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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 841-844 
    ISSN: 0009-2940
    Keywords: N-Silylanilines ; Anilines, N-silylated ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new N-(arylsilyl)anilines 1-5 have been obtained by the reaction of aryl(halo)silanes with the corresponding anilines in the presence of the auxiliary base triethylamine. The benzene parts of the anilines have been chosen such that their fluoro, methyl, and methoxy substituents exert different electronic effects. The molecular structures of the monosilylated anilines 3 and 4 have been determined by single-crystal X-ray diffraction analysis. The coordination geometry of the nitrogen atoms have been found to be planar. Heteronuclear NMR spectra (1H, 13C, 15N, 29Si) have been recorded and the structural results correlated with the one-bond coupling constant 1J(29Si15N).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: 1,8-Disilylnaphthalene ; Disiloxane ; Disilthiane ; Disilazanes ; Phosphonium bis(silyl)methylide based on 1,8-disilylnaphthalene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis, spectroscopic data and molecular structures of heterocycles derived from 1,8-disilylnaphthalene are reported. The key intermediate for the preparation of the title compounds is 1,8-bis[(trifluoromethylsulfonyl)silyl]naphthalene (3), which is prepared from 1,8-bis[(4-methoxyphenyl)silyl]naphthalene (2) by treatment with two equivalents of triflic acid in toluene at -20°C. The resulting silyl triflate is stable only below this temperature and was not isolated. Its reactions with water, ammonia, amines, and sulfane give the corresponding disiloxane, disilazanes and disilthiane. The molecular structure of Si,Si′-(Naphthalene-1,8-diyl)-N-phenyldisilazane (8) was determined by X-ray diffraction. Treatment of 2 with substoichiometric amounts of triflic acid and subsequent reaction of the resulting monosilyl triflate with tert-butylamine gives a related chiral N-tert-butyl-Si-(4-methoxyphenyl)disilazane 10. Its molecular structure was proven by X-ray diffraction. A cyclic phosphonium bis(silyl)methylide (11) was synthesized by a transylidation process using 3 and CH2=P(NMe2)3. The structure of 11 was also determined by X-ray diffraction.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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