Synthesis, Crystal Structure, and Magnetic Property of Delithiated LixMnO2 (x < 0.1) Single Crystals: A Novel Disordered Rocksalt-Type Manganese Dioxide.

Some novel cobalt diphenylphosphine complexes were synthesized by reacting cobalt(II) chloride with (2-methoxyethyl)diphenylphosphine, (2-methoxyphenyl)diphenylphosphine, and 2-(1,1-dimethylpropyl)-6-(diphenylphosphino)pyridine. Single crystals suitable for X-ray diffraction studies were obtained for the first two complexes, and their crystal structure was determined. The novel compounds were then used in association with methylaluminoxane (MAO) for the polymerization of 1,3-butadiene, and their behavior was compared with that exhibited in the polymerization of the same monomer by the systems CoCl2(PnPrPh2)2/MAO and CoCl2(PPh3)2/MAO. Some significant differences were observed depending on the MAO/Co ratio used, and a plausible interpretation for such a different behavior is proposed.

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Zum Mineral Johillerit verwandte Oxovanadate RbCd4V3O12 und TlCd4V3O12 / Oxovanadates RbCd4V3O12 and TlCd4V3 O12 Related to the Mineral Johillerite

Zeitschrift für Naturforschung B ◽

10.1515/znb-1997-0520 ◽

1997 ◽

Vol 52 (5) ◽

pp. 663-668 ◽

Cited By ~ 4

Author(s):

B. Mertens ◽

Hk. Müller-Buschbaum

Keyword(s):

Crystal Structure ◽

Solid State ◽

Single Crystals ◽

Solid State Reactions ◽

Space Group ◽

Related Compounds

Abstract Single crystals of I RbCd4V3O12 and TlCd4V3O12 II have been prepared by solid state reactions in closed iron tubes. The compounds crystallize closely related to the Johillerite structure in the space group C62h- C2/c with I: a = 13.058(3); b - 13.528(3), c = 7 .0 6 0 (2 )Å , β = 114.88(2)°; II: a = 12.999(6), b = 13.527(7), c = 7.055(3) Å , β = 114.88(4)°, Z = 4. Special features are the loss of Cu2+ in order to gain an additional Cd2+ position. The crystal structure is discussed with respect to related compounds of the Johillerite type.

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Two lithium tricyanomethanide compounds: syntheses and single-crystal structure determination of LiK[C(CN)3]2 and Li[C(CN)3]·½ (H3C)2CO

Zeitschrift für Naturforschung B ◽

10.1515/znb-2014-0250 ◽

2015 ◽

Vol 70 (3) ◽

pp. 191-196 ◽

Cited By ~ 1

Author(s):

Olaf Reckeweg ◽

Francis J. DiSalvo

Keyword(s):

Crystal Structure ◽

Single Crystal ◽

Single Crystals ◽

Structure Determination ◽

Monoclinic Space Group ◽

Orthorhombic Space Group ◽

Space Group ◽

Cell Parameters ◽

New Compounds

AbstractThe new compounds LiK[C(CN)3]2 and Li[C(CN)3]·½ (H3C)2CO were synthesized and their crystal structures were determined. Li[C(CN)3]·½ (H3C)2CO crystallizes in the orthorhombic space group Ima2 (no. 46) with the cell parameters a=794.97(14), b=1165.1(2) and c=1485.4(3) pm, while LiK[C(CN)3]2 adopts the monoclinic space group P21/c (no. 14) with the cell parameters a=1265.7(2), b=1068.0(2) and c=778.36(12) pm and the angle β=95.775(7)°. Single crystals of K[C(CN)3] were also acquired, and the crystal structure was refined more precisely than before corroborating earlier results.

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Calcium Carbodiimide Compounds Revisited – Syntheses, Single Crystal Structure Determination and Vibrational Spectra of Ca11N6[CN2]2, Ca4N2[CN2] and Ca[CN2]

Zeitschrift für Naturforschung B ◽

10.1515/znb-2008-0509 ◽

2008 ◽

Vol 63 (5) ◽

pp. 530-536 ◽

Cited By ~ 8

Author(s):

Olaf Reckeweg ◽

Francis J. DiSalvo

Keyword(s):

Crystal Structure ◽

Raman Spectrum ◽

Single Crystal ◽

Single Crystals ◽

Vibrational Spectra ◽

Structure Determination ◽

X Ray ◽

Characteristic Features ◽

Reported Data ◽

Correct Data

Single crystals of Ca11N6[CN2]2 (dark red needles, tetragonal, P42/mnm (no. 136), a = 1456.22(5), and c = 361.86(2) pm, Z = 2), Ca4N2[CN2] (transparent yellow needles, orthorhombic, Pnma (no. 62), a = 1146.51(11), b = 358.33(4), and c = 1385.77(13) pm, Z = 4) and Ca[CN2] (transparent, colorless, triangular plates, rhombohedral, R3̅m (no. 166), a = 369.00(3), and c = 1477.5(3) pm, Z = 3) were obtained by the reaction of Na2[CN2], CaCl2 and Ca3N2 (if demanded by stoichiometry) in arc-welded Ta ampoules at temperatures between 1200 - 1400 K. Their crystal structures were re-determined by means of single crystal X-ray structure analyses. Additionally, the Raman spectra were recorded on these same single crystals, whereas the IR spectra were obtained with the KBr pellet technique. The title compounds exhibit characteristic features for carbodiimide units with D∞h symmetry (d(C-N) = 121.7 - 123.8 pm and ∡ (N-C-N) = 180°). The vibrational frequencies of these units are in the expected range (Ca11N6[CN2]2: νs = 1230, νs = 2008; δ = 673/645/624 cm−1; Ca4N2[CN2]: νs = 1230, νs = 1986; δ = 672/647 cm−1; Ca[CN2]: νs = 1274, νs = 2031, δ = 668 cm−1). The structural results are more precise than the previously reported data, and with the newly attained Raman spectrum of Ca11N6[CN2]2 we correct data reported earlier.

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Magnetic property and crystal structure of bis [N-(4-chlorophenyl) salicylideneaminato] oxovanadium (IV)

Chemical Physics Letters ◽

10.1016/j.cplett.2010.01.057 ◽

2010 ◽

Vol 488 (1-3) ◽

pp. 32-37 ◽

Cited By ~ 8

Author(s):

Naoki Matsuoka ◽

Hiroshi Kawamura ◽

Naoki Yoshioka

Keyword(s):

Crystal Structure ◽

Magnetic Property

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The crystal structure of arsenic telluroxide AsTe0.5O2

Zeitschrift für Kristallographie - Crystalline Materials ◽

10.1524/zkri.1993.205.part-1.27 ◽

1993 ◽

Vol 205 (1) ◽

Cited By ~ 2

Author(s):

A. C. Stergiou

Keyword(s):

Crystal Structure ◽

Least Squares ◽

Single Crystals ◽

Direct Methods ◽

Anomalous Dispersion ◽

Thermal Parameters ◽

Trigonal Prism ◽

Population Parameter ◽

Full Matrix

AbstractSingle crystals of AsTeSolution of the structure was essentialy effected by direct methods combined with successive Fourier syntheses. The positional and anisotropic thermal parameters were refined by full-matrix least-squares calculations. Absorption and anomalous dispersion corrections were applied to all atoms. The finalThe As atom is coordinated by six O atoms forming a right trigonal prism. The Te atom site is partially occupied by Te atoms with a population parameter 0.5 and surrounded by six O atoms also forming a right trigonal prism. The structure looks like that of NiAs. Each of the AsO

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A-Pr2S3, D-Ho2S3 und E-Yb2S3:Synthese und Einkristallstrukturuntersuchungen / A-Pr2S3, D-Ho2S3 and E-Yb2S3:Synthesis and Single Crystal Structure Investigations

Zeitschrift für Naturforschung B ◽

10.1515/znb-1996-0519 ◽

1996 ◽

Vol 51 (5) ◽

pp. 733-738 ◽

Cited By ~ 16

Author(s):

Thomas Schleid ◽

Falk Lissner

Keyword(s):

Crystal Structure ◽

Crystal Growth ◽

Single Crystals ◽

Alkali Halides ◽

Structural Investigations ◽

Coordination Numbers ◽

Trivalent Lanthanides ◽

Trivalent Cations ◽

Structure Investigations ◽

Type Orthorhombic

The oxidation of reduced chlorides (MCl2) or chloride-hydrides (MClHx) of the lanthanides with sulfur (700-850 °C, 7 d, sealed tantalum capsules or evacuated silica vessels) usually results in the formation of the sesquisulfides M2S3 as the main products. In the presence of appropriate fluxes (e.g., alkali halides), the products often are obtained as single crystals, and the flux decides which modification is favoured. Ternary halides of the trivalent lanthanides with the corresponding alkali metal can mostly be found as the second components. Crystal growth and structural investigations of thus produced single crystals of Pr2S3 (from PrClH0.67 + S + NaCl, 5:5:1, A type: orthorhombic, Pnma (No. 62), Z = 4, a = 748.22(5), b = 405.51(3), c = 1560.74(9) pm, R = 0.024, Rw = 0.020), Ho2S3, (from U - Ho2S3, + KI, 1:1, D type: monoclinic, P21/m (No. 12), Z = 6, a = 1746.15(9), b = 400.23(3), c = 1012.43(6) pm, β = 98.529(4)°, R = 0.041, Rw = 0.035), and Yb2S3 (from T-Yb2S3 + KI, 1:1, E type: trigonal, R3̄c (No. 167), Z = 6, a = 674.97(2), c = 1820.11(9) pm, R = 0.019, Rw = 0.018) are reported here. In accordance with the lanthanide contraction, the trivalent cations (M3+) exhibit sulfur coordination numbers of 7 and 8 in A -Pr2S3, 6 and 7 in D -Ho2S3, and 6 in E -Yb2S3 (corundum-type structure).

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