Synthesis, Characterization, and Reactions of the Cluster Complexes Containing the Tetrahedral Cluster Core MFeCoS (M = Mo, W) and a Functionally Substituted Cyclopentadienyl Ligand. The Single Crystal X-ray Structures of Two Double Clusters, [.eta.5-C5H4C(O)CH2CH2C(O)C5H4-.eta.5][M(CO)2Fe(CO)3Co(CO)3(.mu.3-S)]2 (M = Mo, W)

1995 ◽  
Vol 14 (1) ◽  
pp. 98-106 ◽  
Author(s):  
Li-Cheng Song ◽  
Jin-Yu Shen ◽  
Qing-Mei Hu ◽  
Xiao-Ying Huang
Keyword(s):  
Single Crystal ◽  
Cluster Core ◽  
Tetrahedral Cluster ◽  
Cluster Complexes ◽  
X Ray ◽  
Cyclopentadienyl Ligand

Synthesis and Crystal Structures of Dimethylsilylene-Bridged (Amidocyclopentadienyl)dichlorotitanium(IV) Complexes with Various Substituents on the Cyclopentadienyl Ligand

2001 ◽  
Vol 66 (4) ◽  
pp. 605-620 ◽  
Author(s):  
Jaroslav Zemánek ◽  
Petr Štěpnička ◽  
Karla Fejfarová ◽  
Róbert Gyepes ◽  
Ivana Císařová ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Solid State ◽  
Single Crystal ◽  
Spectral Methods ◽  
Nmr Spectra ◽  
Bulky Substituent ◽  
State Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cyclopentadienyl Ligand

(Amidocyclopentadienyl)dichlorotitanium(IV) complexes of the general formula [TiCl2{η5:η1(N)-C5(1-SiMe2Nt-Bu-2,3,4-Me3-5-R)}], where R = H (6b), Ph (6c), 4-fluorophenyl (6d) and 1-methylallyl (6e) were synthesized and characterized by spectral methods. Solid-state structure of [TiCl2{η5:η1(N)-C5Me4(SiMe2Nt-Bu)}] (6a) and 6d determined by single-crystal X-ray diffraction showed that variation of the ring substituent R has only a negligible effect on the molecular structure of the complexes. The NMR spectra indicate that motion of the bulky substituent R in compounds 6c, 6d and 6e is hindered below ca 50 °C.

Electron Microscopy of Shock Loaded Polycrystalline Beryllium

1974 ◽  
Vol 32 ◽  
pp. 506-507 ◽  
Author(s):  
J. M. Galbraith ◽  
L. E. Murr ◽  
A. L. Stevens
Keyword(s):  
Electron Microscopy ◽  
Wave Propagation ◽  
Structural Change ◽  
Single Crystal ◽  
Diffraction Pattern ◽  
Shock Loading ◽  
Slip Systems ◽  
Compression Tests ◽  
X Ray Diffraction ◽  
X Ray

Uniaxial compression tests and hydrostatic tests at pressures up to 27 kbars have been performed to determine operating slip systems in single crystal and polycrystal1ine beryllium. A recent study has been made of wave propagation in single crystal beryllium by shock loading to selectively activate various slip systems, and this has been followed by a study of wave propagation and spallation in textured, polycrystal1ine beryllium. An alteration in the X-ray diffraction pattern has been noted after shock loading, but this alteration has not yet been correlated with any structural change occurring during shock loading of polycrystal1ine beryllium.This study is being conducted in an effort to characterize the effects of shock loading on textured, polycrystal1ine beryllium. Samples were fabricated from a billet of Kawecki-Berylco hot pressed HP-10 beryllium.

Crystal structure of an inclusion complex between chiral monoaza-15-crown-5 and S(–)-1-phenyl-ethyl ammonium percholorate

2003 ◽  
Vol 218 (5) ◽  
Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Type

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group

Single Crystal Growth of High-Pressure Phases of Ice and Salt Hydrate Far Below the Original Melting Point by Mixing Alcohol: Crystal Structure Determination of Magnesium Chloride Heptahydrate

2020 ◽  
Author(s):  
Keishiro Yamashita ◽  
Kazuki Komatsu ◽  
Hiroyuki Kagi
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
Crystal Growth ◽  
Single Crystal ◽  
Room Temperature ◽  
Growth Technique ◽  
Salt Hydrate ◽  
X Ray

An crystal-growth technique for single crystal x-ray structure analysis of high-pressure forms of hydrogen-bonded crystals is proposed. We used alcohol mixture (methanol: ethanol = 4:1 in volumetric ratio), which is a widely used pressure transmitting medium, inhibiting the nucleation and growth of unwanted crystals. In this paper, two kinds of single crystals which have not been obtained using a conventional experimental technique were obtained using this technique: ice VI at 1.99 GPa and MgCl<sub>2</sub>·7H<sub>2</sub>O at 2.50 GPa at room temperature. Here we first report the crystal structure of MgCl2·7H2O. This technique simultaneously meets the requirement of hydrostaticity for high-pressure experiments and has feasibility for further in-situ measurements.

Tris(pyrazolyl)borate Copper Hydroxide Complexes Featuring Tunable Intramolecular H-bonding

2019 ◽  
Author(s):  
Evan Gardner ◽  
Caitlyn Cobb ◽  
Jeffery A. Bertke ◽  
Timothy H. Warren
Keyword(s):  
Single Crystal ◽  
Copper Hydroxide ◽  
X Ray ◽  
Modular Synthesis ◽  
Pendant Arm ◽  
Copper Center ◽  
Vibrational Studies

A modular synthesis provides access to a series of new tris(pyrazolyl)borate ligands <sup>XpyMe</sup>TpK that possess a single functionalized pendant pyridyl (py) or pyrimidyl (pyd) arm designed to engage in tunable intramolecular H-bonding to metal–bound functionalities. To illustrate such H-bonding interactions, a series of [<sup>XpyMe</sup>TpCu]<sub>2</sub>(𝜇–OH)<sub>2</sub>(<b>6a</b><b>–6e</b>) complexes were synthesized from the corresponding <sup>XpyMe</sup>TpCu–OAc (<b>5a–5e</b>) complexes. Single crystal X-ray structures of three new dinuclear [<sup>XpyMe</sup>TpCu]<sub>2</sub>(𝜇–OH)<sub>2</sub>complexes reveal H-bonding between the pendant heterocycle and bridging hydroxide ligands while the donor arm engages the copper center in an unusual monomeric <sup>DMAPMe</sup>TpCu–OH complex. Vibrational studies (IR) of each bridging hydroxide complex reveal reduced 𝜈<sub>OH </sub>frequencies that tracks with the H-bond accepting ability of the pendant arm.

Tris(pyrazolyl)borate Copper Hydroxide Complexes Featuring Tunable Intramolecular H-bonding

2019 ◽  
Author(s):  
Evan Gardner ◽  
Caitlyn Cobb ◽  
Jeffery A. Bertke ◽  
Timothy H. Warren
Keyword(s):  
Single Crystal ◽  
Copper Hydroxide ◽  
X Ray ◽  
Modular Synthesis ◽  
Pendant Arm ◽  
Copper Center ◽  
Vibrational Studies

A modular synthesis provides access to a series of new tris(pyrazolyl)borate ligands <sup>XpyMe</sup>TpK that possess a single functionalized pendant pyridyl (py) or pyrimidyl (pyd) arm designed to engage in tunable intramolecular H-bonding to metal–bound functionalities. To illustrate such H-bonding interactions, a series of [<sup>XpyMe</sup>TpCu]<sub>2</sub>(𝜇–OH)<sub>2</sub>(<b>6a</b><b>–6e</b>) complexes were synthesized from the corresponding <sup>XpyMe</sup>TpCu–OAc (<b>5a–5e</b>) complexes. Single crystal X-ray structures of three new dinuclear [<sup>XpyMe</sup>TpCu]<sub>2</sub>(𝜇–OH)<sub>2</sub>complexes reveal H-bonding between the pendant heterocycle and bridging hydroxide ligands while the donor arm engages the copper center in an unusual monomeric <sup>DMAPMe</sup>TpCu–OH complex. Vibrational studies (IR) of each bridging hydroxide complex reveal reduced 𝜈<sub>OH </sub>frequencies that tracks with the H-bond accepting ability of the pendant arm.

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