ChemInform Abstract: Catalysis of Allylic Substitutions by Pd Complexes of Oxazolines Containing an Additional P, S, or Se Center. X-Ray Crystal Structures and Solution Structures of Chiral π-Allyl Palladium Complexes of Phosphinoaryloxazolines.

ChemInform ◽  
2010 ◽  
Vol 25 (30) ◽  
pp. no-no
Author(s):  
J. SPRINZ ◽  
M. KIEFER ◽  
G. HELMCHEN ◽  
M. REGGELIN ◽  
G. HUTTNER ◽  
...  
2005 ◽  
Vol 58 (5) ◽  
pp. 339 ◽  
Author(s):  
Ying Dong ◽  
Leonard F. Lindoy ◽  
Peter Turner

A selection of 1 : 1 (palladium/ligand) complexes of cyclam derivatives incorporating from one to three N-benzyl groups has been synthesized. Related 3 : 1 species of two symmetrically branched, tri-cyclam species incorporating 1,3,5-‘tribenzyl’ or phloroglucinol cores are also reported. The X-ray crystal structures of the palladium complexes of two isomeric forms of the N,N′-dibenzylated (single-ring) macrocycle have been determined. In each complex the palladium ion occupies the N4-plane of the respective macrocycles in a square planar arrangement, with each complex cation adopting a stable trans-III configuration.


1995 ◽  
Vol 48 (9) ◽  
pp. 1549 ◽  
Author(s):  
AA Watson ◽  
DA House ◽  
PJ Steel

The syntheses of 23 new chelating ligands are described. Most of these ligands are derived from the chiral pyrazole (1) which has been linked to a variety of heterocycles , namely pyridine, pyrimidine, pyridazine, isoxazole , benzimidazole, thiophen and furan. In certain cases the parent achiral analogues have also been prepared. Preliminary studies of the coordination chemistry of these ligands with selected transition metals have been carried out. The X-ray crystal structures of palladium complexes of isoxazole- and thiophen-containing ligands have also been determined.


Author(s):  
A. Zangvil ◽  
L.J. Gauckler ◽  
G. Schneider ◽  
M. Rühle

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.


1999 ◽  
Vol 82 (08) ◽  
pp. 271-276 ◽  
Author(s):  
Glen Spraggon ◽  
Stephen Everse ◽  
Russell Doolittle

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


2019 ◽  
Author(s):  
Yunyang Zhang ◽  
Janice Mui ◽  
Thimali Arumaperuma ◽  
James P. Lingford ◽  
ETHAN GODDARD-BORGER ◽  
...  

<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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