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1Author    Sigurd Elz, Martin Dräger, Hans-Joachim Sattler, Walter SchunackRequires cookie*
 Title    Synthese und Absolute Konfiguration von (+)-l-Amino-2-propanthiol-HCl Synthesis and Absolute Configuration of ( + )-l-Amino-2-propanethiol * HCl  
  Reference    Z. Naturforsch. 42b, 617—622 (1987); eingegangen am 22. August 1986 
  Published    1987 
  Keywords    Amino-2-propanethiol, Crystal Structure, Diastereomers, Impromidine, Thiazolidines 
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 TEI-XML for    default:Reihe_B/42/ZNB-1987-42b-0617.pdf 
 Identifier    ZNB-1987-42b-0617 
 Volume    42 
2Author    Henri Brunner, M. Arkus, N. Iem Etz, M. Anfred ZabelRequires cookie*
 Title    Optisch aktive Ubergangsmetall-Komplexe, 122 [1]. Synthese von Palladium(II)-Schiff-Base-Komplexen -intramolekulare Wechselwirkungen O ptically Active Transition M etal C om plexes, 122 [1], Synthesis of Palladium (II) Com plexes w ith Schiff B ase Ligands -Intram olecular Interactions  
 Abstract    Imines of salicylaldehyde and 2,6-diformyl-p-cresol have been used as ligands in palla­ d iu m ^) complexes. Enantiomerically pure ligands give enantiomerically pure complexes, racemic ligands give racemates and meso-forms. Differences between the respective isomers of the ligands within the complexes and between the diastereomers of the complexes were investigated. Crystal structure analyses established the trans configuration at the metal center. 
  Reference    Z. Naturforsch. 55b, 145—154 (2000); eingegangen am 25. Oktober 1999 
  Published    2000 
  Keywords    Schiff Bases, Palladium(II) Complexes, Diastereomers, Crystal Structure 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0145.pdf 
 Identifier    ZNB-2000-55b-0145 
 Volume    55 
3Author    V. Villa, F. Fischer3, J. ThiembRequires cookie*
 Abstract    o le k u la r e s V e rd rillu n g s v e rm ö g e n von K o h le n h y d ra t-D e riv a te n Helical Twisting Power of Carbohydrate Derivatives For the first time carbohydrate derivatives were systematically studied as doping material for a liquid crystalline phase. These compounds can exhibit a large twisting power. It may be controlled by the configurations of single chiral centers. Thus, a series of phenomena are realized in the cholesteric phase such as helix inversion, large or small temperature dependencies of the pitch, as well as broad blue phases. Durch Zugabe einer chiralen, löslichen Substanz zu einer nematischen Phase läßt sich die cholesterische Phase erzeugen [1], Neben neu synthetisierten Ver­ bindungen wurden auch zahlreiche Naturstoffe, vor­ nehmlich Isoprenoide eingesetzt. Kohlenhydratderi-vate wurden dagegen vermutlich aufgrund ihrer er­ heblichen Polarität bisher nicht in Betracht gezogen. Diese chemisch robusten und leicht zugänglichen Ver­ bindungen erscheinen ideal geeignet zu sein, da sich mit ihnen in einmaliger Weise alle stereochemischen Möglichkeiten realisieren lassen. Zur Überprüfung der Eignung von Kohlenhydrat-Derivaten als chirale Zusätze zu nematischen Phasen wurden 22 Mischungen untersucht. Als Wirtssubstanz diente jeweils 4-n-Butyloxy-phenyl-4'-n-hexyloxybenzoat (1, ZLI 1792). Als chirale Zusätze wurden gewählt (s. Tab. 1): 
  Reference    Z. Naturforsch. 43a, 1119—1125 (1988); eingegangen am 30. September 1988 
  Published    1988 
  Keywords    Helical twisting power, carbohydrates, induced cholesteric phase, diastereomers, liquid crystals 
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 TEI-XML for    default:Reihe_A/43/ZNA-1988-43a-1119.pdf 
 Identifier    ZNA-1988-43a-1119 
 Volume    43 
4Author    RolfW. Saalfrank3, Oliver Struck3, Karl Petersb, HansG. Eorg, Von SchneringbRequires cookie*
 Title    Synthese und Struktur diastereomerer, zweikerniger Kupferkomplexe [1] Synthesis and Structure of Diastereomerie Dinuelear C opper Complexes [1]  
 Abstract    Depolym erisation of a copper(II)/pyrrolidine-based 2D -polym er 2 by 4.4'-bipyridyl [molar ratio: 2 (C u L 2) : l (Bipy)] and recrystallisation o f the reaction product leads to two visually distinguishable crystal charges, composed of dark green octahedra m eso-4 and light green rod-shaped crystals racem-5. Separation of the conglom erate of the morphologically different crystals is accomplished by pick out. The structure of the dinuelear complex racem-5 has been established unambigously by X-ray structure analysis. EPR and susceptibility measure­ ments of mixtures of complex meso-4 and racem-S indicate that there is no interaction be­ tween the two copper(II) centres. 
  Reference    Z. Naturforsch. 49b, 1410—1414 (1994); eingegangen am 17. März 1994 
  Published    1994 
  Keywords    Coordination Polymers, Depolymerisation, Dinuelear Copper Complexes, Diastereomers, X-Ray 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-1410.pdf 
 Identifier    ZNB-1994-49b-1410 
 Volume    49 
5Author    Angela Bayler, Andreas Bauer, Hubert SchmidbaurRequires cookie*
 Title    Chiral Phosphine Ligands in the Structural Chemistry of Gold  
 Abstract    The reaction of chloro(dimethylsulfide)gold(I) with (2-hydroxybutyl)diphenylphosphine (L) (racemic mixture) in dichloromethane affords high yields of the racemic chiral complex (L)AuCl. Metathesis reactions with KBr or KI, respectively, in a two-phase solvent mix­ ture (CH2CI2/H2O) lead to a conversion into the corresponding bromide and iodide complexes (L)AuBr and (L)AuI. Treatment of silver chloride with the ligand L in acetonitrile yields the analogous 1:1 adduct (L)AgCl. The compounds have been characterized by their analytical and spectroscopic data, and the structures of (L)AuCl and (L)AuBr have been determined by single-crystal X-ray diffraction. The compounds build isomorphous crystal lattices (monoclinic, P2i/c) in which pairs of enantiomers (R-and S-configuration of L) are aggregated by two long hydrogen bonds between the hydroxyl group of the ligand and the halogen substituent of the neighbouring molecule. Cationic, linear two-coordinate 1:2 complexes (L)2Au+ X-(X = BF4, CIO4, SO3CF3) and (L)2Ag+ X-(X = BF4) are obtained in good yields by reaction of L with Me2SAuCl and AgX (molar ratio 2:1:1) or with AgBF4 (molar ratio 2:1), respectively. 31P NMR studies at variable temperature show an equilibrium between all possible stereoisomers (RR, SS, RS, SR) in solution with rapid ligand exchange at ambient temperatures. 
  Reference    Z. Naturforsch. 52b, 1477—1483 (1997); received October 14 1997 
  Published    1997 
  Keywords    Gold Complexes, Phosphane Complexes, Chiral Phosphanes, Crystal Structure, Diastereomers 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-1477.pdf 
 Identifier    ZNB-1997-52b-1477 
 Volume    52