Synthesis and Crystal Structure of a Novel Three-dimensional Cu(II) Compound {[Cu(2,2''-bipy)(C7H4O5S)(H2O)2]·(H2O}n

The title compound, {[Cu(2,2'-bipy)(C7H4O5S)(H2O)2](H2O}n (2,2'-bipy = 2,2'- bipyridine), was synthesized by the hydrothermal reaction of Cu(NO3)2(3H2O, 2,2'-bipyridine and 2-sulphobenzoic acid, and structurally characterized by single-crystal X-ray diffraction analysis. The crystal is of triclinic, space group P with a = 9.21(3), b = 10.17(3), c = 10.77(3) (A), α = 77.017(16), β = 89.80(8), γ = 68.46(7)°, V = 911(5) (A)3, Z = 2, (D/s)max = 0.001, Mr = 473.94, Dc = 1.728 g/cm3, μ(MoKα) = 1.365 mm-1, F(000) = 486, the final R = 0.0246 and wR = 0.0628 for 3809 observed reflections with I > 2σ(I). The mononuclear crystal structure extends into a two-dimensional net- work via hydrogen-bonding interactions and a three-dimensional framework is further formed by means of π-π stacking interactions.     

A series of new organic-inorganic molybdenum arsenate complexes based on [(ZnO6)(As3O3)2Mo6O18]4- and [HxAs2Mo6O26](6-x)- clusters as SBUs

By synthesizing the novel molybdenum arsenate complexes, we have obtained eight new structures, namely, (4,4'-bipy)[Zn(4,4'-bipy)2(H2O)2]2[(ZnO6)(AsIII3O3)2Mo6O18].7H2O, 1, [Zn(phen)2(H2O)]2[(ZnO6)(AsIII3O3)2Mo6O18].4H2O, 2, [Zn(2,2'-bipy)2(H2O)]2[(ZnO6)(AsIII3O3)2Mo6O18].4H2O, 3, [Zn(H4,4'-bipy)2(H2O)4][(ZnO6)(AsIII3O3)2Mo6O18].8H2O, 4, (H24,4'-bipy)[CuI(4,4'-bipy)]2[H2AsV2Mo6O26].H2O, 5, (H24,4'-bipy)3[AsV2Mo6O26].4H2O, 6, (H24,4'-bipy)3[AsV2Mo6O26(H2O)].4H2O, 7, and (H24,4'-bipy)2.5(H3O)[AsV2Mo6O26(H2O)].1.25H2O, 8 (4,4'-bipy = 4,4'-bipyridine, 2,2'-bipy = 2,2'-bipyridine, phen = 1,10-phenanthroline). These structures were determined by single-crystal X-ray diffraction analysis and were further characterized by elemental analysis, IR, XPS spectroscopy, and TG analysis. The structure of 1 is constructed from two-dimensional square gridlike sheets linked by the polyanions [(ZnO6)(AsIII3O3)2Mo6O18]4- via hydrogen-bonding interactions to form a three-dimensional supramolecular framework with two types of channels. Compounds 2 and 3 display similar bisupported structures. Compound 4 features a three-dimensional supramolecular architecture. Compound 5 possesses a 1D infinite ladderlike ribbon. Compounds 6-8 are discrete structures exhibiting three isomeric forms of [HxAs2Mo6O26](6-x)-. Furthermore, compound 8 represents a new isomer B'-[As2Mo6O26(H2O)]6-. In addition, the fluorescent properties of compounds 1-3 are reported.     

Discriminating octahedral transition metal ions: highly selective tripodal tris-(2,2'-bipyridine) functionalized piperazine cyclophane receptor for Cu2+ ions

New tripodal transition metal ion receptors, tris(5-ethoxycarbonyl-2,2'-bipyridine) and tris(5-carboxylate-2,2'-bipyridine) substituted 27-membered trimeric piperazine cyclophanes 5 and 7 as well as tetra(5-ethoxycarbonyl-2,2'-bipyridine) substituted 36-membered tetrameric piperazine cyclophane 6, have been prepared and their transition metal ion complexing properties studied in solution by UV-vis spectroscopy and in the solid state by single-crystal X-ray diffraction. The crystal structures of [H(3)5(3+)·Fe(2+)]·4(ClO(4)(-))·CF(3)COO(-) (V), [H(3)7(2+)·Fe(2+)]·2(SO(4)(2-)) (VII) and the reference complex [tris(5,5'-bis(ethoxycarbonyl)-2,2'-bipyridine)Fe(II) perchlorate] (I) showed that the robust piperazine cyclophane is an optimal platform in preorganizing the 2,2'-bipy moieties to form a very fixed octahedral coordination site. In an acidic water solution, the highly preorganized structure of 5 gives a [5·Fe(2+)] complex, the stability of which is comparable with the classical tris(2,2'-bipy) Fe(2+)-complex but it is a significant 3.7 logK units more stable than the non-preorganized tetrameric analog [6·Fe(2+)]. Detailed studies with other similar divalent octahedral transition metal cations showed that the restricted octahedral coordination in complexes of 5 results in an unusual selectivity. The selectivity order [Zn(2+)相似文献   

Hexacyanocobaltate(III) anions as precursors of Co(II)-Ni(II) cyano-bridged multidimensional assemblies: hydrothermal syntheses, crystal and powder X-ray structures, and magnetic properties

Three novel cyanide-bridged heterobimetallic coordination polymers have been synthesized by hydrothermal routes, in superheated water solutions, by using K3[Co(CN)6], NiCl2.6H2O, and alpha-diimine ligands: [Ni(CN)4Co(phen)] (1; phen = 1,10-phenanthroline), [Ni(CN)4Co(2,2'-bipy)] (2; 2,2'-bipy = 2,2'-bipyiridine), and [Ni(CN)4Co(2,2'-bipy)2] (3). The isostructural compounds 1 and 2 contain a two-dimensional network with Co(II) centers octahedrally coordinated by one chelating 2,2'-bipy ligand and four cyanide groups of four distinct [Ni(CN)4]2-, through crystallographically equivalent, bridging units. Compound 3 contains one-dimensional zigzag chains in which the Co(II) ion is coordinated by two chelating 2,2'-bipy ligands and two cyanides from two different [Ni(CN)4]2- units cis to each other. These compounds have been fully characterized by single-crystal or unconventional powder X-ray diffraction analyses and variable-temperature magnetic measurements.     

Formation of a spiral-shaped inorganic-organic hybrid chain, [Cu(II)(2,2'-bipy)(H(2)O)(2)Al(OH)(6)Mo(6)O(18)](n)()(n)()(-): influence of intra- and interchain supramolecular interactions

A novel chainlike coordination polymer [Cu(II)(2,2'-bipy)(H(2)O)(2)Al(OH)(6)Mo(6)O(18)](n)()(n)()(-), formed from a heteropolyanion [Al(OH)(6)Mo(6)O(18)](3)(-) as a building unit and a copper(II) complex fragment, [Cu(II)(2,2'-bipy)(H(2)O)(2)](2+), as a linker, provides the first example of an extended structure based on an Anderson type of polyanion and a transition metal complex with organic ligand. The intra- and interchain O-H.O hydrogen-bonding interactions are seemingly responsible for the spiral shape of this chain. Crystal data: triclinic space group Ponemacr;, a = 11.2253(18) A, b = 14.5194(17) A, c = 15.2672(10) A, alpha = 112.191(8) degrees, beta = 106.693(9) degrees, gamma = 93.916(13) degrees, and Z = 2.     

Mo(W)/Cu/S cluster-based supramolecular arrays assembled from preformed clusters [Et4N]4[WS4Cu4I6] and [(n-Bu)4N]2[MoOS3Cu3X3] (X = I, SCN) with flexible ditopic ligands

In our working toward the rational design and synthesis of cluster-based supramolecular architectures, a set of new [WS4Cu4]- or [MoOS3Cu3]-based supramolecular assemblies have been prepared from reactions of preformed cluster compounds [Et4N]4[WS4Cu4I6] (1) and [(n-Bu)4N]2[MoOS3Cu3X3] (2, X = I; 3, X = SCN) with flexible ditopic ligands such as dipyridylsulfide (dps), dipyridyl disulfide (dpds), and their combinations with dicyanamide (dca) anion and 4,4'-bipy. The cluster precursor 1 reacted with dps or dpds and sodium dicyanamide (dca) in MeCN to produce [WS4Cu4I2(dps)3].2MeCN (4.2MeCN) and [WS4Cu4(dca)2(dpds)2].Et2O.2MeCN (5.Et2O.2MeCN), respectively. On the other hand, treatment of 2 with dpds in DMF/MeCN afforded [MoOS3Cu3I(dpds)2].0.5DMF.2(MeCN)0.5 (6.0.5DMF.2(MeCN)0.5) while reaction of 3 with sodium dicyanamide (dca) and 4,4'-bipy in DMF/MeCN gave rise to [MoOS3Cu3(dca)(4,4'-bipy)1.5].DMF.MeCN (7.DMF.MeCN). Compounds 4.2MeCN, 5.Et2O.2MeCN, 6.0.5DMF.2(MeCN)0.5, and 7.DMF.MeCN have been characterized by elemental analysis, IR spectroscopy, and single-crystal X-ray crystallography. Compound 4 contains a 2D layer array made of the saddle-shaped [WS4Cu4] cores interlinked by three pairs of Cu-dps-Cu bridges. Compound 5 has another 2D layer structure in which the [WS4Cu4] cores are held together by four pairs of Cu-dca-Cu and Cu-dpds-Cu bridges. Compound 6 displays a 1D spiral chain structure built of the nido-like [MoOS3Cu3] cores via two pairs of Cu-dpds-Cu bridges. Compound 7 consists of a 2D staircase network in which each [MoOS3Cu3(4,4'-bipy]2 dimeric unit interconnects with four other equivalent units by a pair of 4,4'-bipy ligands and two pairs of dca anions. The [WS4Cu4] core in 4 or 5 and the [MoS3Cu3] core in 7 show a planar 4-connecting node and a seesaw-shaped 4-connecting node, respectively, which are unprecedented in cluster-based supramolecular compounds. The successful assembly of 4-7 from the three cluster precursors 1-3 through flexible ditopic ligands provides new routes to the rational design and construction of complicated cluster-based supramolecular arrays.     

二苯乙醇酸铜配合物的合成、晶体结构、电化学和荧光性质

以二苯乙醇酸为配体合成了1个新的化合物[Cu(2,2′-bipy)(BAA)][Cu(2,2′-bipy)(BAA)(H2O)]2.(H2O)3(BAA=二苯乙醇酸阴离子,2,2′-bipy=2,2′-联吡啶)。该化合物晶体属三斜晶系,空间群P1,晶胞参数:a=1.121 7(5)nm,b=1.360 2(6)nm,c=2.335 2(10)nm,α=99.260(6)°,β=101.223(8)°,γ=94.805(8)°,V=3.425(3)nm3,Dc=1.385 g.cm-3,Z=6,μ(Mo Kα)=0.992 mm-1,F(000)=1 474,最终偏离因子R1=0.0561,wR2=0.1128。在标题化合物的不对称单元中有3个单核铜(Ⅱ)配合物,且3个中心铜(Ⅱ)离子的配位数不完全相同,如Cu(1)离子的配位数是4,而Cu(2)和Cu(3)离子的配位数都是5。本文还测定了标题化合物的电化学性能和荧光性能,结果表明:在电化学过程中配合物的电子转移是准可逆的,电子转移数为2个;配合物在478 nm的光激发下可发射荧光。     

一维螺旋链状配位聚合物[Cu(p-BDOA)(2，2′-bipy)·H2O]n的合成与表征(英)

A new copper(Ⅱ) coordination polymer, [Cu(p-BDOA)(2，2′-bipy)·H₂O]_n ( p-BDOA^2-=benzene-1,4-dioxyacetate dianion; 2,2′-bipy=2,2′-bipyridine) has been synthesized and characterized by elemental analysis, IR, TG and single crystal X-ray diffraction. The Crystal crystallizes in orthorhombic system, the space group is P2₁2₁2₁, with the unit cell parameters a=0.698 4(1) nm, b=1.559 7(3) nm, c=1.750 6(4) nm and V=1.906 8(7) nm³, M_r=461.91, Z=4, R=0.057 5, wR=0.078 3. Each copper(Ⅱ) atom is six-coordinated and displays a distorted square pyramidal geometry with a one-capped base by one very long semicoordinate Cu-O(carboxylate) bond. Adjacent Cu(Ⅱ) ions are bridged by carboxylate groups, resulting in a one-dimensional helical chain. The adjacent Cu…Cu distance within the polymeric chain is 1.348 4 nm. Furthermore, such chains are linked through hydrogen bonds and π-π stacking interactions to form supramolecular network. CCDC: 219234.     

刚性配体2,2-联吡啶诱导的双咪唑金属超分子配合物的合成与晶体结构

合成了3种新的超分子配合物[Cd(H2biim)(2,2'-bipy)(NO3)2] (1), [Cu(H2biim)(2,2'-bipy)(H2O)](NO3)2 (2)和[Zn(H2biim)(2,2'-bipy)(H2O)](NO3)2 (3) (H2biim＝双咪唑; 2,2'-bipy＝2,2'-联吡啶), 并通过X射线单晶衍射测定了其结构. 配合物1～3均为单斜晶系, 属于P2(1)/c空间群, 在1中, Cd(II)为六配位, 它与双咪唑的2个氮原子, 联吡啶的2个氮原子和2个硝酸根的2个氧原子配位. 在2和3中, Cu(II)和Zn(II)均为五配位的, 它们与双咪唑的2个氮原子、2,2'-联吡啶的两个氮原子和一个水分子配位. 1～3的对称单元均通过双咪唑、硝酸根和水之间形成的氢键R21(7), R21(4) 和R44(18)构筑了1D链状超分子.     

Two series of novel rare earth complexes with dicyanamide [Ln(dca)2(phen)2(H2O)3][dca].(phen), (Ln = Pr, Gd, and Sm) and [Ln(dca)3(2,2'-bipy)2(H2O)]n, (Ln = Gd, Sm, and La): syntheses, crystal structures, and magnetic properties

Two series of novel complexes, [Ln(dca)(2)(Phen)(2)(H(2)O)(3)](dca).(phen) (Ln = Pr (1), Gd (2), and Sm (3), dca = N(CN)(-), phen = 1,10-phenanthroline) and [Ln(dca)(3)(2,2'-bipy)(2)(H(2)O)](n), (Ln = Gd (4), Sm (5), and La (6), 2,2'-bipy = 2,2'-bipydine), have been synthesized and structurally characterized by X-ray crystallography. The crystal structures of the first series (1-3) are isomorphous and consist of discrete [Ln(dca)(2)(Phen)(2)(H(2)O)(3)]+ cations, dca anions, and lattice phen molecules; whereas the structures of the second series (4-6) are characterized by infinite chains [Ln(dca)(3)(2,2'-bipy)(2)(H(2)O)](n). The Ln(III) atoms in all complexes are nine-coordinated and form a distorted tricapped trigonal prism environment. The three-dimensional frameworks of 1-6 are constructed by intermolecular hydrogen bond interactions. Variable-temperature magnetic susceptibility measurements for complexes 1, 2, 4, and 5 indicate a Curie-Weiss paramagnetic behavior over 5-300 K.     

Hydrothermal syntheses, crystal structures, and magnetic properties of inorganic-organic hybrid vanadium selenites with zero- to three-dimensional structures: (1,10-phenanthroline)(2)V(2)SeO(7), (2,2'-bipyridine)VSeO(4), (4,4'-bipyridine)V(2)Se(2)O(8), and (4,4'-bipyridine)(2)V(4)Se(3)O(15).H(2)O

A family of inorganic-organic hybrid vanadium selenites with zero-, one-, two-, and three-dimensional structures, (1,10-phen)(2)V(2)SeO(7), (2,2'-bipy)VSeO(4), (4,4'-bipy)V(2)Se(2)O(8), and (4,4'-bipy)(2)V(4)Se(3)O(15).H(2)O (where phen = phenanthroline and bipy = bipyridine), were hydrothermally synthesized and characterized by single-crystal X-ray diffraction. Different bidentate organodiamine ligands and reactant concentrations were used in the four reaction systems, which are responsible for the variety of structural dimensions of the compounds. (1,10-phen)(2)V(2)SeO(7) crystallizes in a monoclinic system with space group P2(1)/n and cell parameters a = 8.6509(3) A,( )b = 7.8379(2) A, c = 34.0998(13) A, beta = 91.503(2) degrees, and Z = 4. (2,2'-bipy)VSeO(4) crystallizes in a monoclinic system with space group C2/c and cell parameters a = 17.0895(12) A, b = 14.7707(10) A, c = 11.7657(8) A, beta = 131.354(3) degrees, and Z = 8. (4,4'-bipy)V(2)Se(2)O(8) crystallizes in a triclinic system with space group Ponemacr; and cell parameters a = 7.1810(10) A, b = 10.8937(13) A, c = 11.1811(15) A, alpha = 115.455(3) degrees, beta = 107.582(3) degrees, gamma = 91.957(4) degrees, and Z = 2. (4,4'-bipy)(2)V(4)Se(3)O(15).H(2)O crystallizes in a monoclinic system with space group Pc and cell parameters a = 7.9889(9) A, b = 7.8448 A, c = 23.048(3) A, beta = 99.389(4) degrees, and Z = 2. (1,10-phen)(2)V(2)SeO(7) has an isolated structure, (2,2'-bipy)VSeO(4) has a chain structure, (4,4'-bipy)V(2)Se(2)O(8) has a layered structure, and (4,4'-bipy)(2)V(4)Se(3)O(15).H(2)O has a framework structure. The chains are constructed from VO(4)N(2) octahedra and SeO(3) pyramids, laced by organic ligands (2,2'-bipy). The layers consist of vanadium selenite chains [(VO)(2)(SeO(3))(2)]( infinity ), linked by 4,4'-bipy molecules. The framework is composed of vanadium selenite sheets [V(4)Se(3)O(16)]( infinity ), pillared by 4,4'-bipy molecules. All of the compounds are thermally stable to 300 degrees C, and the magnetic susceptibilities confirm the existence of tetravalent V atoms in the antiferromagnetic (4,4'-bipy)V(2)Se(2)O(8) complex and mixed tetravalent and pentavalent V atoms in the paramagnetic complex (4,4'-bipy)(2)V(4)Se(3)O(15).H(2)O.     

Synthesis, Crystal Structure and Electrochemical Properties of Complex[Ni(2,2''-bipy)2(ClC6H4COO)(H2O)](ClO4)

A new nickel(Ⅱ) coordination complex [Ni(2,2'-bipy)2(ClC6H4COO)(H2O)](ClO4) was synthesized by self-assembly reaction of m-chlorobenzoic acid, 2,2'-bipy and Ni(ClO4)2(6H2O. The crystal of the title compound belongs to monoclinic system, space group P21/n with a = 0.77764(14), b = 2.6572(5), c = 1.3637(2) nm, β = 96.456(3)°, V = 2.8000(9) nm3, Dc = 1.528 g/cm3, Z = 4, Mr = 644.10, μ(MoKα) = 0.937 mm-1, F(000) =1320, R = 0.0549 and wR = 0.1164. Structure analysis shows that the nickel(Ⅱ) ion is coordinated with four nitrogen atoms from two bipys as well as two oxygen atoms from m-chlorobenzoic acid and water, respectively, giving a distorted octahedral coordination geometry. The cyclic voltametric behavior of the complex is also presented.     

Unsymmetrical surface modification of a heteropolyoxotungstate via in-situ generation of monomeric and dimeric copper(II) species

Unsymmetrical functionalization of a discrete alpha-{SiW12O40} Keggin with two heterometallic building blocks, a Cu(II) dimer and a Cu(II) monomer, results in the formation of [{Cu2(O2CMe)2(5,5'-dimethyl-2,2'-bipy)2}{Cu(5,5'-dimethyl-2,2'-bipy)2}SiW12O40] that displays interesting physical properties.     

Syntheses, structures, and characterizations of four new lead(II) 5-sulfosalicylate complexes with both chelating and bridging neutral ligands

Four structurally diverse complexes, {[Pb(Hssal)(2,2'-bipy)](4,4'-bipy)0.5}n (1), [Pb2(Hssal)2(2,2'-bipy)2(4,4'-bipy)(H2O)2] (2), [Pb(Hssal)(phen)(4,4'-bipy)0.5]n (3), and [Pb(Hssal)(2,2'-bipy)(bpe)0.5]n (4), have been synthesized and characterized by elemental analyses, IR, thermogravimetric analyses, fluorescent spectra, and single-crystal X-ray analyses, where Hssal2- is doubly deprotonated 5-sulfosalicylate, 2,2'-bipy is 2,2'-bipyridine, phen is 1,10-phenanthroline, 4,4'-bipy is 4,4'-bipyridine, and bpe is trans-1,2-bis(4-pyridyl)ethylene. The structure of complex 1 possesses a one-dimensional ladderlike chain with guest 4,4'-bipy molecules, while the molecular structure of complex 2 is a dimeric species with a coordinating 4,4'-bipy ligand. Complex 3 consists of a one-dimensional ladderlike chain with monodentate 4,4'-bipyridine but somewhat different from that of complex 1. Complex 4 is a two-dimensional layer structure. In 1-4, all 5-sulfosalicylates are doubly deprotonated, and all carboxylate groups of Hssal2- chelate to PbII ions; however, the coordination modes of sulfonyl groups are different: syn-syn bridging in 1, noncoordinating in 2, syn-skew bridging in 3, and one-atom bridging in 4. The noncoordinating mode of sulfonate in PbII complexes containing 5-sulfosalicylate is first reported in this presentation. The 4,4'-bipy ligands act as guest molecules in 1, dimeric linkers in 2, and monodentates in 3. The pi-pi stacking interactions can be observed in complexes 1-3, whereas there is no such interaction in complex 4. The coordination spheres of PbII ions in 1-4 are controlled by three factors: the activity of a lone pair of electrons, weak Pb-O interactions, and pi-pi stacking interactions. The PbII lone pair in 4 is inactive, whereas in 1-3, they are stereochemically active. The thermal stability and fluorescent property of complexes 1-4 are different from those of PbII complexes only containing chelating ligands, [Pb(Hssal)(2,2'-bipy)(DMF)]n (5), and [Pb(Hssal)(2,2'-bipy)(H2O)]n (6), and [Pb(Hssal)(phen)(DMF)]n (7).     

Hydrothermal Synthesis, Crystal Structure and Fluorescent Property of a Keggin Polyoxometalate [CuI(2,2''-bipy)2]3[PWⅥ12O40]

A Keggin-type tungstohosphate compound [CuI(2,2'-bipy)2]3[PWVI12O40] 1 (bipy = bipyridine) was prepared by the hydrothermal method for the first time. Single-crystal X-ray diffraction revealed that 1 (C60H48Cu3N12O40PW12) crystallizes in the monoclinic system, space group P21/c with a = 16.9837(10), b = 17.9732(13) c = 27.8701(13)(A), β = 96.1039(10)°, V = 8459.2(9)(A)3, Mr = 4004.89, Z = 4, Dc = 3.145 g/cm3, μ = 17.089 mm-1, F(000) = 7208, S = 1.005, the final R = 0.0469 and wR = 0.0827 for 10807 observed reflections (I > 2σ(I)). Compound 1 consists of one discrete normal Keggin polyanion [PWVI12O40]3- and three isolated coordinated cat- ions [CuI(2,2'-bipy)2]+. Significantly, there exist three crystallographically independent asymmetric reduced copper (I) centers in 1. Furthermore, the compound shows strong photoluminescence property in solid state at room temperature.     

Influence of the reaction conditions on the self-assembly of lead(II) 5-sulfosalicylate coordination polymers with chelating amine ligands

The synthesis and crystal structures of [Pb(Hssal)(2,2'-bipy)(DMF)]n (1), [Pb(Hssal)(2,2'-bipy)(H2O)]n (2), [Pb(Hssal)(phen)(DMF)]n (3), and [Pb3(ssal)2(phen)3]n (4) were reported, where Hssal2- and ssal3- are doubly and fully deprotonated 5-sulfosalicylates, 2,2'-bipy is 2,2'-bipyridine, and phen is 1,10-phenanthroline. Compounds 1-4 were synthesized by the various reaction conditions, such as reaction temperature, molar ratio, and pH, and these structures are formed by infinite chains or layers where Pb(II) ions are linked by Hssal2- or ssal3- bridges. Compound 1, which has a ladderlike chain, was formed in DMF/H2O. Compound 2 with a H2O molecule coordinated to Pb(II) was prepared by a hydrothermal reaction. Compounds 3 and 4 were synthesized in a higher pH compared to compounds 1 and 2, containing the 2,2'-bipy ligand. In 1-3, 5-sulfosalicylates are doubly deprotonated, whereas in 4, 5-sulfosalicylate is fully deprotonated. Coordination modes of Hssal2- and ssal3- ligands in 1-4 are novel and are first reported in this presentation. Although compounds 1 and 3 have the same structural topology, their aromatic-aromatic interactions are significantly different. The coordination spheres of Pb(II) ions in 1 and 3 are holodirected, whereas in 2 and 4, they feature somewhat hemidirected properties with small holes or gaps. Compound 4 exhibits some interesting features that (1) there is not any solvent in the structure, (2) there are extensively aromatic-aromatic stacking interactions among aromatic rings, and (3) there is also a weak interaction between Pb(II) atoms in the trinuclear motif.     

A new extended structural compound based on saturated Wells-Dawson polyoxoanions

A new 3D extended structural compound,(dpdo)_2H_2{[Cu(2,2'-bipy)_2]_2(P_2W_(18)O_(62))}·5H_2O 1(dpdo = 4,4'-bipyridine-N,N'-dioxide; 2,2'-bipy = 2,2'-bipyridine),has been hydrothermally synthesized and characterized by elemental analyses,IR,TG analyses,cyclic voltammetry,and single-crystal X-ray diffraction.Compound 1 is built up of[P_2W_(18)O_(62)]~(6-) cluster as the structural motif covalently linked by[Cu(2,2'-bipy)_2]~(2+) coordination complexes to yield the 1D chains,which are further in close cont...     

Hydrothermal Synthesis and Crystal Structure of a Hybrid Compound Based on β-Octamolybdate [Mn(2,2’-bipy)_3]_2[β-Mo_8O_(26)]·4H_2O

1 INTRODUCTION Polyoxometalates (POMs) are one of the most widely used inorganic components due to their at- tractive electronic and molecular properties with va- rious applications in catalysis, medicine, materials science[1～3] and so on. Exploration of transition me- tal complex cations as well as organic component which functions as ligand as building blocks in the construction of metal oxide composite materials is a fruitful strategy[4, 5]. Among the polyoxometalates studied to dat…     

ESI-MS and thermal melting studies of nanoscale platinum(II) metallomacrocycles with DNA

The hydrophilic, long-chain diamine PEGda (O,O'-bis(2-aminoethyl)octadeca(ethylene glycol)), when complexed with cis-protected Pt(II) ions afforded water-soluble complexes of the type [Pt(N,N)(PEGda)](NO(3))(2) (N,N = N,N,N',N'-tetramethyl-1,2-diaminoethane (tmeda), 1,2-diaminoethane (en), and 2,2'-bipyridine (2,2'-bipy)) featuring unusual 62-membered chelate rings. Equimolar mixtures containing either the 16-mer duplex DNA D2 or the single-stranded D2a and [Pt(N,N)(PEGda)](2+) were analyzed by negative-ion ESI-MS. Analysis of D2-Pt(II) mixtures showed the formation of 1 : 1 adducts of [Pt(en)(PEGda)](2+), [Pt(tmeda)(PEGda)](2+) and the previously-described metallomacrocycle [Pt(2)(2,2'-bipy)(2){4,4'-bipy(CH(2))(4)4,4'-bipy}(2)](8+) with D2; the dinuclear species bound to D2 most strongly, consistent with its greater charge and aromatic surface area. D2 formed 1 : 2 complexes with the acyclic species [Pt(2,2'-bipy)(Mebipy)(2)](4+) and [Pt(2,2'-bipy)(NH(3))(2)](2+). Analyses of D2a-Pt(II) mixtures gave results similar to those obtained with D2, although fragmentation was more pronounced, indicating that the nucleobases in D2a play more significant roles in mediating the decomposition of complexes than those in D2, in which they are paired in a complementary manner. Investigations were also conducted into the effects of selected platinum(II) complexes on the thermal denaturation of calf thymus DNA (CT-DNA) in buffered solution. Both [Pt(2)(2,2'-bipy)(2){4,4'-bipy(CH(2))(6)4,4'-bipy}(2)](8+) and [Pt(2,2'-bipy)(Mebipy)(2)](4+) stabilized CT-DNA. In contrast, [Pt(tmeda)(PEGda)](2+) and [Pt(en)(PEGda)](2+) (as well as free PEGda) caused negligible changes in melting temperature (ΔT(m)), suggesting that these species interact weakly with CT-DNA.     

Crystal Structure of catena-[(Tetrakis-μ2-acetato-μ2-4,4'-bipyridine) dicopper(Ⅱ)] Acetonitrile Solvate

The title compound,[Cu2(CH3COO)4(C8H10N2)]n·nCH3CN1 (C8H10N2,4,4'-bipy = 4,4'-bipyridine),has been solvothermally synthesized in CH3CN and characterized by X-ray diffraction.The crystal is of monoclinic,space group Cc with a = 22.626(6),b = 14.012(4),c =15.106(4) (A),β = 107.610(3)°,V = 4565(2) (A)3,C20H23Cu2N3O8,Mr = 560.49,Z = 8,Dc = 1.631 g/cm3,μ = 1.914 mm-1,Flack parameter = 0.48(1),F(000) = 2288,R = 0.042 and wR = 0.)98 for 8887 observed reflections (I ＞ 2σ(I)).It consists of nearly linear one-dimensional chains [Cu2(CH3COO)4(C8H10N2)]n derived from paddle-wheel [Cu2(CH3COO)4] unit linked by 4,4'-bipy,and CH3CN as guest molecule regularly decorates between the chains.