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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 107-112 
    ISSN: 1434-1948
    Keywords: Silicon ; Aminosilanes ; Aziridine ; Azetidine ; Molecular conformation ; Configuration determination ; Nitrogen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a continuation of structural investigations of poly(amino)silanes, a series of silicon derivatives of aziridine and azetidine have been prepared. Analogies with the isoelectronic phosphorus ylide species and the high barrier to inversion at nitrogen in small N heterocycles were suggestive of steeply pyramidal and rather rigid configurations at the N atoms in the title compounds. Tetrakis(N-aziridino)silane (1) and tetrakis(N-azetidino)silane (2) have been synthesized from SiCl4 and LiN(CH2)x (x = 2, 3). Compound 1 is also formed when LiN(CH2)2 and HSiCl3 are used as starting materials, but with free aziridine a non-volatile product (1a) is obtained. In neither case could any trace of HSi[N(CH2)2]3 be detected. In contrast, RSiCl3 (R = Me, Ph) could readily be converted into the corresponding tris(N-aziridino)silanes (3, 4) by treatment with excess aziridine. Tris(N-azetidino)silane (5) was accessible from HSiCl3 and excess azetidine, but the product was found to contain an unknown impurity. In order to determine the local symmetry and the dynamics of the aziridine rings, 1H-NMR spectra were recorded at low temperature (-80°C). No splitting of the signals was observed, indicating that the inversion barriers are extremely low, even in the highly strained three-membered heterocycles. Nevertheless, single-crystal X-ray diffraction studies of the N-triphenylsilyl derivatives of aziridine (6) and azetidine (7) revealed an aziridinyl group with a steeply pyramidal configuration at nitrogen in 6 (sum of the angles at N 313.32°), and an azetidinyl group with a flat geometry in 7 (sum of the angles at N 350.96°). The Si-N bond is significantly shorter in 7 as compared to that in 6.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1167-1174 
    ISSN: 0009-2940
    Keywords: Silicon ; Configuration determination ; Aminosilanes ; Tetra(amino)silanes ; Molecular conformation ; Conformation analysis ; Nitrogen ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a search for crystalline homoleptic tetra(amin)silanes with (mirror)-symmetrical NR2 substituents, tetrakis( 1-pyrrolidinyl)silane (1) was prepared by an improved synthetic route, and tetrakis(morpholino)silane (2) was synthesized from SiBr4 and morpholine/Li-morpholide via the intermediate BrSi[N(CH2CH2)2O]3 (4). With SiCl4 only the monochloro stage, 3, is reached. Tetrakis(4-methyl-1-piperazinyl)silane (5) was prepared similarly, using 4-methylpiperazine. With (CH2)6NH or (CH2)6NLi and SiBr4 only [(CH2)6N]3SiBr (6) was obtained. The structures of 1, 2 and 5 were determined by single-crystal X-ray diffraction. While compound 1 has an irregular molecular geometry following no symmetrical pattern, molecules of 2 and 5 have similar structures with almost superimposable Si(NC2)4 cores of approximate D2d symmetry. The overall molecular symmetry of 2 is reduced only by incongruous folding of the heterocycles, which are all in a chair conformation. The core structures of 2 and 5 are in excellent agreement with the results of density function calculations for Si(NH2)4. Si(NMe2)4 (the crystal structure of which could not be determined) was converted into (Me2N)3SiO-SO2CF3 (7) by treatment with two equivalents of triflic acid. Reaction of 7 with 1-naphthylamine/triethylamine affords (Me2N)3SiNHC9H7 (8). With 2,4-difluoroaniline/NEt3 the analogous derivative (Me2N)3SiNHC6H3F2 (9) is obtained, but with 4-bromoaniline the product is a silane with the ligands redistributed to give (Me2N2),Si(NHC6H4Br), (10), the structure of which was also determined. It has a non-standard geometry with very flat nitrogen pyramids at all four substituents.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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