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'Amine Complexes' in keywords Facet   section ZfN Section B  [X]
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1998 (1)
1997 (1)
1Author    PeterG. Jones, Birte AhrensRequires cookie*
 Title    Gold(I)-Komplexe mit Aminliganden, II [1]. (Methylpyridin)-Komplexe von Gold(I) Gold(I) Complexes with Amine Ligands, II. Methylpyridine Complexes of Gold(I)  
 Abstract    Gold(I) complexes of overall formula LAuCl (L = various methylpyridines) are non-con­ ducting in acetone. X-ray structure analyses show that the solid state structure of the cor­ responding complex 1 (L = 2-picoline) is molecular; the 3-picoline derivative 2 is however ionic (L2A u)+(AuCl2)-. 3-Picoline forms a molecular complex LAuC6F5 (3) and also the ionic (L2Au)+(SbF6)_ (4). Complexes 1, 2 and 4 display short A u--A u contacts, leading to chains of gold atoms; additionally, complexes 3 and 4 show weak Au-F contacts. The (3-picoline)-gold(III) complex /rans-(L2AuCl2)+(SbF6)_ (5) was obtained as a by-product; it too contains short Au-F contacts. 
  Reference    Z. Naturforsch. 53b, 653—662 (1998); eingegangen am 6. April 1998 
  Published    1998 
  Keywords    Gold(l), Pyridine, Amine Complexes, X-Ray Data 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0653.pdf 
 Identifier    ZNB-1998-53b-0653 
 Volume    53 
2Author    JoséM. López-De-Luzuriaga, Marcus Söldner, Annette Schier, Hubert SchmidbaurRequires cookie*
 Title    Gold(I) Complexes of Open-chain and Cyclic Di-secondary Amines  
 Abstract    Treatment of N,N'-diisopropyl-ethylenediamine or 1,4-piperazine with two equivalents of [(Ph^P)Au]+ BF4-leads to binuclear complexes of the diamines: {[(Ph3P)Au]HN('Pro)NCH2-}22+ 2 BF4~ (1) and {[(Ph3P)Au]HNCH2CH2}22+ 2 BF4~ (2), respectively. In the products each quaternary ammonium center bears one gold ligand, one hydrogen atom and two alkyl substituents. The crystal structures of both compounds have been determined. Compound 1 contains discrete ion-triples. The ethylene bridge in the dications is in an unfolded conformation, with a crystallographic center of inversion, and allows for weak hydrogen bonding N-H--F [2.085 A; N-H--F 169.2°] between the NH functions and the counterions. The existing distant contacts F-A u [3.599 A] are probably less significant for the aggregation of the ion triples, but will contribute through Coulomb forces. Compound 2 crystallizes with two solvent molecules CH2CI2. The dication has a crystallographic center of inversion with the piperazine ring in a chair conformation and the gold atoms in equatorial positions. There are hydrogen bonds N-H--F [2.076 and 2.457 A] between the dication and the anions which lead to the formation of ion-triples, with further contacts between the BF4~ anions and the solvent molecules [C-H--F 2.340 and 2.446 A]. 
  Reference    Z. Naturforsch. 52b, 209—213 (1997); received December 4 1996 
  Published    1997 
  Keywords    Gold(I) Coordination, Amine Complexes, Secondary Amines, Ammonium Complexes 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0209.pdf 
 Identifier    ZNB-1997-52b-0209 
 Volume    52