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  • crystal structure  (1)
  • thermal stability  (1)
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  • 1
    ISSN: 1572-8862
    Schlagwort(e): silver ; amidines ; diphenylamidines ; tetrameric ; C-alkylamidines ; thermal stability ; imaging ; thermographic ; photothermographic
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau , Physik
    Notizen: Abstract N,N′−Diphenylamidines and the silver(I) complexes of their deprotonated anions have been synthesized. Previously uncharacterized tetrameric structural motifs were produced by the inclusion of alkyl substituents at the amidinate carbon. The addition of a 2-methoxy functional group to the phenyl ring resulted in a cationic silver trimer in which hydrogen bonding links silver(I)-bound water molecules to the methoxy substituents. The thermal stabilities of the tetrameric species vary with alkyl chain length. The new complexes are: tetrakis(N,N′-diphenylpropamidinato) tetra silver(I), 1, tetrakis(N,N′-diphenylbutamidinato) tetrasilver(I) 2, tetrakis(N,N′-diphenylpentamidinato) tetra silver(I) 3, (N,N′-diphenyloctamidinato)silver(I) 4, (tetrakis(N,N′-di(4-n-butyl)phenylpropamidinato)tetrasilver(I), 5, bis(N,N′-di(2-methoxy)phenylacetamidinato)diaquatrisilver(I) nitrate 6 and tetrakis(N,N′-di(4-methoxy)phenylacetamidinato) tetrasilver(I), 7. Compounds 1, 5, 6 and 7 were structurally characterized by X-ray methods.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1572-8854
    Schlagwort(e): Silver ; stearate ; triphenylphosphine ; crystal structure
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Geologie und Paläontologie , Physik
    Notizen: Abstract The crystal and molecular structure of [bis-triphenylphosphine-silver(I) stearate], [((C6H5)3P)2Ag(O2C(CH2)16CH3)], has been determined by single crystal X-ray analysis: the space group is PT witha=12.021(4),b=13.916(5)1,c=14.678(5) Å, α=95.952(5), β=101.249(6), γ=93.259(5)°,V=2388(2) Å3, andD calc=1.293 g/cm3 forZ=2. The silver is four coordinate: the carboxylate symmetrically chelates the silver while the triphenylphosphine ligands occupy the third and fourth coordination sites. The strong bonding nature of the phosphine ligands, as indicated by the Ag−P bond lengths, 2.446(3) and 2.424(3) Å, dominates the coordination sphere of the silver and forces the initial carboxylate ligand to rearrange from bridging to chelating resulting in weaker Ag−O bonds, as indicated by the extended Ag−O bond lengths, 2.399(8) and 2.449(8) Å. Unlike the free acid, the long hydrocarbon chain is not linear, and exhibits disorder in the lattice. The structure of the title complex explains the dramatic shift in solubility properties compared to the starting phosphine free silver carboxylate.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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