Cone angles for amine ligands. X-ray crystal structures and equilibrium measurements for ammonia, ethylamine, diethylamine, and triethylamine complexes with the [bis(dimethylphosphino)ethane]methylpalladium(II) cation

1991 ◽  
Vol 113 (7) ◽  
pp. 2520-2527 ◽  
Author(s):  
Allen L. Seligson ◽  
William C. Trogler
Keyword(s):  
Crystal Structures ◽  
X Ray ◽  
Amine Ligands

scholarly journals Neutral and Cationic Rhodium(III) Complexes with Tridentate Bis(benzimidazole)amine Ligands

1999 ◽  
Vol 23 (11) ◽  
pp. 642-643
Author(s):  
Monika Moszner ◽  
Ewa Kwaskowska-Chęć ◽  
Stanisław Wołowiec ◽  
Lucjan B. Jerzykiewicz ◽  
Józef J. Ziółkowski
Keyword(s):  
Ir Spectroscopy ◽  
Crystal Structures ◽  
Elemental Analysis ◽  
X Ray ◽  
Amine Ligands

The X-ray crystal structures of bis(benzimidazol-2-ylmethyl)methylamine (L) and N,N-bis(1-methylbenzimidazol-2-ylmethyl)methylamine (Me2L) are described; mono- and bis-ligand rhodium(III) complexes of L and Me2L are prepared and characterized by elemental analysis, conductometric measurements, NMR and IR spectroscopy.

Adducts of trimethylgallium and perdeuteriotrimethylgallium with amine ligands and some dimethylgallium organyl pnictides (N, P, As). X-ray crystal structures of [Me3Ga·NH(C6H11)2] and [Me3Ga·HMe]

Polyhedron ◽  
1990 ◽  
Vol 9 (2-3) ◽  
pp. 343-351 ◽  
Author(s):  
Donald C. Bradley ◽  
Helen M. Dawes ◽  
Michael B. Hursthouse ◽  
Lesley M. Smith ◽  
Mark Thornton-Pett
Keyword(s):  
Crystal Structures ◽  
X Ray ◽  
Amine Ligands

Transmission electron microscope studies in special ceramics

1978 ◽  
Vol 36 (1) ◽  
pp. 268-269
Author(s):  
A. Zangvil ◽  
L.J. Gauckler ◽  
G. Schneider ◽  
M. Rühle
Keyword(s):  
Phase Diagrams ◽  
Crystal Structures ◽  
Thin Foil ◽  
Limited Extent ◽  
Complex Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Electron Microscopes ◽  
Lattice Resolution

The use of high temperature special ceramics which are usually complex materials based on oxides, nitrides, carbides and borides of silicon and aluminum, is critically dependent on their thermomechanical and other physical properties. The investigations of the phase diagrams, crystal structures and microstructural features are essential for better understanding of the macro-properties. Phase diagrams and crystal structures have been studied mainly by X-ray diffraction (XRD). Transmission electron microscopy (TEM) has contributed to this field to a very limited extent; it has been used more extensively in the study of microstructure, phase transformations and lattice defects. Often only TEM can give solutions to numerous problems in the above fields, since the various phases exist in extremely fine grains and subgrain structures; single crystals of appreciable size are often not available. Examples with some of our experimental results from two multicomponent systems are presented here. The standard ion thinning technique was used for the preparation of thin foil samples, which were then investigated with JEOL 200A and Siemens ELMISKOP 102 (for the lattice resolution work) electron microscopes.

Crystal Structures of Fragments D and Double-D from Fibrinogen and Fibrin

1999 ◽  
Vol 82 (08) ◽  
pp. 271-276 ◽  
Author(s):  
Glen Spraggon ◽  
Stephen Everse ◽  
Russell Doolittle
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Crystal Structures ◽  
Structure And Function ◽  
X Ray ◽  
Long Period ◽  
And Function

IntroductionAfter a long period of anticipation,1 the last two years have witnessed the first high-resolution x-ray structures of fragments from fibrinogen and fibrin.2-7 The results confirmed many aspects of fibrinogen structure and function that had previously been inferred from electron microscopy and biochemistry and revealed some unexpected features. Several matters have remained stubbornly unsettled, however, and much more work remains to be done. Here, we review several of the most significant findings that have accompanied the new x-ray structures and discuss some of the problems of the fibrinogen-fibrin conversion that remain unresolved. * Abbreviations: GPR—Gly-Pro-Arg-derivatives; GPRPam—Gly-Pro-Arg-Pro-amide; GHRPam—Gly-His-Arg-Pro-amide

Synthesis of Sulfoquinovose and Sulfoquinovosyl Diacylglycerides, and a Fluorogenic Substrate for Sulfoquinovosidases

2019 ◽  
Author(s):  
Yunyang Zhang ◽  
Janice Mui ◽  
Thimali Arumaperuma ◽  
James P. Lingford ◽  
ETHAN GODDARD-BORGER ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Fluorogenic Substrate ◽  
Potassium Salts ◽  
X Ray ◽  
Sulfoquinovosyl Diacylglycerol ◽  
Sodium And Potassium

<p>The sulfolipid sulfoquinovosyl diacylglycerol (SQDG) and its headgroup, the sulfosugar sulfoquinovose (SQ), are estimated to harbour up to half of all organosulfur in the biosphere. SQ is liberated from SQDG and related glycosides by the action of sulfoquinovosidases (SQases). We report a 10-step synthesis of SQDG that we apply to the preparation of saturated and unsaturated lipoforms. We also report an expeditious synthesis of SQ and (<sup>13</sup>C<sub>6</sub>)SQ, and X-ray crystal structures of sodium and potassium salts of SQ. Finally, we report the synthesis of a fluorogenic SQase substrate, methylumbelliferyl a-D-sulfoquinovoside, and examination of its cleavage kinetics by two recombinant SQases.</p>

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