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  • 1
    Publication Date: 1991-02-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 2
    Publication Date: 1991-03-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 593 (1991), S. 61-68 
    ISSN: 0044-2313
    Keywords: Palladium Cluster Compounds, Pd9-Cluster ; Syntheses ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses and Crystal Structures of [Pd9As8(PPh2)8] and [Pd9Sb6(PPh3)8][PdCl2(PPh3)2] reacts with As(SiMe3)3 to give the new cluster [Pd9As8(PPh3)8] (4). 4 has been characterized by X-ray crystal structure analysis. It is a molecule in which four [Pd2(PPh3)2]-units are bridged by As2-units. A further Pd atom is located in the centre of the cluster. 4 crystallizes in the space group C2/c with four formula units per unit cell. The lattice constants at 200 K are: a = 3 970.6(3), b = 1 648.90(16), c = 3 266.30(20) pm, β = 131,44(4)°. The reaction of [PdCl2(PPh3)2] with Sb(SiMe3)3 yields [Pd9Sb6(PPh3)8] (5). 5 consists of a body centred cubic Pd9-cluster. All of the cube faces are capped by μ4-Sb-ligands. 5 crystallizes in the space group Pn3 with two formula units per unit cell. The lattice constants at 200 K are: a = b = c = 1 995.4(2) pm.
    Notes: [PdCl2(PPh3)2] reagiert mit As(SiMe3)3 zu der neuen Clusterverbindung [Pd9As8(PPh3)8] (4). Die Struktur von 4 wurde durch eine Kristallstruktruanalyse aufgeklärt. Danach besteht das Molekül aus vier [Pd2(PPh3)2]-Einheiten, die durch As2-Brücken verbunden sind. Im Zentrum des Clusters befindet sich zudem noch ein weiteres Pd-Atom. 4 kristallisiert in der Raumgruppe C2/c mit vier Formeleinheiten in der Elementarzelle. Die Gitterkonstanten betragen bei 200 K: a = 3 970,6(3), b = 1 648,90(16), c = 3 266,3(20) pm, β = 131,44(4)°. Die Reaktion von [PdCl2(PPh3)2] mit Sb(SiMe3)3 führt dagegen zu [Pd9Sb6(PPh3)8] (5). In 5 liegt ein raumzentrierter Kubus von 9 Pd-Atomen vor. Alle Flächen des Kubus werden von μ4-Sb-Liganden überbrückt, und acht Pd-Atome sind zunächst an PPh3-Liganden gebunden. 5 kristallisiert in der Raumgruppe Pn3 mit zwei Molekülen in der Elementarzelle. Die Gitterkonstanten betragen bei 200 K: a = b = c = 1 995,4(2) pm.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0044-2313
    Keywords: Tris(di-tert-butylphospha)heptaphosphanortricyclane, (t-Bu2P)3P7 ; Tris(di-tert-butylstiba)heptaphosphanortricyclane, (t-Bu2Sb)3P7 ; syntheses ; crystal structure ; 31{1H} n.m.r. data ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [t-Bu2P]3P7 and (t-Bu2Sb)3P7, as well as Investigations on the Formation of Heptaphosphanes (3) Containing PMe2, PF2, and P(CF3)2 GroupsTris(di-tert-butylphospha)heptaphosphanortricyclane (t-Bu2P)3P7 1 obtained by reacting Li3P7 · 3 DME with t-Bu2PF forms yellow crystals. (t-Bu2Sb)3P7 2 produced similarly from t-Bu2SbCl and Li3P7 · 3 DME didn't form crystals; it decomposes in a solution of toluene above -10°C. Both compounds were identified by their 31P{1H} NMR spectra, and 1 also by elemental analysis and single crystal structure determination (space group) P21/a, a = 1 712.0(9) pm, b = 1 105.1(7) pm, c = 1 854.0(10) pm, β = 94.96(4)°, Z = 4 formula units in the elementary cell).Attempts to synthesize (Me2P)3P7 3, (F2P)3P7 4 and [(F3C)2P]3P7 5 failed as dialkylchlorophosphanes as Me2PCl e. g. with Li3P7 · 3 DME react under Li/Cl exchange, dialkylfluorophosphanes (except t-Bu2PF) disproportionate, and neither PF3 nor (F3C)2PBr with Li3P7 · 3 DME give the desired products 4 or 5, resp.
    Notes: Tris(di-tert-butyl-phospha)-heptaphosphanortricyclan (t-Bu2P)3P7 1 entsteht durch Umsetzung von Li3P7 · 3 DME mit t-Bu2PF und bildet gelbe Kristalle. Das analog aus t-Bu2SbCl und Li3P7 · 3 DME gebildete (t-Bu2Sb)3P7 2 wurde nicht kristallin erhalten. Es zersetzt sich in Lösung (Toluol) oberhalb -10°C. Der Nachweis von 2 erfolgt über das 31P{1H}-NMR-Spektrum, der von 1 anhand des 31P{1H}-NMR-Spektrums, der Analyse und der Kristallstrukturbestimmung. 1 kristallisiert in der Raumgruppe P21/a mit Z = 4 Formeleinheiten; a = 1 712,0(9) pm, b = 1 105,1(7) pm, c = 1 854,0(10) pm, β = 94,96(4)°.Untersuchungen zur Bildung von (Me2P)3P7 3, (F2P)3P7 4, [(F3C)2P]3P7 5 führten nicht zum Ziel, weil Dialkylchlorphosphane wie Me2PCl (zur Bildung von 3) mit Li3P7 · 3 DME unter Li/Cl-Austausch reagieren, Dialkylfluorphosphane (ausgenommen t-Bu2PF) disproportionieren und PF3 sowie (F3C)2PBr mit Li3P7 · 3 DME nicht zu den Verbindungen 4 und 5 führen.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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