Synthesis and Crystal Structur of (4,4′-H_2bipy)[CdBr_4]·H_2O

The title compound (4,4′-H2bipy)[CdBr4]·H2O 1 has been synthesized via hydrothermal reaction and characterized by X-ray diffraction. The crystal belongs to monoclinic,space group P21/c with a=8.260(3),b=23.926(7),c=9.774(2),β=106.777(9)o,C10H12Br4CdN2O,Mr=608.26,V=1849.4(9)3,Z=4,Dc=2.185 g/cm3,S=1.005,μ(MoKα) =9.814 mm–1,F(000)=1128,R=0.0646 and wR=0.0989. The crystal structure analysis of 1 reveals that the title compound features an isolated structure,based on discrete 4,4′-H2bipy moieties and lattice water molecules which are linked by hydrogen bonds together with tetra-hedral cadmium atoms terminally coordinated by four bromine atoms.     

Syntheses and(Crystal Structures of Two New One-dimensional Double Hydrogen-bonding-chain Complexes [Ni(bipy)2Cl]·ClO4 and [Zn(bipy)2Cl]·BF4

Two new transition metal complexes, [Ni(bipy)2Cl]·ClO4 (bipy = 2,2'-bipyridine) 1 and [Zn(bipy)2Cl]·BF4 2, have been synthesized and characterized by single-crystal X-ray diffraction analysis. Both 1 and 2 crystallize in monoclinic space group P21/n with Z = 4. For 1, a = 10.776(1), b = 12.067(1), c = 16.146(2)(A), β= 93.021(2)o, V = 2031.9(4)(A)3, Mr = 505.98, Dc = 1.654 g/cm3, μ = 1.255 mm-1, F(000) = 1032, the final R = 0.0406 and wR = 0.1002 for 3983 observed reflections with Ⅰ ＞ 2σ(I). For 2, a = 10.758(4), b = 12.058(4), c = 16.135(5) (A), β = 104.57(1)o, V = 2025.7(12) (A)3, Mr = 500.00, Dc = 1.639 g/cm3, μ = 1.396 mm-1, F(000) = 1008, the final R = 0.0470 and wR = 0.1237 for 3759 observed reflections with Ⅰ ＞ 2σ(I). The crystal structures of 1 and 2 are isostructural with very similar supramolecular structures. A one-dimen- sional zigzag double hydrogen-bonding-chain is generated by the intermolecular M-bipy …anion…bipy--M hydrogen bonding interactions between the chelating ligands of bipy and anion.     

A Novel Layered Complex with Rhomboidal Channels:Hydrothermal Synthesis, Crystal Structure, and Properties of Cu(4,4′-bipy)2(H2PO4)2(H2O)2 (bipy=bipyridine)

The combination of both 4,4′-bipyridine(4,4′-bipy) and dihydrogen phosphate anion ligands with copper(Ⅱ) results in the formation of a novel layered compound Cu(4,4′-bipy)2(H2PO4)2(H2O)2. The crystal structure comprises discrete neutral Cu(4,4′-bipy)2(H2PO4)2(H2O)2 units. The copper atom, located on the crystallographic twofold axis, is coordinated with two nitrogen atoms of terminal 4,4′-bipy ligands and two water molecules at the equatorial positions, and two dihydrogen phosphate oxygen atoms at the axial positions, forming an elongated octahedron. The complex is a two-dimensional distorted rhomboidal network possessing two kinds of rhomboids with dimensions of ca. 1.6792 nm×0.3203 nm and 1.2778 nm×0.3198 nm, respectively. The two-dimensional networks are stacked parallelly on each other along c-axis to give an extended three-dimensional channel network with an interlayer distance of ca. 0.5030 nm. Crystal data: triclinic, space group P-1, a=1.0253(2) nm, b=1.4501(3) nm, c=0.79715(16) nm, α=97.91(3)°, β=90.99(3)°, γ=85.54(3)°, V=1.1703(4) nm3, Z=2, R=0.0892, wR=0.2451.     

A Novel Layered Complex with Rhomboidal Channels:Hydrothermal Synthesis,Crystal Structure,and Properties of Cu(4,4''''-bipy)_2(H_2PO_4)_2(H_2O)_2 (bipy=bipyridine)

IntroductionMetalcoordinationpolymerswithvariablechan nelsorcavitiesarecurrentlyofinterestduetotheirpotentialfunctionsasmicroporoussolidmaterialsformolecularadsorption ,ionexchange ,molecularmag nets,andshape selectivecatalysis[1— 3] .Amajorre searchefforthasbeenfocusedonusingthemolecularbuildingblockapproachtogeneratesuchmicroporousmaterials[3— 5] .Beinganalogoustopyrazine ,therigidrod like 4 ,4′ bipyridine(4 ,4′ bipy)ligandisausefulbuildingblockfortheconstructionofmetal organicco ordinat…     

Synthesis,Crystal Structures and Magnetic Properties of Two Methoxo-Bridged Dimeric Copper(II) Complexes [Cu 2(APMD)4(μ2-OMe) 2 ]X 2(APMD = 2-aminopyrimidine; X = BF4 or CIO4)

Two bis-methoxo-bridged dimeric copper(II) complexes, [Cu₂(OMe)₂(APMD)₄](BF₄)₂ 1 and [Cu₂(OMe)₂(APMD)₄](ClO₄)₂ 2, were prepared and characterized by x-ray single-crystal structure analysis and magnetic susceptibility. Complexes 1 and 2 are isomorphous, being composed of discrete [Cu₂( w 2-OMe)₂(APMD)₄]²⁺ cations and anions with each Cu(II) atom ligated by two pyrimidine nitrogen atoms (Cu-N , 2.01Å) from two APMD ligands and two oxygen atoms (Cu-O , 1.92Å) from the w 2 -methoxo groups in a distorted square-planar geometry. The intramolecular metal-metal separations in the two complexes are ca. 2.95 Å. The intermediate antiferromagnetic exchanges (J , m 270 cm^-1) for the two complexes indicate a good overlap between the electronic orbitals of the square-planar copper(II) center via bridging oxygen atoms.     

Synthesis and Crystal Structur of （4,4＇-H2bipy）[CdBr4]-H2O

The title compound (4,4'-H2bipy)[CdBr4]·H2O 1 has been synthesized via hydrothermal reaction and characterized by X-ray diffraction. The crystal belongs to monoelinic,space group P21/c with a=8.260(3), b=23.926(7), c=9.774(2) (A), β=106.777(9)°,C10H12Br4CdN2O, Mr=608.26, V=1849.4(9)(A)3, Z=4, Dc=2.185 g/cm3, S=1.005, μ(MoKα)=9.814 mm-1, F(000)=1128, R=0.0646 and wR=0.0989. The crystal structure analysis of 1reveals that the title compound features an isolated structure, based on discrete 4,4'-H2bipy moieties and lattice water molecules which are linked by hydrogen bonds together with tetrahedral cadmium atoms terminally coordinated by four bromine atoms.     

层状金属配位聚合物[{NiX2（bipy）}n]（X=F,Cl,Br,I;bipy=4,4‘—bipy …

用紧束缚晶体轨道方法对层状金属配位聚合物「｛ＮｉＸ２（ｂｉｐｙ）｝ｎ「（Ｘ＝Ｆ，Ｃｌ，Ｂｒ，Ｉ；ｂｉｐｙ＝４，４’－ｂｉｐｙｒｉｄｙｌ）进行了能带结构计算，并利用键向量方法对这一系列聚合物能带特征和成键性质进行了讨论。     

Hydrothermal Synthesis,Crystal Structures and Magnetic Properties of two Bimetallic Cage Cluster Vanadate Complexes [Co(phen)2]2V4O12 and [Co(2,2′-bipy)2]2V4O12

Two new bimetallic cluster complexes, [Co(phen)₂]₂V₄O₁₂ 1 (phen = phenanthroline) and [Co(2,2'-bipy)₂]₂V₄O₁₂ 2 (2,2'-bipy = 2,2'-bipyridine), have been synthesized hydrothermally. X-ray crystallography reveals that both 1 and 2 possess a similar metal cage cluster core, Co₂V₄O₁₂. Magnetic studies of 1 and 2 indicate that both the complexes exhibit antiferromagnetic interactions between the cobalt(II) ions.     

Synthesis,Crystal Structure,and Properties of [Dy(p-ABA)3Phen · H2O] · 1.5H2O1

(1.10-Phenanthroline)-tris(4-amidobenzoate)dysprosium, [Dy(p-ABA)₃Phen · H₂O] · 1.5H₂O (where p-ABA = p-amidobenzoate and Phen = 1.10-phenanthroline) has been synthesized. The complex was characterized by elemental analysis, UV, IR spectroscopy, and molar conductance. The crystal structure was determined by X-ray crystallography. The coordination number of the mononuclear complex is nine. The crystals are triclinic, space group P1 with a = 10.4484(13) Å, b = 12.2015(15) Å, c = 14.0170(17) Å; α = 92.800(2)°, β = 102.7220(10)°, γ = 108.880(2)°. Z = 2, d _c = 1.617 mg m^?3, F(000) = 786. R1 = 0.0327, and wR2 = 0.0911.     

Syntheses and Crystal Structures of Two New One-dimensional Double Hydrogen-bonding-chain Complexes [Ni(bipy)_2Cl]·ClO_4 and [Zn(bipy)_2Cl]·BF_4

Two new transition metal complexes, [Ni(bipy)2Cl]·ClO4 (bipy = 2,2'-bipyridine) 1 and [Zn(bipy)2Cl]·BF4 2, have been synthesized and characterized by single-crystal X-ray diffraction analysis. Both 1 and 2 crystallize in monoclinic space group P21/n with Z = 4. For 1, a = 10.776(1), b = 12.067(1), c = 16.146(2) , β = 93.021(2)o, V = 2031.9(4) 3, Mr = 505.98, Dc = 1.654 g/cm3, μ = 1.255 mm–1, F(000) = 1032, the final R = 0.0406 and wR = 0.1002 for 3983 observed reflections with I > 2σ(I). For 2, a = 10.758(4), b = 12.058(4), c = 16.135(5) , β = 104.57(1)o, V = 2025.7(12) 3, Mr = 500.00, Dc = 1.639 g/cm3, μ = 1.396 mm–1, F(000) = 1008, the final R = 0.0470 and wR = 0.1237 for 3759 observed reflections with I > 2σ(I). The crystal structures of 1 and 2 are isostructural with very similar supramolecular structures. A one-dimen-sional zigzag double hydrogen-bonding-chain is generated by the intermolecular M-bipy ···anion···bipy- M hydrogen bonding interactions between the chelating ligands of bipy and anion.     

Synthesis, Properties and Crystal Structure of a New Bismuth Oxalate:Na(C5NH6)[Bi(H2O)(C2O4)2]2·4H2O

A new bismuth oxalate Na(C5NH6)[Bi(H2O)(C2O4)2]2.4H2O has been obtained under hydrothermal conditions and characterized by X-ray diffraction.It crystallizes in mono-clinic, space group C2/m with a = 12.020(5), b = 11.190(8), c = 11.067(10)(A), β= 121.78(2)°,NaBi2CI3NH18O22, Mr= 981.24, V = 1265.4(16)(A)3, Z = 2, Dc = 2.575 g/cm3, μ(MoKα) = 14.005 mm-1, F(000) = 912, R = 0.0179 and wR = 0.0394.In the structure, the Bi(Ⅲ) centers are interconnected by oxalate ligands to produce honeycomb-like layers, which are further pillared by bridging ligand oxalate molecules to form a 3-D open-framework structure.Furthermore, the title compound exhibits blue luminescence with the emission peaks located at 394nm in the solid state at room temperature, and thus it could be useful in the field of photoactive materials.     

Synthesis and Crystal Structure of Bridging Complex [Cu_2(bipy)_2·OAc·Cl·OH]·TsTausH·3H_2O

1 INTRODUCTION The binuclear complexes have been widely studied in many fields, such as catalysis, semi- conductor and bioinorganic chemistry because of their rich physical and chemical properties[1～4]. The complexes with N-P-tolysulonyl--amino acids ha…     

Synthesis,Crystal and Molecular Structures of [Co(MH)2(Thio)2][BF4] · H2O and [Co(DH)2(NH3)2][BF4]

Crystal structures of [Co(MH)₂(Thio)₂][BF₄] · H₂O (I) and [Co(DH)₂(NH₃)₂][BF₄] (II), where MH^– is H₃C–C(NOH)–C(NO^–)–H and DH^– is H₃C–C(NOH)–C(NO^–)–CH₃, were determined by X-ray diffraction. The crystals are monoclinic, space group C2/c, unit cell parameters (for I and II, respectively): a = 22.018(2) Å, b = 7.943(1) Å, c = 11.681(1) Å, = 92.68(1)° and a = 21.436(2) Å, b = 6.400(2) Å, c = 12.389(2) Å, = 113.13(1)°. In both cases, the Co(III) coordination polyhedron is a centrosymmetrical trans-octahedron, N₄S₂ for I and N₆ for II. In the crystals of I and II, the complex cations and the outer-sphere [BF₄]^– anions (and the crystal water molecules in I) form elaborate hydrogen bonding system.     

Photoelectron Spectroscopy and Structures of X−⋅⋅⋅CH2O (X=F,Cl, Br,I) Complexes

A combined experimental and theoretical approach has been used to investigate X⁻⋅⋅⋅CH₂O (X=F, Cl, Br, I) complexes in the gas phase. Photoelectron spectroscopy, in tandem with time-of-flight mass spectrometry, has been used to determine electron binding energies for the Cl⁻⋅⋅⋅CH₂O, Br⁻⋅⋅⋅CH₂O, and I⁻⋅⋅⋅CH₂O species. Additionally, high-level CCSD(T) calculations found a C_2v minimum for these three anion complexes, with predicted electron detachment energies in excellent agreement with the experimental photoelectron spectra. F⁻⋅⋅⋅CH₂O was also studied theoretically, with a C_s hydrogen-bonded complex found to be the global minimum. Calculations extended to neutral X⋅⋅⋅CH₂O complexes, with the results of potential interest to atmospheric CH₂O chemistry.     

Synthesis,Crystal Structure and Luminescence Property of [MnL2（bipy）（H2O）2]n

A new one-dimensional Mn（Ⅱ） complex, [MnL2（bipy）（H2O）2]n 1, has been obtained by the reaction of MnCl2·4H2O, 2,2＇-bipyridine （bipy） and 1-（4-phenoxyacetate）-5-thioacetatetetrazole （H2L）. The crystal crystallizes in the triclinic system, space group Pi with a = 7.6088（2）, b = 12.2795（2）, c = 13.6617（3）A, α = 75.416（2）, β =79.264（2）, γ = 74.271（2）°, V = 1179.48（4） A3, Z = 2, Mr = 555.43, F（000） = 570, Dc = 1.564 g/cm^3, μ = 0.704 mm^-1, the final R = 0.0454 and wR = 0.0849 for 3127 observed reflections （Ⅰ〉 2σ（Ⅰ））. The Mn（Ⅱ） is six-coordinated by two water molecules, two N atoms from bipy and two carboxylate O atoms from two L^2- to form a distorted octahedral geometry. Each L^2- ligand serves as a bridging ligand to link two Mn（Ⅱ） atoms, leading to a single-strand zigzag coordination polymer. Hydrogen-bonding interactions between adjacent chains as well as π-π stacking interactions extend the complex into a three-dimensional supramolecular architecture. Moreover, the title compound emits strong red fluorescent light （λem（max） = 610 nm） in EtOH solution.     

In situ synthesis and structure of FeCl4(4,4′-diethyl-4,4′-bipyh) (bipy = bipyridine)

A novel viologen(4,4′-bipyridinium)-based compound FeCl₄(4,4′-diethyl-4,4′-bipyH) (1) (bipy = bipyridine), in which 4,4′-diethyl-4,4′-bipyH (MQ ⁺) was generated in situ, is synthesized via the hydrothermal reaction and structurally characterized by single crystal X-ray diffraction. The crystal structure analysis reveals that the title compound features an isolated structure based on 4,4′-diethyl-4,4′-bipyH moieties and an iron atom terminally bound by four chlorine atoms. The 4,4′-diethyl-4,4′-bipyH moieties and (FeCl₄)^? anions are interconnected by hydrogen bonds to form a 3D supramolecular framework.     

Synthesis, Crystal Structure and Characterization of the Coordination Polymer [Ni2(2-mpac)4(4,4'-bpy)·2H2O]n

Utilizing mononuclear complex Ni(2-mpac)2(H2O)2 as the molecular building block,a novel coordination polymer [Ni2(2-mpac)4(4,4'-bpy)·2H2O]n (1,2-mpac = 5-methyl-2-pyrazinecarboxylic acid, 4,4'-bpy = 4,4'-bipyridine) was successfully synthesized and structurally characterized by X-ray single-crystal diffraction method. Crystal data: monoclinic, space group C2/c, a = 23.870(1),b = 9.887(4), c = 18.929(9) (A),β= 126.840(5)°, V = 3575(3) (A)3, Z = 4, S = 1.046, μ = 1.594 mm-1,F(000) = 1768 and Dc = 1.127 g·cm-3. The final R = 0.0351 and wR = 0.0792 for 2372 observed reflections with Ⅰ＞ 2σ(Ⅰ) and R = 0.0564 and wR = 0.0938 for all reflections.     

Synthesis and Crystal Structure of a [Cu(HTren)Cl2]ClO4·H2O Complex (Tren = Tris(2-aminoethyl)amine)

The title complex [Cu(HTren)Cl2]ClO4·H2O (Tren = tris(2-aminoethyl)amine) was crystal (CuC6H21Cl3N4O5) is of triclinic, space group P-1, with a = 8.2689(2), b = 8.4503(3), c=11.6801(4)(A), a = 96.9350(10), β= 108.2440(10), γ = 90.7550(10)°, V= 768.32(4)(A)3, Z= 2, Mr=399.16, Dc= 1.725 g/cm3,μ= 1.962 mm-1, F(000) = 410, T= 293(2) K, the final R = 0.0479 and wR = 0.1339 for 2659 observed reflections with I ＞ 2σ(I). X-ray single-crystal structure analysis reveals that the copper(Ⅱ) atom adopts a slightly distorted square-pyramidal geometry. The distances between Cu and N atoms (N(1), N(2), N(3)) range from 1.975(4) to 2.116(3)(A). The bond lengths of Cu-Cl(1) and Cu-Cl(2) are 2.309(10) and 2.591(10) (A), respectively. The whole crystal presents a three-dimensional network structure by hydrogen bonds.     

Gas phase reactions of Cl2O with X−(D2O)n=0–4 (X = O,OD, O2, DO2, and O3)

The reactions of Cl₂O with the cluster ions X⁻(D₂O)_n=0–4 (X = O, OD, O₂, DO₂, and O₃) were studied in a He buffer gas at temperatures within the range 171–298 K and pressures of 0.27–0.51 Torr, using a flow-tube apparatus. All ions were found to react with Cl₂O at rates slower than predicted by the collision rate and the charge center was transferred from X⁻ to Cl⁻ or ClO⁻. The primary product ions Cl⁻(DOCl) and ClO⁻(DOCl) were observed to react further to produce the ions Cl₃O⁻ and Cl₃O₂⁻. The rate constants for the observed reactions are reported and the role that thermodynamics plays in determining possible reaction channels is discussed.     

层状金属配位聚合物[｛NIX_2(bipy)｝n](X=F,Cl,Br,I;bipy=4,4'-bipyridyl)的能带结构研究

用紧束缚（EHT）晶体轨道方法对层状金属配住聚合物[{Nix2。（bipy）｝n]（X=F，Cl，Br，I；bipy=4，4’－bipyridyl）进行了能带结构计算，并利用键向量方法对这一系列聚合物能带特征和成键性质进行了讨论。研究表明，Fermi能级附近的能带主要是金属镍原子和卤素原子之间形成的d－pσ反键作用，这一反键作用的强弱对导电性起决定作用。