Synthesis, Characterization and X-Ray Crystal Structure of {H2B(Me2C3N2H)2}MoIVO(S2PPrI2)

1994 ◽  
Vol 47 (3) ◽  
pp. 471 ◽  
Author(s):  
LJ Laughlin ◽  
JM Gulbis ◽  
ERT Tiekink ◽  
CG Young
Keyword(s):  
Crystal Structure ◽  
Mass Spectrometric ◽  
Fourier Methods ◽  
Space Group ◽  
X Ray ◽  
R Value

Reaction of MoO (S2PPri2)2 and K{H2B(Me2C3N2H)2} in refluxing toluene produces green, diamagnetic, air-stable {H2B(Me2C3N2H)2}MoIVO(S2Ppri2)(1), which has been characterized by analytical, mass spectrometric, infrared and n.m.r. spectroscopic, and X-ray crystallographic techniques. Crystals of (1) are triclinic and belong to space group Pī , with a 10.289(1), b 13.601(2), c 8.737(1) Ǻ, α 94.31(1), β 107.71(1), γ 79.56(1)°, V 1145.2 Ǻ3 and Z 2. The structure was solved by Patterson and Fourier methods and refined by using 3631 reflections to a final R value of 0.024 ( Rw 0.041). The five-coordinate square pyramidal complex is composed of apical terminal oxo [Mo-O(1) 1.658(2)Ǻ] and bidentate H2B(Me2C3N2H)2- and S2PPri2- ligands coordinated to molybdenum. Ferrocenium oxidation of (1) produces the mononuclear molybdenum(V) complex [{H2B(Me2C3N2H)2}MoVO(S2Ppri2)]+ ( e.p.r .: g 1.964, a(95,97Mo) 41.7×10-4cm-1, a(31P) 30.1×10-4 cm-1).

Über die Kristallstruktur von KSc2 F7 / The Crystal Structure of KSc2 F7

1985 ◽  
Vol 40 (6) ◽  
pp. 726-729 ◽  
Author(s):  
Klaus Güde ◽  
Christoph Hebecker
Keyword(s):  
Crystal Structure ◽  
Single Crystals ◽  
Unit Cell ◽  
Space Group ◽  
X Ray ◽  
Monoclinic Unit Cell ◽  
R Value ◽  
Ray Methods

Abstract Single crystals of KSc2F7 have been prepared from a mixture of KF and ScF3 . The samples were investigated by X-ray methods. KSc2F7 crystallizes orthorhombically with a = 10.643(2), b = 6.540(1), c = 4.030(1) Å. These data indicate a close crystallographic connection to the monoclinic unit cell of KIn2F7 [1], But in contrast to KIn2F7 , KSc2 F7 crystallizes in space group No. 65. Cmmm - D192h. The R-value for 341 observed independent reflections is 0.060.

Synthese und Kristallstruktur von l,13-Bis(8-chinolyl)- 1,4,7,10,13-pentaoxatridecan-diquecksilber(I)-diperchlorat

1991 ◽  
Vol 46 (1) ◽  
pp. 1-4 ◽  
Author(s):  
Klaus Brodersen ◽  
Jörg Zimmerhackl
Keyword(s):  
Crystal Structure ◽  
Aqueous Solution ◽  
X Ray Diffraction ◽  
Triclinic Space Group ◽  
Space Group ◽  
X Ray ◽  
R Value ◽  
Torsional Angles ◽  
L 13 ◽  
Oxygen Atoms

1,13-Bis(8-quinolyl)-1,4,7,10,13-pentaoxatridecane-dimercury(I)-diperchlorate is formed by the reaction of 1,13-bis(8-quinolyl)-1,4,7,10,13-pentaoxatridecane in ethanol with an aqueous solution of dimercury(I)-diperchlorate.It crystallizes in the triclinic space group P Ī with a = 1020.6(2), b = 1200.6(8), c = 1441.1(6) pm , α = 69.60(5)°, β = 83.04(13)°, y = 66.53(4)° and Z = 2. The crystal structure was determined by X -ray diffraction and refined to an R-value o f 0.079. The Hg22+ -ion is coordinated to both nitrogen atoms and four oxygen atoms of one molecule of the ligand. By changing four C - O torsional angles from trans to gauche, the ligand adopts a helical, chiral configuration around the Hg22+-ion. The CIO4--ions are not coordinated to the Hg22+-ion.

Kristall- und Molekülstruktur von 5.10-Dihydro-5.10-diniethylphenaziniiimtniodid und 5.10-Dihydro-5.10-diethylphenaziniumtriiodid / Molecular and Crystal Structure of 5,10-Dihydro-5.10-dimethylphenaziniumtriiodide and 5.10-Dihydro-5.10-diethylphenazinium triiodide

1978 ◽  
Vol 33 (8) ◽  
pp. 838-842 ◽  
Author(s):  
H. J. Keller ◽  
W. Moroni ◽  
D. Nöthe ◽  
M. Scherz ◽  
J. Weiss
Keyword(s):  
Crystal Structure ◽  
Radical Cations ◽  
Unit Cell ◽  
Lattice Parameters ◽  
Molecular And Crystal Structure ◽  
Reaction Conditions ◽  
Space Group ◽  
X Ray ◽  
R Value

Oxidation of 5,10-dihydro-5,10-dimethylphenazine and 5,10-dihydro-5,10-diethyl-phenazine under different reaction conditions leads to several iodine containing solids. The preparation and X-ray structure of two of them, 5,10-dihydro-5,10-dimethyl-phcnaziniumtriiodide (3) and 5,10-dihydro-5,10-diethylphenaziniumtriiodido (4) are reported here.Compound 3 crystallizes in space group P21/n with lattice parameters a = 8.552(6) Å, b= 16.953(2) Å, c- 12.157(9) Å and β= 103.46(2)° with four formula units in the unit cell. The structure was refined to an R-value of 0.046 using 2387 independent reflections. The lattice constains distinct, slightly distorted triiodide ions and bent 5,10-dihydro-5,10-dimethylphenazinium radical cations. Compound 4 crystallizes in the same space group P21/n with lattice parameters a = 8.531(6) Å, b = 8.332(21) Å, c = 13.320(15) Å and β= 94.44(19)° with two formula units in the unit cell. The structure was refined to an R-value of 0.076 using 1195 independent reflections. The lattice contains strictly linear symmetrical triiodide ions and planar centrosymmetrical 5,10-dihydro-5,10-diethyl- phenazinium radical cations.

Synthese und Kristallstruktur von [Hg2(p-SC6H4NO2)]NO3 / Synthesis and Crystal Structure of [Hg2(p-SC6H4NO2)]NO3

1990 ◽  
Vol 45 (8) ◽  
pp. 1193-1196 ◽  
Author(s):  
Klaus Brodersen ◽  
Axel Knörr
Keyword(s):  
Crystal Structure ◽  
Chain Structure ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Synthesis And Crystal Structure ◽  
Space Group ◽  
X Ray ◽  
Nitrate Ions ◽  
R Value ◽  
A Chain

[Hg2(p-SC6H4NO2)]NO3 is formed by the reaction of p-nitrothiophenol with dimercury(I)-dinitrate in methanol. It crystallizes in the monoclinic space group P21/n with a = 1175.5(9) pm, b = 1079.8(8) pm, c = 876.2(8) pm, β = 110.74(4)° and Z = 4. The crystal structure has been determined by X-ray diffraction and refined to an R-value of 0.052. The results show that the compound exists as a chain structure of [—®S(C6H4NO2)— Hg— Hg—]n with nitrate ions connecting the chains.

Structural Aspects of V2( µ;-S2)2(S2CNR2)4 Complexes: the X-Ray Crystal Structure of V2( µ;-S2)2(S2CNEt2)4.2CHBr3

1992 ◽  
Vol 45 (5) ◽  
pp. 897 ◽  
Author(s):  
ERT Tiekink ◽  
XF Yan ◽  
CG Young
Keyword(s):  
Crystal Structure ◽  
Vanadium Atom ◽  
Single Bond ◽  
Dimeric Complex ◽  
Fourier Methods ◽  
Space Group ◽  
X Ray ◽  
Metal Metal ◽  
Structural Aspects

Brown V2(p-S2)2(S2CNEt2)4 is produced upon reaction of [vs4]3- with (Et2NCS2)2, in a synthesis similar to that described for V2( �-S2)2(S2CNBui2)4 ( Halbert , T. R., Hutchings, L. L., Rhodes, R., and Stiefel , E. I., J. Am. Chem. Soc., 1986, 108, 6437). Crystals of V2( �;-S2)2(S2CNEt2)4.2CHBr3 are orthorhombic and belong to space group Pbca , with a 10.909(2), b 20.492(2), c 20.471(2) � , V 4576.2 �3, and Z 4 dimers . The structure was solved by Patterson and Fourier methods and refined by using 1189 reflections to final R 0.061 ( Rw 0.059). The vanadium(IV) atoms in the dimeric complex are bridged by two �-k2S,S′: k2S,S′-S22- ligands [S(1)-S(2) 2.00(1) �] and a metal-metal single bond [V-V 2.900(6) �]. Each vanadium atom is further coordinated by two bidentate dithiocarbamate ligands whose arrangement defines a meso isomer with Λ and Δ configurations at the vanadium centres. This Λ Δ diastereomer differs from the Λ Λ -ΔΔ racemate structurally characterized in the case of V2(�-S2)2(S2CNBui2)4 but is the same as that found for the molybdenum(v) dication in [Mo2( �S2)2(S2CNEt2)4] (BF4)2.2CHBr3 ( Kocaba, T., Young, C. G., and Tiekink , E. R. T., Inorg. Chim. Acta, 1990, 174, 143).

Crystal Structure of Tetraethylammonium Bromopentacarbonyltungstate(0)

1995 ◽  
Vol 48 (5) ◽  
pp. 1045 ◽  
Author(s):  
T Whyte ◽  
GA Williams
Keyword(s):  
Crystal Structure ◽  
Single Crystal ◽  
Least Squares ◽  
X Ray Diffraction ◽  
Full Matrix ◽  
Space Group ◽  
X Ray ◽  
Bond Lengths ◽  
R Value

The crystal structure of tetraethylammonium bromopentacarbonyltungstate (0), [NEt4] [W(CO)5Br], has been determined by single-crystal X-ray diffraction methods at 22�1°C. Crystals are tetragonal, space group P4/n, with a 9.206(2), c 10.484(2) Ǻ, and Z 2. Full-matrix least-squares refinement gave a final R value of 0.034 for 820 independent reflections. The [W(CO)5Br]- anion possesses exact C4v symmetry, with bond lengths W-Br 2.736(1), W-COtrans 1.93(1) and W-COcis 2.034(6) Ǻ.

Nitridomolybdenum Complexes of Tris(3,5-dimethylpyrazol-1-yl)Hydroborate and the X-Ray Crystal-Structure of {HB(3,5-Me2C3N2H)3)MoN(N3)2

1990 ◽  
Vol 43 (8) ◽  
pp. 1347 ◽  
Author(s):  
CG Young ◽  
F Janos ◽  
MA Bruck ◽  
PA Wexler ◽  
JH Enemark
Keyword(s):  
Crystal Structure ◽  
Mass Spectrometry ◽  
Least Squares ◽  
Elemental Analysis ◽  
Bond Distance ◽  
Octahedral Complex ◽  
Fourier Methods ◽  
X Ray ◽  
Distorted Octahedral ◽  
R Value

The reaction of (NEt4)2[MoNCl5] and K{HB(Me2pz)3}[HB(Me2pz)3- = tris (3,5- dimethylpyrazol-1-yl) hydroborate anion] produces both purple, diamagnetic {HB(Me2pz)3}MoNCl2 (1) and yellow, paramagnetic Net4 [{HB(Me2pz)3}MoNCl2] (2) (e.s.r.: {g} 1.961, {a}(95Mo) 57×10-4 cm-1), which have been separately isolated under different conditions. In contrast, the reaction of [ MoN (N3)4]- with Na{HB(Me2pz)3} results in the exclusive formation of red {HB(Me2pz)3} MoN (N3)2 (3). Crystals of (3) are monoclinic and belong to space group P21/n with a 16.440(2), b 8.787(2), c 16.754(2) Ǻ,β 112.47(1)°, V 2236.4 Ǻ3, and Z 4. The structure was solved by Patterson and Fourier methods, followed by least-squares refinement, using 3208 reflections, to a conventional R value of 0.032 ( Rw 0.047). In the distorted octahedral complex the molybdenum(VI) atom is coordinated by a facial HB(Me2pz)3- ligand , a terminal nitrido ligand with a Mo-N bond distance of 1.646(4)Ǻ, and two azide ligands. All complexes have been characterized by elemental analysis, infrared, 1H n.m.r. or e.s.r. spectroscopy, and mass spectrometry. Improved syntheses for the starting materials (NEt4)2 [MoNCl5] and (NEt4)2 [MoNCl4] are also reported.

Notizen: Die Kristallstruktur von KLiTe / The Crystal Structure of KLiTe

1993 ◽  
Vol 48 (12) ◽  
pp. 1835-1836 ◽  
Author(s):  
Horst Sabrowsky ◽  
Rolf-Dieter Hitzbleck ◽  
Petra Vogt
Keyword(s):  
Crystal Structure ◽  
Single Crystals ◽  
X Ray Diffraction ◽  
Fourier Methods ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters

The crystal structure of KLiTe described earlier as a dark grey powder compound has been determined by X-ray diffraction of single crystals. Very hygroscopic KLiTe crystallizes in the tetragonal space group P4/nmm (Z = 2) with the cell parameters a = 483.0(1) and c = 770.4(2) pm. The structure was determined from 211 independent reflections by Patterson and Fourier methods (R = 0.013; wR = 0.013).

scholarly journals The crystal structure of 2-(4-bromophenyl)-4-(2-fluoroethyl)-5,6-dihydro-4H-1,3,4-oxadiazine hydrochloride, an octopaminergic insecticide/miticide

1995 ◽  
Vol 73 (6) ◽  
pp. 853-857 ◽  
Author(s):  
Mark A. Dekeyser ◽  
W. Ashley Harrison ◽  
Nicholas J. Taylor ◽  
Roger G.H. Downer
Keyword(s):  
Crystal Structure ◽  
Fourier Methods ◽  
Space Group ◽  
R Value

The crystal structure of 2-(4-bromophenyl)-4-(2-fluoroethyl)-5,6-dihydro-4H-1,3,4-oxadiazine hydrochloride, a new octopamine agonist, has been established by Patterson and Fourier methods and refined to a final R value of 0.0293 for 2123 absorption-corrected observed data. The crystals are monoclinic, a = 14.336(3), b = 12.649(3), c = 6.989(1) Å, β = 93.48(1)°, and the space group is P21/c. Its structural similarities with the crystal structure of the invertebrate neurotransmitter, octopamine, are described and support the hypothesis that the pesticidal properties of dihydrooxadiazines are, at least partially, due to perturbation of octopaminergic systems. Keywords: dihydrooxadiazine, octopamine agonist.

Kristallstruktur von Na4OBr2 / Crystal Structure of Na4OBr2

1990 ◽  
Vol 45 (2) ◽  
pp. 105-106 ◽  
Author(s):  
Karin Hippler ◽  
Stephan Sitta ◽  
Petra Vogt ◽  
Horst Sabrowsky
Keyword(s):  
Crystal Structure ◽  
Structure Type ◽  
X Ray Diffraction ◽  
Fourier Methods ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Group I

The colourless compound Na4OBr2 has been prepared and its crystal structure determined by X-ray diffraction. Very hygroscopic Na4OBr2 crystallizes in the tetragonal space group I 4/mmm (Z = 2) with the cell parameters a = 452.1(3) and c = 1490.8(1) pm. The structure was solved from 267 symmetry independent reflections by Patterson and Fourier methods (R = 0.028; wR = 0.029). Na4OBr2 crystallizes in the anti-K2NiF4-structure type and is isotypic to Na4OI2 and K4OBr2 which have been described earlier.

Sign in / Sign up

Export Citation Format

Share Document