Crystal structures of nickel(II) and copper(Il)-Schiff-bases complexes with tetramic and tetronic acid subunits

1994 ◽  
Vol 209 (12) ◽  
Author(s):  
G. Reck ◽  
B. Schulz ◽  
A. Zschunke ◽  
O. Tietze ◽  
J. Haferkorn
Keyword(s):  
Complex Formation ◽  
Water Molecule ◽  
Crystal Structures ◽  
Schiff Bases ◽  
Water Molecules ◽  
Ligand Molecule ◽  
Tetragonal Pyramid ◽  
Space Group ◽  
Tetronic Acid ◽  
Oxygen Ligand

AbstractN,N′-ethylene-bis-(tetronic-acid-3-formiminato)-copper(II)/K1 crystallizes in space groupN,N′-ethylene-bis-(tetronic-acid-3-formiminato)-nikkel(II)/K2 crystallizes in space groupN,N′-ethylene-bis-(1,5,5-trimethyltetramic-acid-3-formiminato)-copper(II)/K3 crystallizes in space groupIn K1 and K3 copper is coordinated by two nitrogen and two oxygen atoms of the ligand molecule as well as by one water molecule on top of a tetragonal pyramid. In K2 two water molecules are included in the complex formation. These and two nitrogen as well as two oxygen ligand atoms form a nearly regular octahedron.

The crystal structures of potassium Tris(oxalato)-chromate(III) and -aluminate(III) trihydrate: A reinvestigation

1978 ◽  
Vol 31 (7) ◽  
pp. 1455 ◽  
Author(s):  
D Taylor
Keyword(s):  
Water Molecule ◽  
Least Squares ◽  
Crystal Structures ◽  
Three Dimensional ◽  
Water Molecules ◽  
Intensity Data ◽  
Hydrogen Atoms ◽  
Space Group ◽  
Fourier Techniques ◽  
Difference Fourier

The crystal structures of the isomorphous complexes K3 [M(oxalate)3],3H2O, M = CrIII and AlIII, have been determined from three- dimensional diffractometer intensity data by conventional Patterson and difference Fourier techniques. The crystals are monoclinic; M = Cr, a 7.714(1), b 19.687(4), c 10.361(2) Ǻ, β 108.06(3)�; M = Al, a 7.712(1), b 19.518(3), c 10.286(2) Ǻ, β 108.21(3)�; space group P21/c with Z = 4. Block-diagonal least-squares refinement of all non-hydrogen atoms con- verged at R 0.040, Rw 0.051 (M = Cr); R 0.048, Rw 0.056 (M = Al). The structures are comprised of discrete M(ox)33- anions, K+ cations and water molecules. One potassium ion and one water molecule appear to be cooperatively disordered over two possible pair sites (α, β) with occupancy ratios α/Ǻ c. 3 : 1. The geometries within the M(ox)33- anions are as expected with <Cr-O> 1.969(13), <Al-O> 1.896(15) Ǻ. The oxalate ligands are non-planar with <C-O(inner)> 1.284(6), 1.279(12); <C-O(outer)> 1.223(5), 1.223(10) and <C-C> 1.538(16), 1.534(21) Ǻ for the two structures.

Studies in aryltin chemistry. Part 6. Crystal and molecular structures of tetra(p-methylsulphonylphenyl)tin(IV) and tetra(p-methylsulphinylphenyl)tin(IV) monohydrate

1990 ◽  
Vol 68 (8) ◽  
pp. 1277-1282 ◽  
Author(s):  
Ivor Wharf ◽  
Michel G. Simard ◽  
Henry Lamparski
Keyword(s):  
Least Squares ◽  
Crystal Structures ◽  
Direct Method ◽  
Molecular Structures ◽  
Water Molecules ◽  
Monoclinic Space Group ◽  
Molecular Symmetry ◽  
Asymmetric Unit ◽  
Full Matrix ◽  
Space Group

Tetrakis(p-methylsulphonylphenyl)tin(IV) and tetrakis(p-methylsulphinylphenyl)tin(IV) n-hydrate have been prepared and their spectra (ir 1350–400 cm−1; nmr, 1H, 13C, 119Sn) and X-ray crystal structures are reported. The first compound is monoclinic, space group C2/c, Z = 4, with a = 21.589(6), b = 6.207(3), c = 22.861(11) Å, β = 93.80(3)° (22 °C); the structure was solved by the direct method and refined by full-matrix least squares calculations to R = 0.043 for 2755 observed reflections. It has 2 molecular symmetry with the methyl group and one oxygen atom completely disordered in both CH3S(O2) groups in the asymmetric unit. The second compound is tetragonal, space group P42/n, Z = 2, with a = b = 15.408(6), c = 6.379(2) Å (−100 °C); the structure was solved by the Patterson method and refined by full-matrix least squares calculations to R = 0.060 for 1209 observed reflections. It has [Formula: see text] molecular symmetry with the whole asymmetric unit disordered. Water molecules occupy positions on parallel 42 axes but molecular packing requirements prevent all sites having 100% occupancy giving n ~ 1 for the hydrate. Keywords: Tetra-aryltins, crystal structures, sulphone, sulphoxide, hydrogen-bonding.

scholarly journals Kristallstrukturen zweier Kupfer(II)-Cyclam-Komplexe: [{CuCl(C10N4H24)}2][CdCl4] und [Cu(C10N4H24)][CdCl3(H2O)2]Cl / Crystal Structures of Two Copper(II) Cyclam Complexes: [{CuCl(C10N4H24 )}2][CdCl4] and [Cu(C10N4H24)][CdCl3 (H2O)2]Cl

1995 ◽  
Vol 50 (5) ◽  
pp. 828-832 ◽  
Author(s):  
Joachim Pickardt ◽  
Isabella Hoffmeister
Keyword(s):  
Crystal Structures ◽  
Copper Atom ◽  
Water Molecules ◽  
Cadmium Atom ◽  
Bridging Ligands ◽  
Chlorine Atoms ◽  
Space Group ◽  
Distorted Octahedra ◽  
Cyclam Complexes

Abstract Crystals of both complexes were obtained by evaporation of the ethanol solvent. The crystals of [{CuCl(C10N4H24)}2][CdCl4] are tetragonal, space group I4̄2d, Z = 4, a = b = 1784.1(11), c = 1101.1(8) pm. Each copper atom is bonded to one cyclam ligand and two chlorine atoms which are acting as bridging ligands and connect the copper atoms to chains of distorted octahedra. Distorted tetrahedra of CdCl4 are situated in cavities between these chains. The crystals of [Cu(C10N4H24)][CdCl3(H2O)2]Cl are monoclinic (b), space group C2/c, Z = 4, a = 1581.9(8), b = 1323.3(7), c = 924.0(5) pm, β = 94.31(5)°. Cadmium is coordinated to four chlorine atoms and two water molecules, while all of the chlorine atoms act as bridging ligands connecting every cadmium atom to two adjacent cadmium atoms and to two copper atoms which lie in plane with the N atoms.

Komplexe mit substituierten 2,5-Dihydroxy-p-benzochinonen: Das isotype Paar BaC6X2O4 · 3 H2O (X = Cl, Br) / Complexes with Substituted 2,5-Dihydroxy-p-benzochinones: The Isotypic Pair BaC6X2O4 · 3 H2O (X = Cl, Br)

1986 ◽  
Vol 41 (12) ◽  
pp. 1495-1500 ◽  
Author(s):  
Christian Robl ◽  
Armin Weiss
Keyword(s):  
Water Molecule ◽  
Water Molecules ◽  
Topochemical Reaction ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
Oxygen Atoms

AbstractBaC6X2O4 · 3H2O (X = Cl, Br) crystallizes in the orthorhombic space group Cmca. 4 of the 8 oxygen atoms around Ba2+ belong to two different dianions, chelating Ba2+. In this way 1-dimensional corrugated chains are formed, interlinked by two oxygen atoms of neighbouring chains, thus forming layers. This interconnection is of polar character within a layer. The in­terlinking oxygen atoms have one carbon- and two Ba2+ neighbours. CN 8 is completed by two water molecules. The latter and a further water molecule situated between the layers may be removed reversibly in a topochemical reaction without destruction of the structure.

Die Kristallstrukturen von PPh4[WOCl4], (PPh4)2[WOCl5] · 2CH2CI2 und (PPh4)2[ReOCl5] · 2CH2Cl2 / The Crystal Structures of PPh4[WOCl4], (PPh4)2[WOCl5] · 2CH2CI2 and (PPh4)2[ReOCl5] · 2CH2Cl2

1984 ◽  
Vol 39 (7) ◽  
pp. 850-854 ◽  
Author(s):  
Dieter Fenske ◽  
Karlheinz Stahl ◽  
Evamarie Hey ◽  
Kurt Dehnicke
Keyword(s):  
Oxygen Atom ◽  
Chlorine Atom ◽  
Complex Space ◽  
Unit Cell ◽  
Axial Position ◽  
Formula Unit ◽  
Tetragonal Pyramid ◽  
Space Group ◽  
Oxygen Ligand ◽  
Oxygen Distance

Both tungsten compounds are formed by reaction of water and oxygen with the acetylene complex PPh4[WCl5(Ph - C ≡ C - C (Br) = C(Br) -Ph)] in CH2Cl2 solutions, and in the presence of PPh4Cl. PPh4[WOCl4] crystallizes in the tetragonal space group P4/n, with two formula units in the unit cell of dimensions a = b = 1269, c = 760 pm at -110 °C (1416 observed in dependent reflexions, R = 0 .054). The [WOCl4]⊖ ion forms a tetragonal pyramid with the oxygen ligand in axial position and a tungsten -oxygen distance of 168 pm. (PPh4)2 [WOCl5 · 2CH2Cl2 crystallizes in the tricline space group P 1̄, with one formula unit per unit cell with a = 1011, b = 1113, c = 1240 pm, α = 70.3°, β = 79.4°, γ = 80.9° at - 110 °C (3781 observed in dependent reflexions, R = 0 .087). The structure contains [WOCl5]2⊖ an ions where the oxygen atom and the chlorine atom in transposition are disordered. (PPh4)2[ReOCl5] · 2CH2Cl2 is formed by the reaction of ReCl5 with PPh4Cl in the presence of water. The compound is isotypic with the corresponding tungsten complex (space group P 1̄, Z = 1, a = 1006, b = 1109, c = 1239 pm , α = 7 0.5°, β = 79.6°, γ = 80.9° at -110 °C; 5436 observed in dependent reflexions R = 0 .050).

scholarly journals Metallkomplexe mit Guanidinderivaten als Liganden: Kristallstrukturen von [Zn(cnge)2(SCN)2] · 2H2O und Zn(eoge)Br2 (enge = Cyanoguanidin; eoge = 1-Ethoxyiminomethylguanidin) / Metal Complexes with Guanidine Derivatives as Ligands: Crystal Structures of [Zn(cnge)2(SCN)2]·2H2O und Zn(eoge)Br2 (cnge = Cyanoguanidine; eoge = 1-Ethoxyim inom ethylguanidine)

1996 ◽  
Vol 51 (10) ◽  
pp. 1469-1472 ◽  
Author(s):  
Joachim Pickardt ◽  
Britta Kühn
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Bonds ◽  
Metal Complexes ◽  
Crystal Structures ◽  
Water Molecules ◽  
Monoclinic Space Group ◽  
Intermolecular Hydrogen Bonds ◽  
Crystal Water ◽  
Space Group ◽  
Guanidine Derivatives

Crystals of |Zn(cnge)2(SCN)2]-2H2O (1) were obtained by evaporation of an aqueous solution of Z n(SO4)·7H2O , KSCN, and cyanoguanidine. Crystals of Zn(eoge)Br2 (2) were obtained by reaction of ZnBr2 and cyanoguanidine in ethanol/water. Both compounds are monoclinic, space group C2/c, 1: Z = 4, a = 1919.6(7), b = 467.3(2), c = 1838.5(6) pm, β = 112.99(3)°, 2: Z = 8, a = 1799.5(6), b = 878.7(2), c = 1367.2(5) pm, β = 101.52(3)°. In 1 each Zn is bonded to two cyanoguanidine molecules and via the N atoms to two NCS groups. Intermolecular hydrogen bonds lead to chains along the a-axis, and these chains are again connected via hydrogen bonds to the two crystal water molecules. In the course of the formation of 2, the cyanoguanidine reacted with the ethanol to form 1-ethoxyiminomethylguanidine. This ligand forms chelate rings with the Zn atoms, which are tetrahedrally coordinated by the two imino N atoms of the ligand and by two bromine atoms.

On the crystal structures of some nickel hexacyanoferrates (II,III)

2004 ◽  
Vol 19 (3) ◽  
pp. 284-291 ◽  
Author(s):  
R. Martínez-Garcia ◽  
E. Reguera ◽  
J. Balmaseda ◽  
G. Ramos ◽  
H. Yee-Madeira
Keyword(s):  
Aqueous Solution ◽  
Crystal Structures ◽  
Interstitial Water ◽  
Structural Information ◽  
Water Molecules ◽  
Ionic Exchange ◽  
Orthorhombic Distortion ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
Large Cation

The crystal structures of some nickel hexacyanoferrates (II, III), including mixed compositions containing Na+, K+ and Cs+, were resolved and refined from XRD powder patterns. Data from infrared, Mössbauer and adsorption techniques provided complementary structural information. The crystal structures of Ni3[Fe(CN)6]2⋅16H2O and NiCs2[Fe(CN)6] were refined in space group Fm3m. NiNa2[Fe(CN)6]⋅2H2O and NiK2[Fe(CN)6]⋅2H2O were found to be orthorhombic (space group Pmn21). This structure (Pmn21) results from a distortion around the alkali ion, which appears as a monohydrated interstitial species. On ionic exchange in an aqueous solution containing Cs+, the orthorhombic distortion disappears and the cubic cell is obtained. Cs+ is a large cation and space is not available for interstitial water molecules. This orthorhombic model is also supported by the Mössbauer spectra of the ferrous analogs, FeK2[Fe(CN)6]⋅xH2O and Fe[Pt(CN)6]. © 2004 International Centre for Diffraction Data.

Thermodiffractometry and crystal structures of the hexagonal-tungsten-bronze-related K3Al3F12⋅nH2O (n=2,1)

2009 ◽  
Vol 24 (4) ◽  
pp. 292-300 ◽  
Author(s):  
A. Le Bail
Keyword(s):  
Thermal Decomposition ◽  
Water Molecule ◽  
Crystal Structures ◽  
Tungsten Bronze ◽  
Space Group

K3Al3F12⋅nH2O (n=2,1) are the successive products of the thermal decomposition of K(H3O)2AlF6. Both structures are orthorhombic, built up from disconnected hexagonal-tungsten-bronze (HTB)-related layers, with K+ cations and H2O molecules inserted between. For n=2, there are two disconnected layers along a presenting different octahedra tilting [a=13.5135(2) Å, b=7.0433(1) Å, c=12.2252(2) Å, V=1163.60(3) Å3, Z=4, space group Pnma], whereas for n=1, the stacking is reduced to only one HTB layer along c [a=7.0523(5) Å, b=12.1005(9) Å, c=6.7057(5) Å, V=572.24(7) Å3 (at 170 °C), Z=2, space group Pmmn] after the departure of one water molecule. The thermodiffractometry ends in the α-KAlF4 form.

The crystal structures of sjögrenite and pyroaurite

1967 ◽  
Vol 36 (280) ◽  
pp. 465-479 ◽  
Author(s):  
L. Ingram ◽  
H. F. W. Taylor
Keyword(s):  
Crystal Structures ◽  
Three Dimensional ◽  
Water Molecules ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Approximate Composition ◽  
Oxygen Atoms

SummaryThe crystal structures of sjögrenite and pyroaurite, two stacking modifications of approximate composition Mg6Fe2(OH)16(CO3).4H2O, have been determined by X-ray diffraction using three-dimensional methods. Sjögrenite is hexagonal, with a 3·13, c 15·66 Å, space group P63/mmc , Z = ¼; pyroaurite is rhombohedral, with aH 3·13, cH 23·49 Å, space group R3̄m or R3m, Z = ⅜. Both structures are based on brucite-like layers, with magnesium and iron distributed among the octahedral positions. The cations appear to be largely disordered, although ordered regions may occur in some crystals. Between the brucite-like layers are the water molecules and carbonate groups. These are statistically arranged, with their oxygen atoms distributed among a larger number of possible sites.

scholarly journals Hydrogen-bonding patterns in 2,2-bis(4-methylphenyl)hexafluoropropane pyridinium and ethylenediammonium salt crystals

2020 ◽  
Vol 76 (5) ◽  
pp. 742-746 ◽  
Author(s):  
Haruki Sugiyama
Keyword(s):  
Hydrogen Bonding ◽  
Crystal Structures ◽  
Three Dimensional ◽  
Water Molecules ◽  
Space Group ◽  
One Dimensional ◽  
Salt Crystals ◽  
Bonding Patterns ◽  
Hydrogen Bonded

The crystal structures of two salt crystals of 2,2-bis(4-methylphenyl)hexafluoropropane (Bmphfp) with amines, namely, dipyridinium 4,4′-(1,1,1,3,3,3-hexafluoropropane-2,2-diyl)dibenzoate 4,4′-(1,1,1,3,3,3-hexafluoropropane-2,2-diyl)dibenzoic acid, 2C5H6N+·C17H8F6O4 2−·C17H10F6O4, (1), and a monohydrated ethylenediammonium salt ethane-1,2-diaminium 4,4′-(1,1,1,3,3,3-hexafluoropropane-2,2-diyl)dibenzoate monohydrate, C2H10N2 2+·C17H8F6O4 2−·H2O, (2), are reported. Compounds 1 and 2 crystallize, respectively, in space group P21/c with Z′ = 2 and in space group Pbca with Z′ = 1. The crystals of compound 1 contain neutral and anionic Bmphfp molecules, and form a one-dimensional hydrogen-bonded chain motif. The crystals of compound 2 contain anionic Bmphfp molecules, which form a complex three-dimensional hydrogen-bonded network with the ethylenediamine and water molecules.

Sign in / Sign up

Export Citation Format

Share Document