as a sacrificial electron donor.     

A series of vanadogermanates from 1D chain to 3D framework built by Ge-V-O clusters and transition-metal-complex bridges

Three novel extended vanadogermanates, {[(en)(2)Cd(2)Ge(8)V(12)O(40)(OH)(8)(H(2)O)][Cd(en)(2)](2)}·6H(2)O (1), {[Zn(2)(dap)(3)][Zn(dap)](2)Ge(6)V(15)O(48)(H(2)O)}[Zn(dap)(2)(H(2)O)](2)·3H(2)O (2), and {[Cd(3)(μ-dien)(2)(Hdien)(2)(H(2)O)(2)]Ge(4)V(16)O(42)(OH)(4)(H(2)O)}·2H(2)O (3; en=ethylenediamine, dap=1,2-diaminopropane, dien=diethylenetriamine), have been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectroscopy, powder XRD, thermogravimetric analysis, and single-crystal XRD. Their Ge-V-O cluster anions are derived from the V(18)O(42) cluster shell by replacing VO(5) square pyramids with Ge(2)O(7) groups. Compound 1 exhibits a 1D sinusoidal chain built up from rare inorganic-organic hybrid dicadmium-substituted vanadogermanate {[Cd(en)](2)V(12)O(40)(GeOH)(8)(H(2)O)} clusters and [Cd(en)(2)] complexes. Compound 2 is the first example of a 2D network based on linkage of the unusual {Ge(6)V(15)O(48)(H(2)O)} clusters and two types of Zn complex fragments. Compound 3 is an unprecedented 3D framework built by {Ge(4)V(16)O(42)(OH)(4)(H(2)O)} clusters and rare trinuclear bridging complex cations [Cd(3)(μ-dien)(2)(Hdien)(2)(H(2)O)(2)](8+). Magnetic measurements illustrate that both 1 and 2 have antiferromagnetic exchange interactions between metal centers, whereas 3 exhibits ferrimagnetic behavior, which is rare in polyoxovanadate complexes.     

Tetrakis(dimethyltin)-containing tungstophosphate [{Sn(CH3)2}4(H2P4W24O92)2]28-: first evidence for a lacunary Preyssler ion

We demonstrate for the first time that the superlacunary polyanion [H(2)P(4)W(24)O(94)](22)(-) reacts with electrophiles. One-pot reaction of this precursor polyanion with dimethyltin dichloride in aqueous acidic medium results in the hybrid organic-inorganic [{Sn(CH(3))(2)}(4)(H(2)P(4)W(24)O(92))(2)](28)(-) (1). Single-crystal X-ray analysis was carried out on K(17)Li(11)[{Sn(CH(3))(2)}(4)(H(2)P(4)W(24)O(92))(2)].51H(2)O (1a), which crystallizes in the tetragonal system, space group P4(2)/nmc, a = b = 21.5112(17) and c = 27.171(3) A, and Z = 2. Polyanion 1 is composed of two (P(4)W(24)O(92)) fragments that are linked by four equivalent diorganotin groups. The unprecedented assembly 1 has D(2)(d)() symmetry and contains a hydrophobic pocket in the center of the molecule. The cyclic voltammetry pattern of 1 is constituted by a first broad, 16-electron reduction wave followed by a second large current intensity wave. No splitting of the first reduction wave could be obtained at moderate scan rate values, even though two well-separated oxidation processes are associated with it. The characteristics of the first wave are clearly different from those obtained for the polyanion precursor [H(2)P(4)W(24)O(94)](22)(-) and the related, wheel-shaped [H(7)P(8)W(48)O(184)](33)(-), which is due to the {Sn(CH(3))(2)} fragments in 1. However, no feature was observed in the voltammogram which could be associated with reduction of the Sn centers.     

Two three-dimensional {V16Ge4}-based open frameworks stabilized by diverse types of Co(II)-amine bridges and magnetic properties

Two novel three-dimensional (3D) extended vanadogermanate-based frameworks, [Co(pdn)(2)](3)[Co(2)(pdn)(4)][V(16)Ge(4)O(44)(OH)(2)(H(2)O)]·5H(2)O (1), [Co(2)(en)(3)][Co(en)(2)](2)[Co(en)(2)(H(2)O)][V(16)Ge(4)O(44)(OH)(2)(H(2)O)]·10.5H(2)O (2), (pdn = 1,2-propanediamine, en = ethylenediamine) have been synthesized under hydrothermal conditions via changing the organic amine. X-ray crystal structure analyses reveal that both frameworks are built of [V(16)Ge(4)O(44)(OH)(2)(H(2)O)](10-) anions and different Co-amine cations. They represent the first example of incorporating elemental Co into the extended vanadogermanate frameworks. Compound 1 shows a 3D framework with NaCl topology based on {V(16)Ge(4)} clusters as nodes, while compound 2 exhibits a 3D (4,6)-connected network with a Schl?fli symbol of (4(6)·6(7)·8(2))(2)(4(2)·6(4)), which is found for the first time in polyoxovanadate chemistry. The diverse types of metal-organoamine subunits play critical roles in the formation on the final structures. Furthermore, variable temperature susceptibility measurements on compounds 1 and 2 demonstrate the presence of anticipated rare ferrimagnetic behavior.     

NMR studies of heteropolyanion [P(2)W(20)O(70)(H2O)2](-10) complexes with metal cations

We have used multinuclear NMR and IR spectroscopy to study the interaction of a number of metal cations with monovacant heteropolyanion [P(2)W(20)O(7)(0)(H(2)O)(2)](10)(-) (P(2)W(20)) in aqueous solutions starting from its K salt. We have also prepared and studied P(2)W(20) in an Na-only medium. The observed differences in the NMR spectra of NaP(2)W(20)and KP(2)W(20)solutions and the importance of K(+) and Na(+) for the formation of P(2)W(20) suggest that this polyanion exists only as a complex with the alkaline cations. When both cations were simultaneously present in solution, we observed the broadening of the NMR signals of P(2)W(20)due to the Na-K exchange. Li(+) does not replace K(+) or Na(+) in such complexes, and in an Li-only medium P(2)W(20) does not form. Of all the M(n)(+) cations studied (Pd(2+), Bi(3+), Sn(4+), Zr(4+), Ce(4+), Ti(4+), V(5+), and Mo(6+)) only Bi(3+), Sn(4+), and Ce(4+) form complexes with P(2)W(20) in strongly acidic solutions. The (183)W and (119)Sn NMR data suggest that Sn(4+) forms in solution two mutually interconvertable P(2)W(20)Sn complexes of the composition P(2)W(20)O(70)(H(2)O)(3)SnOH(7)(-) and (P(2)W(20)O(70)(H(2)O)(3)Sn)(2)O(14)(-) while Bi(3+) forms one complex of the proposed composition P(2)W(20)O(70)(H(2)O)(2)Bi.(7)(-) We obtained complexes with Bi and Sn as free heteropoly acids and studied their thermostability in the solid state.