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  • 1
    ISSN: 0044-2313
    Keywords: Silicon ; germanium ; tin compounds, phosphanes ; tetramethylcyclopentadienyl ; carbonyl complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Dimethyl(tetramethylcyclopentadienyl)silyl-, -germyl-, and -stannylphosphanes. X-Ray Structures of Chloro(dimethyl)tetramethylcyclopentadienyl-stannane and Tetracarbonyl[1-dimethyl(tetramethylcyclopentadienyl)germyl-3,4-dimethyl-phospholene]iron(0)Me2Cp′SiCl (1) (Cp′ = C5HMe4) reacts with magnesium and R2PCl (R = Ph, tBu) as well as PCl3 in tetrahydrofurane yielding Me2Cp′SiPPh2 (4), Me2Cp′SiPtBu2 (5) and (Me2Cp′Si)3P (6) respectively. The reaction of Me3SiPPh2 (7) or Me3SiPC4H4Me2 (10) with Me2Cp′GeCl (2) and Me2Cp′SnCl (3) leads to the formation of Me2Cp′EPPh2 (E = Ge (8), Sn (9)) and Me2Cp′EPC4H4Me2 (E = Ge (11), Sn (12)). 11 reacts with Fe(CO)5 with formation of Fe(CO)4[(PC4H4Me2)GeCp′Me2] (13). 3 crystallizes in the space group P21/n with a = 986,7(1), b = 1247,3(2), c = 1028,2(1) pm, β = 92,71(1)°, Z = 4 and V = 1264,1(2) 10-30 m3. The final refinement resulted in R1 = 0,0249 for 2097 observed reflexions with Fo ≥ 4σ(Fo). 13 crystallizes in the space group P21/n with a = 967,7(3), b = 1298,70(16), c = 1832,7(3) pm, β = 95,810(19)°, Z = 4 and V = 2291,4(8) 10-30 m3 (R1 = 0,0444 for 4043 observed reflexions with Fo ≥ 4σ(Fo). 13 forms a trigonal bipyramide with the phosphane ligand 11 in an axial position.
    Notes: Me2Cp′SiCl (1) (Cp′ = C5HMe4) reagiert mit Magnesium und R2PCl (R = Ph, tBu) bzw, PCl3 in Tetrahydrofuran unter Bildung von Me2Cp′SiPPh2 (4) und Me2Cp′SiPtBu2 (5) bzw. (Me2Cp′Si)3P (6). Durch Umsetzung von Me3SiPPh2 (7) oder Me3SiPC4H4Me2 (10) mit Me2Cp′GeCl (2) und Me2Cp′SnCl (3) wurden Me2Cp′EPPh2 (E = Ge (8), Sn (9)) bzw. Me2Cp′EPC4H4Me2 (E = Ge (11), Sn (12)) erhalten. 11 reagiert mit Fe(CO)5 unter Bildung von Fe(CO)4[(PC4H4Me2)GeCp′Me2] (13). 3 kristallisiert in der Raumgruppe P21/n mit a = 986,7(1), b = 1247,3(2), c = 1028,2(1) pm, β = 92,71(1)°, Z = 4 und V = 1264,1(2) 10-30 m3 (R1 = 0,0249 für 2097 beobachtete Reflexe mit Fo ≥ 4σ(Fo). 13 kristallisiert in der Raumgruppe P21/n mit a = 967,7(3), b = 1298,70(16), c = 1832,7(3) pm, β = 95,810(19)°, Z = 4 und V = 2291,4(8) 10-30 m3 (R1 = 0,0444 für 4043 beobachtete Reflexe mit Fo ≤ 4σ(Fo). 13 ist trigonal bipyramidal mit dem Phosphanliganden 11 in axialer Position.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 571-572 
    ISSN: 0044-2313
    Keywords: Trimethylsilyl phosphines ; trimethylgermyl phosphines ; trimethylstannyl phosphines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1-Trimethylsilyl-, 1-Trimethylgermyl-, and 1-Trimethylstannyl-3,4-dimethylphospholene1-Lithium-3,4-dimethylphospholen reacts with Me3SiCl and Me3GeCl yielding 1-trimethylsilyl-3,4-dimethylphospholene (1) and 1-trimethylgermyl-3,4-dimethylphospholene (2) respectively. 2 and 1-trimethylstannyl-3,4-dimethylphospholene (3) are formed using the reaction of 1 with Me3GeCl and Me3SnCl respectively. The 1H, 13C and 31PNMR-spectra as well as the mass spectra of the new compounds are discussed.
    Notes: 1-Lithium-3,4-dimethylphospholen reagiert mit Me3SiCl und Me3GeCl unter Bildung von 1-Trimethylsilyl-3,4-dimethylphospholen (1) bzw. 1-Trimethylgermyl-3,4-dimethylphospholen (2). 2 und 1-Trimethylstannyl-3,4-dimethylphospholen (3) werden durch Umsetzung von 1 mit Me3GeCl bzw. Me3SnCl erhalten. Die neuen Verbindungen wurden durch 1H-,13C- und 31P-NMR-Spektren sowie durch Massenspektren charakterisiert.
    Type of Medium: Electronic Resource
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