Powder X-ray data for adenosine C10H13N5O4

2000 ◽  
Vol 15 (2) ◽  
pp. 112-115 ◽  
Author(s):  
Ruggero Caminiti ◽  
Giancarlo Ortaggi ◽  
Raffaele Antonio Mazzei ◽  
Paolo Ballirano ◽  
Rita Rizzi
Keyword(s):  
Diffraction Data ◽  
Rietveld Analysis ◽  
Monoclinic Space Group ◽  
Angular Range ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Better Than

New powder X-ray diffraction data of adenosine C10H13N5O4 were reported: cell parameters are a=4.8386(4) Å, b=10.2919(4) Å, c=11.8555(4) Å, β=99.298(5)°, volume 582.63(4)Å for the monoclinic space group P21. The strongest lines are: 7.723 (100), 5.085 (50), 5.851 (45), 4.710 (11), 3.881 (10), 3.899 (9), 3.292 (9), and 3.261 (9). Reported intensities are validated by Rietveld analysis. The data consist of measured positions and intensities and cover an angular range up to 75° 2θ and are significantly better than PDF 35-1977. Experimental, calculated, and difference patterns are also reported.

Improved powder X-ray data for Cancrinites III: Davyne

1997 ◽  
Vol 12 (2) ◽  
pp. 99-102 ◽  
Author(s):  
Paolo Ballirano ◽  
Adriana Maras ◽  
Peter R. Buseck ◽  
Ann M. Yates
Keyword(s):  
Diffraction Data ◽  
Crystal Chemical ◽  
Angular Range ◽  
X Ray Diffraction ◽  
Hexagonal Cell ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters

New powder X-ray diffraction data of davyne, a member of the cancrinite group of minerals, were collected using a rotating anode diffractometer: the hexagonal cell parameters are a=12.6711(3) Å, c=5.3278(2) Å, volume 740.82(4) Å3 (space group P63). The strongest lines are: 3.658(100), 4.790(73), 3.272(70), 2.112(48), 2.438(22), 2.663(19), 1.781(19), and 4.147(17). The new data provide quantitative intensities improved precision in d-spacings and cover an increased 2θ angular range with respect to PDF 20-379. Measured intensities and a simulated pattern are reported together with crystal-chemical considerations.

Powder X-ray data for melatonin C13H16N2O2

2000 ◽  
Vol 15 (2) ◽  
pp. 108-111 ◽  
Author(s):  
Ruggero Caminiti ◽  
Giancarlo Ortaggi ◽  
Raffaele Antonio Mazzei ◽  
Paolo Ballirano ◽  
Rita Rizzi
Keyword(s):  
Diffraction Data ◽  
Cell Parameter ◽  
Rietveld Analysis ◽  
Angular Range ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Powder Diffractometer ◽  
Monoclinic Cell

Powder X-ray diffraction data of melatonin C13H16N2O2 were collected on a conventional X-ray powder diffractometer: the monoclinic cell parameter are a=7.7416(8) Å, b=9.2897(9) Å, c=17.1444(16) Å, β=96.756(9)°, volume 1224.4(3) Å3 (space group P21/c). The strongest lines are (d (Å), I/I0) 8.161 (100), 5.411 Å (46), 3.412 Å (34), 4.668 Å (33), 4.645 Å (25), 3.554 Å (22), 3.668 Å (16), and 4.483 Å (14). Reported intensities are validated by Rietveld analysis. The data consist of measured positions and intensities and cover an angular range up to 60° 2θ: experimental, calculated, and difference patterns are also reported.

Powder Diffraction Data for Trans-Bis (Dimethylphenylphosphine) Bis (Pyrazole) Platinum, [Pt(C3H4N2)2{P(CH3)2(C6H5)}2] and Trans-(Tricyclohexylphosphino)-(Triethylphosphino) Platinum(II) Chloride, PtCl2P2C24H48

1986 ◽  
Vol 1 (2) ◽  
pp. 33-34 ◽  
Author(s):  
D. F. Mullica ◽  
E. L. Sappenfield
Keyword(s):  
Powder Diffraction ◽  
Diffraction Data ◽  
Monoclinic Space Group ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Figures Of Merit

AbstractThe indexed X-ray diffraction powder data of trans-bis(dimethylphenylphosphine)bis(pyrazole)platinum, {Pt(C3H4N2)2[P(CH3)2(C6H5)]2, PTPP} and trans-(tricyclohexylphosphino) (triethylphosphino) platinum(II) chloride, (PtCl2P2C24H48, PTHE) are reported. PTPP crystallizes in the monoclinic space group C2/c and PTHE crystallizes in the orthorhombic space group Pcab. The refined cell parameters were determined by employing a Siemens Debye-Scherrer camera (Fe radiation, λmean = 1.93736 Å). The cell constants are a = 21.516(5), b = 6.287(1), c = 17.929(4)Å, β = 102.51(1)°, V = 2367.7Å3 Dx=1.70Mg m−3, Dm = 1.70Mg m−3 for PTPP and a = 12.271(1), b = 19.375(1), c = 23.864(3)Å, V = 5673.4Å3, Dx = 1.553Mg m−3 for PTHE. The quantitative figures of merit (FN) are F23 = 47(0.010,51) [F20 = 60(0.009,35)] for PTPP and F30 = 12(0.008,324) [F20 = 27(0.017,105)] for PTHE. The JCPD S Diffraction File No. for PTPP is 37-1999 and for PTHE is 37-2000.

Improved powder X-ray data for the cement phase Ca12Al14O32F2 (C11A7f)

2000 ◽  
Vol 15 (1) ◽  
pp. 56-61 ◽  
Author(s):  
Umberto Costa ◽  
Paolo Ballirano
Keyword(s):  
Diffraction Data ◽  
Cell Parameter ◽  
Rietveld Analysis ◽  
Crystal Chemical ◽  
Angular Range ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Powder Diffractometer

New powder X-ray diffraction data of Ca12Al14O32F2 (C11A7f), a cementitious compound, were collected on a conventional X-ray powder diffractometer; the cubic cell parameter is a=11.96269(6) Å, volume 1711.93(2) Å3 (space group I-43d (No. 220)). The strongest lines are 4.887(100), 2.676(95), 2.992(46), 2.443(46), 2.185(37), 3.198(32), 1.599(26), and 1.941(25). Reported intensities are validated by Rietveld analysis. The new data consist of measured intensities and cover a wider 2θ angular range with respect to the calculated PDF 25-394 and the indexed PDF 36-678: experimental, calculated, and difference patterns are reported together with crystal-chemical considerations.

Anionische Komplexe [Mo2(O2CPh)4X2]2⊖ mit X = N3, Cl, Br. Die Kristallstruktur von (PPh4)2[Mo2(O2CPh)4Cl2] · 2CH2Cl2 / Anionic Complexes [Mo2(O2C-Ph)4X2]2⊖ with X = N3, Cl, Br. The Crystal Structure of (PPh4)2[Mo2(O2C-Ph)4Cl2] · 2CH2Cl2

1985 ◽  
Vol 40 (1) ◽  
pp. 13-18 ◽  
Author(s):  
Kay Jansen ◽  
Kurt Dehnicke ◽  
Dieter Fenske
Keyword(s):  
Crystal Structure ◽  
Ir Spectra ◽  
Diffraction Data ◽  
Unit Cell ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
Lattice Constants ◽  
Anionic Complexes

The syntheses and IR spectra of the complexes [Mo2(O2C-Ph)4X2]2⊖ with X = N3, CI, Br and the counter ion PPh4⊕ are reported. The azido and the bromo complexes are obtained from a solution of [Mo2(O2CPh)4] with PPh4N3 in pyridine or by reaction with PPh4Br in CH2Br2, respectively. When (PPh4)2[Mo2(O2CPh)4(N3)2] is dissolved in CH2Cl2, nitrogen is evolved and the complex with X = CI is obtained. The crystal structure of (PPh4)2[Mo2(O2CPh)4Cl2] · 2CH2Cl2 was determined from X-ray diffraction data (5676 observed independent reflexions, R = 0.042). It crystallizes in the monoclinic space group P21/n with four formula units per unit cell; the lattice constants are a = 1549, b = 1400, c = 1648 pm, β = 94.6°. The centrosymmetric [Mo2(O2CPh)4Cl2]2⊖ ion has a rather short Mo-Mo bond of 213 pm, whereas the MoCl bonds are very long (288 pm)

scholarly journals Cloning, purification, crystallization and preliminary X-ray diffraction of the OleC protein fromStenotrophomonas maltophiliainvolved in head-to-head hydrocarbon biosynthesis

2010 ◽  
Vol 66 (9) ◽  
pp. 1108-1110 ◽  
Author(s):  
Janice A. Frias ◽  
Brandon R. Goblirsch ◽  
Lawrence P. Wackett ◽  
Carrie M. Wilmot
Keyword(s):  
Diffraction Data ◽  
Unit Cell ◽  
Biosynthetic Enzyme ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Hydrocarbon Biosynthesis

OleC, a biosynthetic enzyme involved in microbial hydrocarbon biosynthesis, has been crystallized. Synchrotron X-ray diffraction data have been collected to 3.4 Å resolution. The crystals belonged to space groupP3121 orP3221, with unit-cell parametersa=b= 98.8,c= 141.0 Å.

On racemic and L-malates: a comparison of their crystal structures

2004 ◽  
Vol 219 (2) ◽  
Author(s):  
Michel Fleck ◽  
Ekkehart Tillmanns ◽  
Ladislav Bohatý ◽  
Peter Held
Keyword(s):  
Single Crystal ◽  
Crystal Structures ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Monoclinic Space Group ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
Powder Diffraction File ◽  
Space Group ◽  
X Ray

AbstractThe crystal structures of eight different L-malates have been determined and refined from single-crystal X-ray diffraction data. The compounds are the monoclinic (space groupIn addition, for all the compounds, powder diffraction data were collected, analysed and submitted to the powder diffraction file (PDF).

X-ray diffraction data of Ti2O2(C2O4)(OH)2·H2O

1994 ◽  
Vol 9 (3) ◽  
pp. 187-188 ◽  
Author(s):  
Hee-Lack Choi ◽  
Naoya Enomoto ◽  
Nobuo Ishizawa ◽  
Zenbe-e Nakagawa
Keyword(s):  
Powder Diffraction ◽  
Diffraction Data ◽  
Unit Cell ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Crystal System

X-ray powder diffraction data for Ti2O2(C2O4)(OH)2·H2O were obtained. The crystal system was determined to be orthorhombic with space group C2221. The unit cell parameters were refined to a = 1.0503(2) nm, b = 1.5509(3) nm, and c = 0.9700(1) nm.

scholarly journals Crystallization and preliminary X-ray diffraction studies of guanidinoacetate methyltransferase from rat liver

1999 ◽  
Vol 55 (11) ◽  
pp. 1928-1929 ◽  
Author(s):  
Junichi Komoto ◽  
Yafei Huang ◽  
Yongbo Hu ◽  
Yoshimi Takata ◽  
Kiyoshi Konishi ◽  
...  
Keyword(s):  
Rat Liver ◽  
Unit Cell ◽  
Monoclinic Space Group ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters

Guanidinoacetate methyltransferase is the enzyme which catalyzes the last step of creatine biosynthesis. The enzyme is found ubiquitously and in abundance in the livers of all vertebrates. Recombinant rat-liver guanidinoacetate methyltransferase has been crystallized with guanidinoacetate and S-adenosylhomocysteine. The crystals belong to the monoclinic space group P21, with unit-cell parameters a = 54.8, b = 162.5, c = 56.1 Å, β = 96.8 (1)° at 93 K, and typically diffract beyond 2.8 Å.

scholarly journals On the crystal structure of the ordered vacancy compound Cu3In5Te9

2019 ◽  
Vol 65 (4 Jul-Aug) ◽  
pp. 360 ◽  
Author(s):  
G. E. Delgado ◽  
C. Rincón ◽  
G. Marroquin
Keyword(s):  
Crystal Structure ◽  
Diffraction Data ◽  
Rietveld Method ◽  
Structural Models ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Unit Cell Parameters ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters

The crystal structure of the ordered vacancy compound (OVC) Cu3In5Te9 was analyzed using powder X-ray diffraction data. Several structural models were derived from the structure of the Cu-poor Cu-In-Se compound b-Cu0.39In1.2Se2 by permuting the cations in the available site positions. The refinement of the best model by the Rietveld method in the tetragonal space group P2c (Nº 112), with unit cell parameters a = 6.1852(2) Å, c = 12.3633(9) Å, V = 472.98(4) Å3, led to Rp = 7.1 %, Rwp = 8.5 %, Rexp = 6.4 %, S = 1.3 for 162 independent reflections. This model has the following Wyckoff site atomic distribution: Cu1 in 2e (0,0,0); In1 in 2f (½,½,0), In2 in 2d (0,½,¼); Cu2-In3 in 2b (½,0,¼); in 2a (0,0,¼); Te in 8n (x,y,z).

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