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1.
A mixed complex [Zn(C5H6N2)(HL)2] (C5H6N2 = 2-aminopyridine, H2L = acetyl- acetone) has been synthesized and characterized by IR, elemental analysis and X-ray single-crystal diffraction analysis. The crystal belongs to monoclinic, space group P21/c with a = 7.4490(15), b = 8.2650(17), c = 27.615(6)(A),β = 101.69(3)°, V = 1664.9(6)(A)3, Z = 4, Mr = 357.70, Dc = 1.427 g/cm3, F(000) = 744, μ = 1.493 mm-1, R = 0.0309 and wR = 0.0771. The Zn(II) is coordinated by one nitrogen atom from 2-aminopyridine and four oxygen atoms from two acetylacetone anions to furnish a distorted square pyramid geometry. The complex forms a three-dimensional network through intermolecular hydrogen bonds. 相似文献
2.
Rodríguez-Laguna Norma Reyes-García Luis Ignacio Pacheco-Gómez Raúl Flores Raúl Rojas-Hernández Alberto Gómez-Balderas Rodolfo 《Journal of Thermal Analysis and Calorimetry》2019,136(4):1701-1709
Journal of Thermal Analysis and Calorimetry - In this work, a thermodynamic study of the Zn(II)/L systems (L??=?acetate, AcO? or indomethacin anion, Indo? or... 相似文献
3.
A new dimeric compound, [Zn(bpdc)(L)]2·4H2O(1, L = 11-fluoro-dipyrido[3,2-a:2',3'-c]phenazine and bpdc = 1,1'-biphenyl-2,2'-dicarboxylate), has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction. It crystallizes in monoclinic, space group C2/c with a = 23.671(5), b = 22.547(5), c = 13.741(3), β = 123.47(3)o, V = 6118(2) 3, Z = 4, C66H44Cl2F2N8O12Zn2, Mr = 1380.73, Dc = 1.499 g/cm3, F(000) = 2816, μ(MoKa) = 0.949 mm-1, R = 0.0572 and wR = 0.1620. In 1, Zn1 and the symmetry formed Zn1 ions are connected by four bridging bidentate carboxylate groups from two independent bpdc anions to yield a binuclear unit with the Zn···Zn separation by bpdc anions of 4.168. Two L ligands are located on both sides of the dimer in chelating bidentate modes. The lateral L ligands from neighboring dimers are paired through strong π-π interactions to result in a fascinating 1D ladder-like supramolecular array. In addition, neighboring supramolecular ladders are packed each other to yield a 3D supramolecular architecture with a 1D channel. 相似文献
4.
《Polyhedron》2002,21(12-13):1279-1288
The crystal structures of two mono(dpyam)copper(II) complexes, [Cu(dpyam)(NO2)2] (1) and [Cu(dpyam)(H2O)2(SO4)] (2) and two dithiocyanate compounds containing bis(dpyam)copper(II) units, [Cu(dpyam)2(NCS)](SCN)·0.5DMSO (3) and [Cu(dpyam)2(SCN)2] (4) have been determined by X-ray crystallography. The second orthorhombic form of the monomeric Cu(II) complex 1 was obtained by the reaction of di-2-pyridylamine (dpyam) with CuCl and NaNO2 in water–methanol solution. Each copper(II) ion in 1 exhibits a tetrahedrally-distorted square base of the CuN2O2 chromophore, with off-the-z-axis coordinated nitrito groups weakly bound in approximately axial positions. Complex 2 is an example of a polymeric copper(II) derivative containing the bidentate bridging sulfate ligand in the long-bonded axial positions. Each copper(II) ion in 2 shows an elongated tetragonal octahedral stereochemistry. The CuN4N′ chromophore of 3 involves a square-based pyramidal structure, slightly distorted towards a trigonal bipyramidal stereochemistry, τ=0.13. One of the SCN− anions is bonded to the copper(II) ion via the N atom in the axial position of the square pyramid. Complex 4 is centrosymmetric and octahedrally elongated, with the SCN− anions coordinating in axial positions via the S atom. The structures of complexes 1–4 and their ESR and electronic reflectance spectra are compared with those of related complexes. 相似文献
5.
The redox behavior of [Zn(dmit)2]2- and its electrodeposited film were investigated by cyclic voltammetry, and the Ⅰ-Ⅴ properties of the electrodeposited film were measured. The results show that [Zn(dmit)2]2- possesses good redox switch properties which exhibit good repeatability. It could be considered as a new material for molecular switch and memory. 相似文献
6.
IntroductionTheabilityofdithiocarbamate(dtc)bindingtometalshasbeenknownformanyyears .Itformschelateswithvirtu allyalltransitionmetals.1Thebidentateanionisalsowellknownasabridgebetweentwotransitionmetalcenters.2 Wa ter solubledialkyldithiocarbamatecomplexes… 相似文献
7.
A new Zn(Ⅱ) complex, [Zn(L)(IPP)(H2O)]·2H2O(1, H2 L = 3-carboxy-1-carboxymethyl-2-oxidopyridinium and IPP = 2-(1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)phenol), was synthesized under hydrothermal conditions and its structure was determined by single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 8.5023(17), b = 9.945(2), c = 15.573(3) ?, α = 95.87(3), β = 102.56(3), γ = 100.73(3)o, V = 1248.7(4) ?3, Z = 2, C27H22N5O9 Zn, Mr = 625.87, Dc = 1.665 g/cm3, F(000) = 642, μ(Mo Ka) = 1.053 mm-1, R = 0.0474 and w R = 0.1352. In 1, one L2-, one IPP and one water molecule coordinate to the same Zn(II) atom to give a discrete complex with two lattice water molecules. Adjacent [Zn(L)(IPP)(H2O)]·2H2O molecules interact through π-π stacking between two IPP ligands to form a supramolecular chain. The N–H···O and O–H···N hydrogen bonds further stabilize the supramolecular chain structure of 1. The solid state luminescent property of 1 was also studied. 相似文献
8.
A new Zn(Ⅱ) complex,[Zn(1,2,3-HBTC)(L)]2(1,L = 2-(2-chloro-6-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline and 1,2,3-H3 BTC = 1,2,3-benzentricarboxylic acid),was synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction.It crystallizes in triclinic,space group P1 with a = 10.455(2),b = 11.533(2),c = 12.499(3) ?,α = 116.97(3),β = 94.08(3),γ = 103.29(3)o,V = 1280.2(4) ?3,Z = 1,C56H28Cl2F2N8O12Zn2,Mr = 1244.50,Dc = 1.614 g/cm3,F(000) = 628,μ(Mo Ka) = 1.124 mm-1,R = 0.0502 and w R = 0.1417.In compound 1,two 1,2,3-HBTC anions bridge two Zn(Ⅱ) atoms to give a dimeric structure with Zn···Zn distance of 3.15 ?.Adjacent dimers interact through π-π stackings between two L ligands to result in a supramolecular layer.Moreover,N–H···O and O–H···N hydrogen bonds further stabilize the 2D supramolecular architecture of 1.In addition,the luminescent property of 1 has been studied. 相似文献
9.
S. A. Novikov E. V. Peresypkina L. B. Serezhkina A. V. Virovets V. N. Serezhkin 《Russian Journal of Inorganic Chemistry》2014,59(2):63-71
[[UO2(L)(OH)] (I), (CN3H6)2[(UO2)2CrO4(L)4] · 2H2O (II), and [UO2(H2O)5][(UO2)2Cr2O7(L)4] (III) crystals, where L is picolinate ion C5H4NCOO?, have been synthesized and studied by X-ray diffraction and IR spectroscopy. Complex I crystallizes in triclinic system with the unit cell parameters a = 6.2858(5) Å, b = 7.9522(5) Å, c = 8.3598(6) Å, α = 79.527(6)°, β = 87.760(6)°, γ = 79.126(6)°, space group P $\bar 1$ , Z = 2, R = 0.0306, and complexes II and III crystalize in monoclinic system with a = 8.8630(9) Å, b = 13.4540(13) Å, c = 31.266(3) Å, β = 93.118(3)°, space group C2/c, Z = 4, R = 0.0187 (II), and a = 7.3172(4) Å, b = 15.4719(8) Å, c = 16.6534(10) Å, β = 98.943(4)°, space group P21/m, Z = 2, R = 0.0588 (III). The structure of complex I is built of electronegative [UO2(L)(OH)] chains, which belong to the AT11M2 crystallochemical group (A = UO 2 2+ , T11 = L, M2 = OH?) of uranyl complexes. The structure of complexes II and III contains [(UO2)2(L′)(L)4]2? dimers (L′ = CrO 4 2? or Cr2O 7 2? ), which belong to the A2B2B 4 01 group (A = UO 2 2+ ,B2 = L′, B01 = L). The specifics of intermolecular interactions in the structures of complexes I–III and some their analogues have been considered using molecular Voronoi-Dirichlet polyhedra. 相似文献
10.
11.
L. A. Glinskaya Z. A. Savel’eva S. N. Bizyaev A. V. Tkachev S. V. Larionov 《Journal of Structural Chemistry》2012,53(6):1111-1117
The crystal structure of a solvate [Zn(HL)Cl]·EtOH is determined by single crystal X-ray crystallography (150 K, Bruker X8 Apex CCD autodiffractometer, MoK α radiation). The crystals are triclinic, unit cell parameters are: a = 7.4755(4) Å, b = 13.9701(11) Å, c = 14.4593(19) Å, α = 82.277(2)°, β = 75.410(2)°, γ = 75.356(1)°, space group P1. The structure of the solvate contains two crystallographically independent complex [Zn(HL)Cl] molecules and two non-coordinated ethanol molecules. In each of the molecules, Zn2+ ions coordinate N atoms of tetradentate chelating ligands HL? and a Cl atom. ClN4 polyhedra have a distorted tetragonal pyramidal geometry. EtOH molecules make H-bonds with the complex molecules, thus facilitating the formation of chains along the x axis. 相似文献
12.
Introduction -Amino acids as additive have a wide application in medicines, foodstuff and cosmetics.1-3 The synthetic methods of amino acid have been reviewed.4,5 The solu-bility property of Zn(AcO)2-Thr-H2O (Thr=Threonine) system at 298.15 K has been investigated by the semimicro-phase equilibrium method, in which the phase region of the complex did not exist.6 The prepara-tion of Zn(Thr)SO4H2O was reported in Ref. 7∶3 times volume of acetone relative to that of water was added into t… 相似文献
13.
S. V. Larionov L. I. Myachina L. A. Glinskaya I. V. Korol’kov E. M. Uskov O. V. Antonova V. M. Karpov V. E. Platonov V. P. Fadeeva 《Russian Journal of Coordination Chemistry》2012,38(12):717-723
Compounds p-HOOCC6F4COOH · H2O (H2L · H2O), [Tb2(H2O)4(L)3 · 2H2O] n (I), and Tb2(Phen)2(L)3 · 2H2O (II) are synthesized. According to the X-ray structure analysis data, the crystal structure of H2L · H2O is built of centrosymmetric molecules H2L and molecules of water of crystallization. The crystal structure of compound I is built of layers of coordination 2D polymer [Tb2(H2O)4(L)3] n and molecules of water of crystallization. The ligands are the L2? anions performing both the tetradentate bridging and pentadentate bridging-chelating functions. The coordination polyhedron TbO9 is a distorted three-capped trigonal prism. Acid H2L manifests photoluminescence in the UV region (??max = 368 nm). Compounds I and II have the green luminescence characteristic of the Tb3+ ions, and the band with ??max = 545 nm (transition 5 D 4?? 7 F 5) is maximum in intensity. The photoluminescence intensity of compound II is higher than that for compound I. 相似文献
14.
The reaction of 1-phenacylimidazole with W(CO)6 in a 1:1 molar ratio under irra- diation with a high-pressure Hg lamp mainly yielded the title compound (C29H26N4O7W, Mr = 726.39), which is of orthorhombic, space group Pbca with a = 27.665(4), b = 7.7807(12), c = 27.803(4) (A), V = 5984.8(16) (A)3, Z = 8, Dc = 1.612 g/cm3, λ(MoKα) = 0.71073 (A), μ = .3.911 mm-1, F(000) = 2864, R = 0.0583 and wR = 0.1502 for 3356 observed reflections (I > 2σ(I)). The crystal structural analysis indicates that in the coordination geometry of tungsten, 1-phenacylimidazole acts as a monodentate ligand and two imidazole ligands locate in a cis-position. 相似文献
15.
Wei S Peng J Wang M Fang X Fan Y Li X Lu J 《Chemical communications (Cambridge, England)》2012,48(38):4615-4617
The (Zn(0.95)Mn(0.05)S)(2)·L (L = hexylamine and octylamine) hybrids show the optimal Mn(2+) luminescence and their thin films were fabricated on the quartz substrate layer by layer by a spin coating method, which revealed the linear relationship of the UV optical absorption and the Mn(2+) luminescence intensity with the layer numbers. 相似文献
16.
《Journal of Coordination Chemistry》2012,65(15):2649-2657
A series of binuclear Schiff-base complexes of zinc(II) and mercury(II) containing bidentate ligands (HL) [HL?=?salicylidene-2-methyl-1-aminobenzene (HL1), salicylidene-2-aminopyridine (HL2), and salicylidene-3-nitro-1-aminobenzene (HL3)] with “N” and “O” donors have been synthesized by simple metathetic reactions of anhydrous metal chlorides with sodium salts of Schiff bases (in tetrahydrofuran (THF)/MeOH) in equimolar ratio to produce [(µ-Cl)2M2(L)2?·?xTHF] [where M?=?Zn(II) and Hg(II); L?=?HL1, HL2, and HL3; x?=?0 for (1), (4), (6) and x?=?2 for (2), (3), (5)]. The main emphasis on the complexes [(µ-Cl)2M2(L)2?·?2THF] (2), (3), and (5) is given due to their five-coordinate environment around metal ions. The complexes have been characterized by elemental analyses (M, Cl, C, H, N), melting point, and spectral (FT-IR, 1H-NMR, and 13C-NMR) studies. The structural composition of the complexes has been determined by FAB-MS spectral studies. FAB-MS showed the isotopic molecular ion peak [M+] and fragments supporting the formulation. Powder X-ray diffraction study of 6 is also reported showing the crystallite size (404.5?Å) of the complex. 相似文献
17.
A new complex Zn(Ⅱ)L2·2CH3OH(H2L = 4-chloro-2-(2,3-dihydro-1H-ben-zoimi-dazol-2-yl)-phenol) has been prepared and characterized by single-crystal X-ray diffraction analysis and elemental analysis.The crystal is of triclinic system,space group P1 with a = 9.2905(10),b = 10.3555(13),c = 14.9590(14) ,α = 101.0340(10),β = 101.261(2),γ = 99.1660(10)o,V = 1356.1(3) 3,Z = 2,C28H24Cl2N4O4Zn,Mr = 616.78,Dc = 1.510 g/cm3,μ = 1.145 mm·1,F(000) = 632,the final R = 0.0379 and wR = 0.0830 for 3606 observed reflections with I 2σ(I).The Zn(Ⅱ) atom presents a distorted square pyramidal coordination involving two H2L ligands.The hydrogen bonds and π···π stacking interactions extend the complex into a two-dimensional framework. 相似文献
18.
《Journal of Coordination Chemistry》2012,65(5):427-431
A new dinuclear Cd(II) complex, [L2Cd2(μ-N3)2(N3)2], containing two end-on bridging azide ligands, two monodentate N3 ligands and 1,4,7-triazacyclononane as the capping ligand, has been synthesized and its structure determined by X-ray crystallography. The complex crystallizes in the monoclinic space group P21/c with a=8.467(3), b=14.359(5), c=10.115(4)Å, β=95.026(6)° and z=4. The cadmium(II) centre is six-coordinate with distorted octahedral geometry, bonded to three N atoms of the 1,4,7-triazacyclononane, two nitrogen atoms of μ-azide bridges and one nitrogen atom of a monodentate azide ligand. Neighboring Cd(II) atoms are linked by the double end-on azide bridges. 相似文献
19.
A novel sensitizer with imidazole zinc porphyrin as electron donor has been synthesized. The structure has been characterized by UV-Vis, elemental analyses and 1 H NMR.UV-Vis and fluorescence spectra show that it has good light absorbing properties in the range of visible light and suggests that it has potential applications in dye-sensitized solar cells. 相似文献
20.
L. Mei L. S. Tai J. Li F. H. Tao L. X. Liang Y. S. Zhong 《Russian Journal of Coordination Chemistry》2011,37(2):153-159
Compound I, [di-μ-methoxo-bis[(2-aminopyridine)(chloro)copper(II)], was obtained by two different synthetic routes. In synthetic route 1, we first obtained intermediate by the addition of two equivalents of o-aminopyridine to copper chloride in an ethanolic solution, and then we recrystallized the intermediate from methanol and n-hexane to give compound I. Synthetic route 2 involved the reaction of o-aminopyridine with copper chloride in a methanol solution directly. The crystal structure of compound I was obtained. The reaction of m-xylylenediamine with Zn(OAc)2 · 2H2O in THF resulted in the production of one novel zinc complex C12H18N2O4Zn, bis(m-xylenediamine)zinc (II) and its structure was determined by X-ray diffraction analysis. Complexes I and II were also characterized by elemental analysis, and IR. Then they were applied as catalysts for the Henry reaction, and they achieved good conversions (64 and > 99%, respectively). 相似文献