Crystal and molecular structure of the tetracyanato-bis(phenanthroline)copper(II) complex

1991 ◽  
Vol 56 (8) ◽  
pp. 1601-1606 ◽  
Author(s):  
Kim Tae Jin ◽  
Mária Kabešová ◽  
Josef Kožíšek

At room temperature, the [Cu2(NCO)4(phen)2] complex possessed monoclinic symmetry, P21/n, with the unit cell parameters a = 0.7757(3) nm, b = 1.3563(5) nm, c = 1.1555(4) nm, β = 96.92(2)°, Z = 2. The central atom is involved in tetragonal pyramidal coordination comprising the CuN4Cu’ chromophor. The nitrogen atoms of the cyanate and phenanthroline ligands are in a square planar arrangement, from which the central copper atom is displaced in the axial direction. Through the Cu-Cu bond (0.320 nm), the [Cu(NCO)2(phen)] formula units are linked into centrosymmetric units, which in the crystal structure lie in parallel layers. The occurrence of the Cu-Cu bond can account for the fact that only one molecule of the heterocyclic ligand can be coordinated.

1989 ◽  
Vol 54 (7) ◽  
pp. 1800-1807 ◽  
Author(s):  
Mária Kabešová ◽  
Zlatica Kožíšková

Crystals of the complexes [Cu(3,4-diMepy)3(NCS)2] (I) and [Cu(3-Mepy)3(NCS)2] (II) (Me = methyl, py = pyridine) possess the monoclinic symmetry, Pc, with the unit cell parameters of I and II: a = 0.9825(7) and 0.9027(7) nm, b = 0.9740(7) and 0.9021(7) nm, c = 1.4130(60) and 1.4958(50) nm, β = 108.8(4)° and 114.08(4)°, Z = 2 in both cases, d0 = 1.32.103 and 1.37.103 kg m-3, and dc = 1.30.103 and 1.37.103 kg m-3, respectively. The central atom in the complexes exhibits tetragonal pyramidal coordination. The thiocyanate ligands are coordinated by the nitrogen atoms in the equatorial as well as axial positions of the coordination polyhedron. The three heterocyclic ligands are bonded in the equatorial plane. The arrangement of the ligands and the interatomic distances are the same in the two complexes. The crystals were prepared by reacting an ammoniacal solution of CuSO4 with an ethanolic solution of the heterocyclic ligand L and an aqueous solution of NH4NCS so that the c(Cu):c(NH3):c(L):c(NCS) ratio was 2:8:5:4.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1692-C1692
Author(s):  
Graciela Díaz de Delgado ◽  
Belkis Ramírez V. ◽  
William Velásquez ◽  
Julio Trejo Dávila ◽  
Chun-Hsing Chen ◽  
...  

The need for improving the description of structural features with better quality data, at low temperature and with modern 2D detectors of certain materials, sometimes leads to surprisingly new insights into a previously reported structure. When attempting to grow single crystals of maleamic acid, good crystals of ammonium maleate, NH4(Mal), were obtained. Although the structure of this material has been reported at room temperature, in space group Pbcm with V=613.2(5) Å3[1], synchrotron data were collected at low temperature to examine the behavior of the ammonium moiety. The data collected lead to a structure better described in Pbca, a=8.9687(12), b=8.1604(8), c=16.348(2) Å, V=1196.5(2) Å3, Z=8. The refinement converged to R=0.0438, wR2=0.1156, S=1.02. An examination of the new data indicates that reflections with h odd are systematically weak but, nevertheless, present. The Ca derivative of valproic acid (a common anticonvulsant) was reported as monoclinic, C2/c, with a=16.250(8), b=18.471(17), c=7.729(7) Å, β=109.71(5)0, V=2183.97 Å3, Z=4, and R=10.94% [2]. However, data collection at room temperature and under a stream of nitrogen on several newly prepared crystals always lead to a triclinic, P-1 cell, with approximately half the volume of the reported cell. Attempts to index the dataset using the known monoclinic cell resulted in high uncertainties for the unit cell parameters and high Rint values since reflection spots showed splitting and diffuse scattering. The new cell had dimensions a=7.6995(4) Å, b=11.7444(6) Å, c=11.7708(6) Å, α=91.089(3)0, β=101.643(3)0, γ=102.041(3)0, V=1017.47(99) Å3, Z=2. Although the initial refinement was discouraging (R=0.1172, wR2=0.360, S=1.12) the analysis with PLATON indicated the presence of twining and, after considering the twin law, the refinement improved significantly (R=0.059, wR2=0.1472, S=0.99). Several examples where a new data collection resulted in interesting results will be presented.


2005 ◽  
Vol 60 (11) ◽  
pp. 1149-1157 ◽  
Author(s):  
Matthias Siebold ◽  
Alexandra Kelling ◽  
Uwe Schilde ◽  
Peter Strauch

Planar bis(1,2-dithiooxalato)nickelates(II) react in aqueous solutions of lanthanide ions to form pentanuclear, heterobimetallic complexes of the general composition [{Ln(H2O)n}2- {Ni(dto)2}3]・xH2O (Ln = Y3+, La3+, Ce3+, Pr3+, Nd3+, Sm3+, Eu3+, Gd3+, Tb3+, Dy3+, Ho3+, Er3+, Tm3+, Yb3+, Lu3+; n = 4 or 5; x = 9 - 12). With [{Nd(H2O)5}2{Ni(S2C2O2)2}3]・xH2O (x = 10 - 12) (1) and [{Er(H2O)4}2{Ni(S2C2O2)2}3]・xH2O (x = 9 - 10) (2) we were able to isolate two complexes of this series as single crystals, which were characterized by X-ray structure analysis. Depending on the individual ionic radii of the lanthanide ions, the compounds crystallize in two different crystal systems with the following unit cell parameters: 1, monoclinic in P21/c with a = 11.3987(13), b = 11.4878(8), c = 20.823(2) Å , β = 98.907(9)° and Z = 2; 2, triclinic in P1̅ with a = 10.5091(6), b = 11.0604(6), c = 11.2823(6) Å , α = 107.899(4)°, β = 91.436(4)°, γ = 112.918(4)° and Z = 1. The channels and cavities appearing in the packing of the molecules are occupied by uncoordinated water molecules. High magnetic moments up to 14.65 BM./f.u. have been observed at room temperature due to the combined moments of the individual lanthanide ions.


2007 ◽  
Vol 63 (3) ◽  
pp. o1464-o1466 ◽  
Author(s):  
Wiesław Prukała ◽  
Bogdan Marciniec ◽  
Maciej Kubicki

The crystal structure of tetra-n-butylammonium iodide, C16H36N+·I−, has been redetermined at room temperature and at 100 (1) K. In the low-quality (R = 0.142) room-temperature determination by Wang, Habenschuss, Xenopoulos & Wunderlich [Mol. Cryst. Liq. Cryst. Sci. Technol. Sect. A (1995), 264, 115–129], this structure was described as crystallizing in the space group C2 with Z′ = 2. Our results prove that the correct space group is C2/c (with the same unit-cell parameters as in the original determination) at both temperatures. In the crystal structure, the iodide anions fill the voids in the grid-like cationic structure. Weak C—H...I interactions (eight per anion) strengthen this packing.


2010 ◽  
Vol 74 (3) ◽  
pp. 433-440 ◽  
Author(s):  
C. H. Yoder ◽  
E. Bushong ◽  
X. Liu ◽  
V. Weidner ◽  
P. McWilliams ◽  
...  

AbstractSyntheses for the three members of the copper hydroxyl nitrate family – the polymorphs rouaite and gerhardtite, and likasite – are presented along with powder diffraction data and unit-cell parameters. The solubilities, determined in 0.05 M KNO3solution after equilibration at 25°C for 10 days were used to calculate activity-based solubility product constants. The Gibbs energies of formation, obtained from the solubility products, are –653.2±0.7 kJ/mol, –655.1±1.2 kJ/mol and –1506.4±1.1 kJ/mol, for rouaite, gerhardtite, and likasite (Cu3NO3(OH)5·2H2O), respectively. The values for the polymorphs rouaite and gerhardtite validate the observations of Oswald that gerhardtite is the most stable polymorph at room temperature and that the preparation of predominantly rouaite in syntheses carried out at room temperature must be due to the metastability and low rate of conversion to the more stable gerhardtite.


2008 ◽  
Vol 72 (3) ◽  
pp. 771-783 ◽  
Author(s):  
L. Bindi ◽  
M. D. Welch ◽  
P. Bonazzi ◽  
G. Pratesi ◽  
S. Menchetti

AbstractThe crystal structure of seeligerite, Pb3IO4Cl3, from the San Rafael mine, Sierra Gorda, Chile, was solved in the space group Cmm2, and refined to R = 3.07%. The unit-cell parameters are: a = 7.971(2), b = 7.976(2), c = 27.341(5) Å, V = 1738.3(6) Å3 and Z = 8. The crystal structure consists of a stacking sequence along [001] of square-net layers of O atoms and square-net layers of Cl atoms with Pb+ and I+ cations located in the voids of the packing. As is typical of cations with a stereoactive lone-pair of electrons, Pb2+ and I5+ adopt strongly-asymmetrical configurations. Pb2+ cations occur in a variety of coordination polyhedra, ranging from anticubes and monocapped anticubes to pyramidal ‘one-sided’ coordinations. I5+ is coordinated by a square of four oxygen atoms: I1 and I3 exhibit a ‘one-sided’ coordination, whereas I2 has square-planar coordination.The TEM investigation has revealed additional superlattice reflections (which were not registered by X-ray diffraction (XRD)) in the hk0 diffraction pattern of seeligerite based upon a 0.158 Å-1 square net, which can be interpreted as arising from a 20-cation super-sheet motif (12.6 Å x 12.6 Å), likely related to a further level of Pb-I order superimposed upon the 8-site motif identified by XRD.


1982 ◽  
Vol 47 (2) ◽  
pp. 409-420 ◽  
Author(s):  
Viktor Vrábel ◽  
Ján Garaj

The crystal structure of [Cuen2(NO3)]SeCN was solved by the single-crystal X-ray structural analysis method. The compound crystallizes in the monoclinic system with space group Pc. The unit cell has dimensions: a = 0.9254(3), b = 1.4018(3), c = 0.9722(5) nm, β = 99.20(3)°. The structure was refined by the least squares method to a final value of R = 6.8% for 1965 observed reflections. The crystal structure consits of polymeric cation chain [Cuen2(NO3)]+ and of free uncoordinated SeCN- anions. The nitrate ion NO-3 forms a bridging unit between two [Cuen3]2+ cations. The coordination polyhedron around the Cu(II) atom is a deformed octahedron, formed of two ethylendiamine molecules and two oxygen atoms of the NO-3 ions, bonded to divalent copper in the axial direction along the long coordinates. The crystal structure contains selenocyanate which is not bonded through a covalent bond to the central atom, but there are intermolecular contacts with its immediate surroundings.


1999 ◽  
Vol 14 (4) ◽  
pp. 280-283 ◽  
Author(s):  
A. Rafalska-Łasocha ◽  
W. Łasocha ◽  
M. Michalec

The X-ray powder diffraction patterns of anilinium trimolybdate tetrahydrate, (C6H5NH3)2Mo3O10·4H2O, and anilinium trimolybdate dihyhydrate, (C6H5NH3)2Mo3O10·2H2O, have been measured in room temperature. The unit cell parameters were refined to a=11.0670(7) Å, b=7.6116(8) Å, c=25.554(3) Å, space group Pnma(62) and a=17.560(2) Å, b=7.5621(6) Å, c=16.284(2) Å, β=108.54(1)°, space group P21(4) or P21/m(11) for orthorhombic anilinium trimolybdate tetrahydrate and monoclinic anilinium trimolybdate dihydrate, respectively.


A complex consisting of one molecule of 5-bromouridine ( BUR ) and one molecule of di­methylsulphoxide ( DMSO ) has been prepared in the form of monoclinic crystals. The unit cell parameters are as follows, a = 13⋅65 ± 0⋅01, b = 4.820 ± 0⋅005, c = 12⋅09 ± 0⋅01 Å, β = 91⋅8 ± 0.1°, space group P 2 1 . X-ray diffraction data ( ⋋ = 1⋅5418 Å) for 1389 independent reflexions were collected and the structure was determined from Patterson syntheses which gave the coordinates of the bromine and sulphur atoms. Fourier syntheses followed by least-squares refinement (including anisotropic temperature parameters) reduced the agreement index R to 0⋅067. The bond lengths and angles for each molecule are given, and it is shown that hydrogen bonds are formed between the oxygen atom of the DMSO molecule and the 03' and 05' of the BUR molecules. A comparison is made between the conformation of the BUR molecule in this complex and that of the same molecule in two other structures.


2000 ◽  
Vol 55 (3-4) ◽  
pp. 238-242 ◽  
Author(s):  
A. B. M. Shamsur Rahman ◽  
H. Boiler ◽  
K. O. Klepp

Abstract Red-brown crystals of a new bis(thiomolybdate) complex [Me4N]3[(MoOS3)2Ag] were formed at room temperature through the reaction of a solution of [Me4N]2[MoOS3] in MeCN with solid AgCN. They are monoclinic, space group P21/c with unit cell parameters a = 16.662(9), b = 9.464(3), c = 17.890(8) A, /3 = 101.87(2)°, Z = 4. The crystal structure was determined from single crystal diffractometer data (MoKα-radiation) and refined to R = 0.044 (3614 reflections, 236 variable parameters). The structure is characterized by trinuclear complex anions, [(MoOS3)2Ag]3-. According to Weissenberg investigations the homologous tungsten compound is isostructural. The infrared spectrum of the molybdenum complex (KBr powder) shows absorption bands at 884 (vs) and 871 (w) cm-1 (terminal v(Mo-0)), 483 (vs) cm-1 (terminal v(Mo-S)), 451 (vs), and 435 (w) cm-1 (bridging v(Mo-S)). The tungsten complex showed bands at 901 (vs) cm-1 (terminal v(W-O)), 478 (vs) cm-1 (terminal v(W-S)), and 435 (vs) cm-1 (bridging v(W-S)). The anionic mass spectra shows molecular ion peaks at m/z 524 and 700 for [(MoOS3)2Ag]- and [(WOS3)2Ag]-, respectively, as well as peaks for other fragments.


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