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'Triphenylphosphine' in keywords Facet   section ZfN Section B  [X]
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1999 (1)
1975 (1)
1Author    Requires cookie*
 Title    New Synthesis of N-phosphoranylidene-sulfuric Aeid Amides, -sulfuric Acid Alkylester Amides, -fluoro- sulfuric Acid Amide and -alkylsulfonamide, I I 1-2  
 Abstract    By reaction of triphenylphosphine and carbon tetrachloride with methane sulfon­ amide (la) and the sulfamic acid derivatives 
  Reference    (Z. Naturforsch. 30b, 134—135 [1975]; eingegangen am 2. Oktober 1974) 
  Published    1975 
  Keywords    Triphenylphosphine, Carbon Tetrachloride, Sulfamic Acid Derivatives, Methane Sulfonamide 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0134_n.pdf 
 Identifier    ZNB-1975-30b-0134_n 
 Volume    30 
2Author    KonstantinV. Domasevitcha, ElenaG. Petkovaa, Alexander Yu, VeraV. Nazarenkob, Joachim Ponomareva3, N.Kent Sielerc, EduardB. Dalleyb, Rusanov3Requires cookie*
 Title    Antimony as a Donor Atom in Silver Coordination Chemistry: Synthesis, IR Spectra and Structure of the Silver(I) Cyanoximate Complexes with Triphenylstibine and Triphenylphosphine Model Compounds  
 Abstract    Silver(I) cyanoximate complexes Ag{ONC(CN)-R} (R = COPh, {L1}; COC(CH3)3, {L2}; benzothiazol-2-yl, {L3}) with triphenylphosphine and -stibine of compositions Ag(PPh3)n{L} (n = 2, 4) and Ag(SbPh3)n{L} (n = 3 for {L1} and {L2}, n = 2 for {L3}) were synthesized by the reaction of the components in acetonitrile solution and characterized by elemental analyses and IR spectroscopy. The crystal structures of Ag(SbPh3)3{L} (L = {L } (1), { L2} (2), Ag(SbPh3)2{L3} CH3CN (3) and Ag(PPh3)2{L '}C H 3CN (4), have been determined by X-ray diffraction. For all the compounds examined the coordination environment of the silver atom has the geometry of a distorted terahedron ([AgP2NO] (4); [AgSb3N] (1), (2); [AgSb2N2] (3)). The bis adducts Ag(EPh3)«{L} adopt molecular structures, in which the organic anions are coordinated in bidentate chelate fashion via the nitroso nitrogen atom and the oxygen (nitrogen for { L3}) atom of the substituent R. In the fm-stibino complexes (Ag-Sb 2.670(4) -2.7748(8) A; Sb-Ag-Sb 108.87(4) -115.00(2)°) the cyanoximates are unidentate ligands and coordinated via the nitroso nitrogen atoms (Ag-N ca. 2.35(1) A). The different behaviour of N ,0 and N,N chelating cyanoximes under the same conditions suggests, that the Sb donor triphenylstibine is able to substitute the oxygen atoms in the silver(I) coordination sphere, but not the nitrogen ones. This causes the formation of 1:3 adducts of Ag{L} with SbPh3 for N ,0 donors {L 1} and {L2}, and only 1:2 for N,N donor anionic {L3}. 
  Reference    Z. Naturforsch. 54b, 904—912 (1999); received December 15 1998 
  Published    1999 
  Keywords    Silver, Triphenylphosphine, Triphenylstibine, Cyanoximes, X-Ray Data 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-0904.pdf 
 Identifier    ZNB-1999-54b-0904 
 Volume    54