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  • Inorganic carbon-free chelate rings  (1)
  • Organo-phosphorus compounds  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2327-2333 
    ISSN: 1434-1948
    Keywords: Heterocycles ; Organo-phosphorus compounds ; Dithiadiphosphetane disulfides ; Phosphonates ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New salts of thionated (naphthalene-1,8-diyl)bis(phosphonic) acid monoanhydrides [PPh4+]2[C10H6PS2(μ-S)PS22-] (2) and [K+]2[C10H6PS2(μ-S)POS2-]·H2O (3) both containing the C3P2S ring, were prepared in high yields by the reaction of 2,4-(naphthalene-1,8-diyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (1) with NaHS and PPh4Cl, or KOH, respectively, in water. The derivative 3, containing a P=O terminal bond as well as P-S-P bridge, undergoes, in acid conditions, a rearrangement reaction leading to the O,S-symmetrically substituted derivative [K+]2[C10H6PS2(μ-O)PS22-] (4) containing a C3P2O heterocycle. Dipotassium salt 4 was converted into the bis(tetraphenylphosphonium) salt 5 by the treating with PPh4Cl. Hydrolysis of [PyH+][C10H6P(S)(NHMe)(μ-S)PS22-] (15) led to [CH3NH3+][PyH+][C10H6POS(μ-O)POS2-]·1.5 Py (6). New compounds were characterised by 31P{1H}-, 1H- and 13C{1H}-NMR, FT-IR, ES-MS and in the cases 2-6 by X-ray structure determination. The 31P{1H}-NMR spectra of these mixed O,S-derivatives are briefly discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Phosphazene metallacycles ; [N-(Diphenylphosphinoselenoyl)-P,P-diphenylphosphinoselenoic amidato-Se,Se′] chelates ; Inorganic carbon-free chelate rings ; Octahedral MSe6 core (M = Sb, Bi, and In) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The [(SePPh2)2N]- ligand 1c forms stable tris(chelates) with the SbIII, BiIII, and InIII ions. The crystal and molecular structures of the resulting compounds 3, 4, and 5 were determined by X-ray diffractometry. The coordination geometry around the metal centers can be described as a distorted octahedron. This feature and the results obtained by comparing the structures with their sulfur and oxygen analogs lead us to conclude that in both SbIII and BiIII compounds the arrangement around the metals suggests a stereochemically nonactive electron lone pair.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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