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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 117 (1995), S. 5160-5161 
    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
    Organometallics 13 (1994), S. 3399-3401 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 641-646 
    ISSN: 0009-2940
    Keywords: Gold ; S ligands ; Carboxylato complexes ; Thioether complexes ; Sulfonium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of 2-mercaptoaniline with {[(Ph3P)Au]3O}+ BF-4 leads to a regioselective auration to give the (2-aminophenyl)sulfonium complex {(2-H2NC6H4S[Au(PPh3)]2}+ BF-4 (1) as the sole product. With the same reagent, 4-hydroxyphenyl)sulfonium salt 2, and 2-mercaptopyridine is converted into the 2-pyridylsulfonium salt 3. Dinuclear auration of the thiol functions is thus clearly favoured over the reaction at any of the other functional groups (-NH2, -py, -OH). As shown in earlier work, this is also true for HS-functional carboxylic acids. With an excess of the oxonium reagent, however, 2-mercaptosuccinic acid was now found to be converted into a tetranuclear complex with a doubly aurated sulfonium group and monoaurated carboxylate functions (4). Bis(2-mercaptoethyl) ether and thioether react with the oxonium salt to give tetranuclear bis(sulfonium salts) 5, 6, with bifurcated {-S[Au(PPh3)]2}+ groups at both ends. Structural studies of compounds 1, 5 and 6 showed the cations to be aggregated into centrosymmetrical dimers through short Au-Au contacts. Compound 5 forms one-dimensional infinite chains through a similar aggregation via the two bifurcated sulfonium end groups of each individual dicationic unit. The dications of compound 6 are associated only into centrosymmetrical dimers leaving one of the two sulfonium groups of each unit without auriophilic contacts to neighbouring dications, probably owing to an internal Au-S contact with the thioether function.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 565-567 
    ISSN: 0009-2940
    Keywords: Antimony, tris(dimethylphenylsilyl)- ; Antimony, trisilyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tris(dimethylphenylsilyl)antimony (1) was prepared in moderate yield from dimetallic “Na3Sb” (generated in situ) and chlorodimethylphenylsilane in tetrahydrofuran at reflux temperature. The product was identified by standard analytical and spectroscopic techniques, and the crystal structure was determined by single-crystal X-ray diffraction (triclinic, space group P1, Z = 2). The SbSi3 skeleton is pyramidal (average Si-Sb-Si angle 100.2°, average Sb-Si bond length 2.558 Å), and the Me2PhSi groups are in a staggered conformation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 907-909 
    ISSN: 0009-2940
    Keywords: Gold(I) thiolates ; (1,2-Ethanedithiolato)gold(I) complexes ; (tert-Butanethiolato)gold(I) complexes ; Polynuclear gold(1) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of tert-butanethiol with tris[(triphenylphosphane)gold(I)]oxonium tetrafluoroborate in dichloromethane in the presence of sodium tetrafluoroborate gave quantitative yields of a product {Me3CS[Au(PPh3)]2}+ BF-4 (1). In the crystal lattice of this salt, the sulfonium cations are associated into dimers through close Au…Au contacts. The centrosym-metrical tetranuclear unit has Au…Au distances of 3.292(1) and 3.206(1) Å, and the Au-S-Au angles are exactly 90.0(1)°. Both data are indicative of significant intra- and intercationic Au…Au attractions. The analogous reaction of ethane-1, 2-dithiol afforded high yields of a product {(CH2S)2[Au(PPh3)]3}+ BF-4 (2). The compound is fluxional in CD2Cl2 solution and shows only one 31P-NMR signal at -60°C. In the crystal, the quasi C2-symmetrical trinuclear cations feature the sulfur atoms in bridging positions between two gold atoms. The central gold atom is thus three-coordinate; the peripheral gold atoms are two-coordinate with Au…Au contacts at 3.284(1) and 3.129(1) Å and Au-S-Au angles as small as 86.5(1) and 81.0(1)°. This provides clear evidence for “auriophilic” bonding.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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