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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 107 (1985), S. 8043-8049 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemical reviews 93 (1993), S. 1623-1667 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemical reviews 94 (1994), S. 1273-1297 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 1766-1767 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 3519-3524 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus, 41. Synthesis and Reactions of Phenyl-trimethylsilyl-phosphineThe trimethylsilylation of potassium phenylphosphide with trimethylchlorosilane leads in 60% yield to the mixed-substituted secondary phosphine 1, not described before. It reacts with potassium in polar or non-polar solvents to give the salt 2 that forms an adduct 2·2 CS2 with carbon disulphide. The reaction of 1 with equimolecular amounts of bromine or N-bromosuccinimide does not lead to the silylated halogenophosphine 4. The P—Si-bond being quantitatively cleaved, trimethylbromosilane and „phenylphosphorus“ of various molecular weight are formed.
    Notes: Bei der Trimethylsilylierung von Kaliumphenylphosphid mit Trimethylchlorsilan entsteht in 60proz. Ausbeute das bisher nicht bekannte gemischt-substituierte sekundäre Phosphin 1. Es reagiert mit Kalium in polaren oder unpolaren Solventien zu dem Salz 2, das mit Schwefelkohlenstoff ein Addukt 2·2 CS2 bildet. Die Umsetzung von 1 mit äquimolaren Mengen Brom bzw. N-Brom-succinimid führt nicht zu dem silylierten Halogenphosphin 4. Unter quantitativer Spaltung der Phosphor-Silicium-Bindung werden Trimethylbromsilan und „Phenylphosphor“ unterschiedlicher Molekülgröße gebildet.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 1000-1003 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Sulphuryl Chloride with Triethylamine: a Simple Method for the Preparation of N.N-Diethyl-(1.2.2-trichlorovinyl)amineSulphuryl chloride (1) reacts with triethylamine (2) even at -15° in ether to give the chlorination product N.N-diethyl-(1.2.2-trichlorovinyl)amine (3), 2·SO2, and 2·HCl. Besides a small amount of the unknown N.N-diethyl-(2.2.2-trichloroethyl)amine hydrochloride (4) is formed. An adduct of 1 and 2 or the formation of ethyl chloride have not been observed.
    Notes: Sulfurylchlorid (1) reagiert mit Triäthylamin (2) bereits bei -15° in Äther unter Chlorierung zu Diäthyl-(1.2.2-trichlor-vinyl)-amin (3), 2 · SO2 und 2 · HCl. Daneben entsteht in geringer Menge das bisher nicht bekannte Diäthyl-(2.2.2-trichlor-äthyl)-amin-hydrochlorid (4). Ein Addukt aus 1 und 2 oder die Bildung von Äthylchlorid waren nicht feststellbar.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 3844-3849 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus, 48Synthesis of Tetraorganyldiphosphanes and Mercury Bis(di-tert-butylphosphide)Tetraorganyldiphosphanes, R4P2, are formed in 91-96% yield by the reaction of secondary alkyl-, cycloalkyl-, and arylphosphines with di-tert-butylmercury. The reaction proceeds via the mercury bis(diorganylphosphides), Hg(PR2)2, not described before. As the first compound of this class, the tert-butyl derivative 4 was isolated. It is surprisingly stable against oxidation and thermal decomposition, but is easily converted into the corresponding diphosphane by photolysis. As spectroscopic data indicate, the phosphorus-mercury bond in 4 has a considerable double-bond character.
    Notes: Tetraorganyldiphosphane, R4P2, entstehen bei der Umsetzung von sekundären Alkyl-, Cycloalkyl- und Arylphosphinen mit Di-tert-butylquecksilber in 91-96proz. Ausbeute. Die Reaktion verläuft über die bisher nicht bekannten Quecksilber-bis(diorganylphosphide), Hg(PR2)2. Als erster Vertreter wurde die tert-Butyl-Verbindung 4 isoliert, die oxidativ und thermisch überraschend beständig ist, photolytisch aber leicht in das entsprechende Diphosphan umgewandelt werden kann. Nach spektroskopischen Befunden weist die Phosphor-Quecksilber-Bindung in 4 einen beträchtlichen Doppelbindungsanteil auf.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3970-3971 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2404-2405 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 1264-1271 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Phosphorus, 88. 1,2,3-Triphenyl-1,3-bis(trimethylsilyl)triphosphaneThe reaction of 1,3-dipotassium 1,2,3-triphenyltriphosphide, K2 (PPh)3, with chlorotrimethyl-silane yields the hitherto unknown title compound Me3Si(Ph)P—P(Ph)—P(Ph)SiMe3 (1), which is remarkably stable against disproportionation reactions. In solution it forms the three diastereomers 1a (erythro/erythro), 1b (erythro/threo), and 1c (threo/threo) in a ratio of about 8:3:1, between which a dynamic equilibrium exists due to pyramidal inversion at the P-atoms. The correlation between the 31P-NMR-spectroscopically observed spin systems and the diastereomers 1a-c results from the significant dependence of the 1JPP-coupling constants on dihedral angles. The preferred trans arrangement of the bulky SiMe3- and P(Ph)SiMe3 groups at adjacent P-atoms leads to a trans-conformation of the lone electron pairs in the erythro- and to a gauche-conformation in the threo-configuration.
    Notes: Die Reaktion von 1,3-Dikalium-1,2,3-triphenyltriphosphid, K2(PPh)3, mit Chlortrimethylsilan ergibt in guter Ausbeute die bislang unbekannte Titelverbindung Me3Si(Ph)P—P(Ph)—P(Ph)SiMe3 (1), die gegenüber Disproportionierungsreaktionen bemerkenswert beständig ist. Sie bildet in Lösung die drei Diastereomeren 1a (erythro/erythro), 1b (erythro/threo) und 1c (threo/threo) im Verhältnis von etwa 8:3:1, die infolge pyramidaler Inversion der P-Atome in einem dynamischen Gleichgewicht miteinander stehen. Die Korrelation zwischen den 31P-NMR-spektroskopisch beobachteten Spinsystemen und den Diastereomeren 1a-c ergibt sich aufgrund der signifikanten Torsionswinkelabhängigkeit der 1JPP-Kopplungskonstanten. Die bevorzugte trans-Anordnung der großvolumigen SiMe3- und P(Ph)SiMe3-Reste an benachbarten P-Atomen führt bei erythro-Konfiguration zu einer trans- und bei threo-Konfiguration zu einer gauche-Konformation der freien Elektronenpaare.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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