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'Solid State Structures' in keywords Facet   Publication Year 1999  [X]
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1Author    Joachim Heinickea, Attila Dala, Hans-Friedrich Kleinb, Olaf Hetcheb, Ulrich Flörkec, Hans-Jürgen HauptcRequires cookie*
 Title    Formation of r71-P-(2-Phosphinophenol)Ni(0)(PMe3)3 and Oxidation to cjs/fraws-Bis(2-phosphinophenolato)nickel(II) Complexes  
 Abstract    o-Phosphinophenols 1 (P ^ O H) react with equimolar amounts of Ni(PMe3)4 at low tempera­ tures to give yellow Ni(0) complexes such as [(HO~P)Ni(PMe3)3] 2a with only P coordination of the P ^ O H ligand. Oxidation of solutions of 1 and Ni(PMe3)4 by dioxygen leads to brown bis(o-phosphinophenolato-P^O)nickel chelate complexes 3a-d. Structure elucidation by NM R is consistent with a m-square planar geometry for 3a-c and a rrans-square planar solution struc­ ture of the terr-butylphenylphosphino derivative 3d. The geometric isomers were distinguished by different ranges of phosphorus coordination shifts and 3lP-l3C-2 and 3IP-13C-1 coupling 
  Reference    Z. Naturforsch. 54b, 1235—1243 (1999); received May 19 1999 
  Published    1999 
  Keywords    Phosphinophenolate, Nickel, Complexes, Structure Elucidation, Solid State Structures 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-1235.pdf 
 Identifier    ZNB-1999-54b-1235 
 Volume    54 
2Author    Silke Buchler, Franc Meyer, Albrecht Jacobi, Peter Kircher, Laszlo ZsolnaiRequires cookie*
 Title    Novel Dinucleating Ligand Systems Containing Two Adjacent Coordination Compartments of the Potential Triamidoamine-Type -Nickel(II) and Cobalt(II) Coordination Chemistry  
 Abstract    The preparation of novel dinucleating pyrazolate ligands H5L3 -H5L8 carrying chelating side arms with appending secondary amine functions is reported. Following different synthetic routes, either CH2CF3, C6H2F3 , or CftF? moieties can be introduced as substituents at the termi­ nal nitrogen atoms. These systems are reminiscent of two coupled coordination compartments of the potential triamidoamine-type. Crystallographic analyses of a series of bimetallic complexes of the CH2CF3-substituted ligand H5L4 with NiCh and C0 CI2 reveal manifold coordination modes in the solid state, resulting from the facile detachment of a single or several N-donor sites from the metal centers. Coordination number sets {4/6} (in H5L4Co2CU) and {5/6} (in H4L4Ni2Cl3, H4L4Co2Cl3 and H5L4Ni2CL) are thus observed. In the non-deprotonated HsL-type systems the remaining protons are found to be scavenged by a pyrazolate-N (in H5L4Ni2CU) or an amine function of a ligand side arm (in H ^ C o iC U). 
  Reference    Z. Naturforsch. 54b, 1295—1306 (1999); received June 18 1999 
  Published    1999 
  Keywords    Dinuclear Complexes, N-Ligands, Nickel, Cobalt, Solid-State Structures 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-1295.pdf 
 Identifier    ZNB-1999-54b-1295 
 Volume    54