Polymere Dimethyl-und Diphenylglyoximatokomplexe des Cobalts und Eisens mit 4.4′ -Bipyridin als Brückenligand. Die Kristallstruktur des Bis(dimethylglyoximato)4.4′-bipyridincobalt(II)*/ Polymeric Dimethyl-and Diphenylglyoximato Complexes of Cobalt and Iron with 4,4′-Bipyridine as a Bridging Ligand. The Crystal Structure of Bis(dimethylglyoximato)4,4′-bipyridine Cobalt(II)

1982 ◽  
Vol 37 (3) ◽  
pp. 272-275 ◽  
Author(s):  
Frank Kübel ◽  
Joachim Strähle

Polymeric bis(dimethyl- and diphenylglyoximato)-complexes of Fe(II) and Co(II) with 4,4′-bipyridine as a bridging ligand have been synthesized from the glyoximato metal complexes and 4,4′-bipyridine in ethanol. The Co(II) compounds are paramagnetic and surprisingly stable against oxidation. The iron complexes are weak electrical conductors with approximately 10-9 Ω-1cm-1 . Bis(dimethylglyoximato)-4,4′-bipyridine cobalt(II) crystallizes triclinic in the space group PT with Z=1. The crystal structure is built up by linear chains of alternating Co(II) glyoximato complexes and axial bonded 4,4′-bipyridine bridges. The compound is characterized by strong Co-N-bonds of 189 pm within the glyoximato moiety and weak bonds of 228 pm to the bipyridine ligand. The two heterocycles of the bipyridine are coplanar, therefore the local symmetry of the complex is D2h.

1981 ◽  
Vol 36 (4) ◽  
pp. 441-446 ◽  
Author(s):  
Frank Kübel ◽  
Joachim Strähle

Abstract Polymeric bis(dimethyl-and diphenylglyoximato)-complexes of Fe(II) and Co(II) with pyrazine as a bridging ligand have been synthesized. The Co(II) complexes are para-magnetic with μ = 1.83 B.M., and surprisingly stable against oxidation. Bis (dimethyl-glyoximato)pyrazine-cobalt (II) crystallizes monoclinic in the space group C2/m with Z = 2. The crystal structure shows linear chains of alternating Co atoms and pyrazine ligands. Perpendicular to the chain, the Co atoms are coordinated in a square planar arrangement by two dimethylglyoximato ligands (Co-N= 189 pm), the local symmetry being C2h-The long Co-pyrazine distance of 224 pm is in agreement with the fact that the compound is a 19 electron complex. The Co complexes do not have conducting properties. The Fe(II) complexes possess the same structure but with stronger bonds in the chain. They show very low conductivity of approximately 10-10 cm -1 Ω-1 . The Mössbauer spectra of the Fe-complexes are reported.


1989 ◽  
Vol 44 (5) ◽  
pp. 553-556 ◽  
Author(s):  
Th. Fetzer ◽  
A. Lentz ◽  
T. Debaerdemaeker

Single crystals of Cu(pz)Br2 and Cu(pz)Cl2 were grown by using gel methods with tetramethoxysilane as the gel-forming reagent. Thermal decomposition is interpreted. Crystal data for the bromo complex: monoclinic, space group C2/m with a = 1239.2(3) pm, b = 685.9(2) pm, c = 390.7(3) pm, β = 96,23(5)°. Crystal data for the chloro-complex: monoclinic, space group C2/m with a = 1197.1(3) pm, b = 684.9(3) pm, c = 370.1(3) pm, β = 95.96(5)°. Crystal structure analyses reveal that CuHal2 molecules are bonded by pyrazine to form linear chains. These chains are cross-linked by bridging halogen atoms.


1982 ◽  
Vol 37 (12) ◽  
pp. 1569-1572 ◽  
Author(s):  
Joachim Pickardt ◽  
Norbert Rautenberg

Crystals of the complex [Cu(NCO)2(C6Hi2N4)2] could be obtained by reaction of copper- (II)nitrate, hexamethylenetetramine, and KNCO in CHCI3 as a solvent. The crystals are triclinic, space group Cl, Z = 4, a = 1373.1(9), b = 2083.1(9), c = 642.6(3) pm, a = 91.05(4), β = 90.54(6), y = 107.39(6)°. The copper atom is bonded to two terminal cyanato groups via the nitrogen atoms, and to two liexamethylentetramine molecules. In the solid state the coordination of the copper atom is, however, tetragonal pyramidal, because there is an additional, rather long bond to one of the hexamethylenetetramine molecules of the neighbouring complex unit, resulting in the formation of chains


1988 ◽  
Vol 43 (4) ◽  
pp. 467-471 ◽  
Author(s):  
Ulf Thewalt ◽  
Konrad Holl

AbstractSlow reaction of TiCl4 with S4N4 in CH2Cl2/CCl4 produces a mixture of two crystalline dinuclear complexes of composition [TiCl4(S4N4)]2. Crystal data for the orange-yellow α-isomer: mono­clinic, space group P21/n with a = 11.608(3) Å. b = 8.304(3) Å, c = 10.938(5) Å, β = 101.06(4)° and Z = 2. Crystal data for the red-brown β-isomer: monoclinic, space group P21/c with a = 11.220(2) Å, b = 13.868(2) Å, c = 14.839(4) Å, β = 106.18(2)° and Z = 4. Crystal structure analyses reveal that the S4N4 molecules in the α-form act as 1,3-N,N′-bonded bridging ligands and in the β-form as N-bonded monodentate ligands.


2000 ◽  
Vol 55 (10) ◽  
pp. 988-991 ◽  
Author(s):  
Jens Klatyk ◽  
Rainer Niewa ◽  
Rüdiger Kniep

AbstractThe nitridom anganate(I) Ca{Li2[MnIN]2) (space group P4/mbm: a = 703.35(7), c = 383.19(6) pm; Z = 2) contains infinite linear chains 1∞=[MnIN2/22-] running along the [001] direction. The nitride species of the chains are further linked via three coordinated lithium to form planar 4.82-nets 2∞{Li2N24-} parallel (001). Ca2+ occupies the centers of the eight-membered rings of the planar nets. The 4.82-arrangement 2∞{Li2N24-} together with the stacking sequence ...AA... along [001] exhibit strong topological similarities with the anionic substructure 2∞[B2C22-] observed in the crystal structure of e.g. Ce[B2C2]


1981 ◽  
Vol 36 (10) ◽  
pp. 1225-1227 ◽  
Author(s):  
Joachim Pickardt

Abstract The reaction of aqueous solutions of cadmium iodide and hexamethylenetetramine yields crystals of an adduct 3CdI2 • 2CeH12N4 • 4H2O. The crystals are monoclinic, space group P 21/n, Z = 2, a = 811.5(2), b = 1049.2(4), c = 1849.5(6) pm, β = 97.73(2)°. The adduct is polymeric and may be regarded as built up from groups of two tetrahedrally and one octahedrally coordinated Cd(II) ions in which the tetrahedra and the octahedron are sharing common iodine atoms at the corners; neighbourirg Cd3 units are interlinked by hexamethylenetetramine molecules.


1985 ◽  
Vol 40 (10) ◽  
pp. 1237-1242 ◽  
Author(s):  
Herbert Bauer ◽  
George M. Sheldrick ◽  
Ulrich Nagel ◽  
Wolfgang Beck

The dinitrogen-tetrafluoroborato complex (Ph3P)2(Cl)(N2)(H)IrFBF3 reacts with 9-m ethylguanine in CH2Cl2 to give [(Ph3P)2(Cl)(H)Ir(9-methylguanine)]+BF4- (2). From a solution of 2 in methanol the complex (Ph3P)2(Cl)2(H)Ir(9-methylguanine) (3) is obtained. The reaction of [(Ph3P)2(Cl)(N2)(H)IrOSO2C4F9] with 9-methylguanine affords the com plexes [(Ph3P)2(Cl)(N2)(H)Ir(9-methylguanine)]+C4F9SO3- (5) and [(Ph3P)2(Cl)(H2O)(H)Ir(9-methylguanine)]+ C4F9SO3- (6). The coordination of the guanine derivative to the iridium atom in 2, 5, 6 is discussed on the basis of the infrared spectra. The crystal structure of 3 was determined. 9-Methylguanine is coordinated via N (7). Intermolecular hydrogen bonding between the chloro-ligand and HN (1) of guanine leads to linear chains in the crystal.


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