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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 6 (1987), S. 2313-2318 
    ISSN: 1520-6041
    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 Institute of Physics (AIP)
    Journal of Applied Physics 60 (1986), S. 130-136 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report an application of nuclear magnetic resonance (NMR) spectroscopy to the study of fluorine-doped silicate glass prepared by the modified chemical vapor deposition process, prior to drawing the rod into fibers. The silica contains 1.03-wt. % fluorine, as determined by the calibrated intensity of the 19F NMR spectrum. The isotropic chemical shift of the 19F spectrum shows that fluorine bonds only to silicon; there is no evidence of oxyfluorides. Analysis of the distribution of nuclear dipolar couplings between fluorine nuclei reveals that the relative populations of silicon monofluoride sites [Si(O–)3F] and species having near-neighbor fluorines, such as silicon difluoride sites [Si(O–)2F2], are nearly statistically random. That is, to a good approximation, the fluorine substitutes randomly into the oxygen sites of the silica network. There is no evidence of local clusters of fluorine sites, silicon trifluoride sites [Si(O–)F3], or silicon tetrafluoride (SiF4).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 58 (1985), S. 197-203 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: In this study, 31P nuclear magnetic resonance spectra of phosphorus-doped silica have been analyzed to determine the concentration, chemical bonding and spatial distribution of phosphorus. The silica samples were prepared as performs for optical waveguide fibers. The two samples examined contained 1.12±0.02 and 0.06±0.02 wt. % phosphorus. Comparison with the profile of the refractive index shows that a nominal 1.0 wt. % phosphorus increases the refractive index 0.055% relative to pure fused silica. A single, well-defined 31P chemical shielding powder pattern is observed which implies that one species of phosphorus is dominant. Based on the 31P isotropic chemical shift and the magnitude and orientation of the shielding anisotropy, the phosphorus species is interpreted to be P(O) (O−)3. That is, the phosphorus is pentavalent and forms one terminal P=O bond and three bridging P-O− bonds. The distribution of phosphorus-phosphorus internuclear distances, determined from the 31P spin-echo data, indicates that phosphorus is randomly substituted into the silica network: there is no evidence of phosphate clusters.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 69-88 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Decomposition studies of trichlorosilane, dichlorosilane, and monochlorosilane at 921 K, 872 K, and 806 K, respectively, are reported. The studies were made at fixed reactant pressures over a range of total pressures in a wall conditioned, quartz reactor connected to a quadrupole mass-spectrometer. Products were monitored sequentially and continuously in time. The dichlorosilane decomposition was also studied by the comparative-rate single-pulse shock-tube method at temperatures around 1250 K. Two mechanisms of decomposition are considered: a silylene based mechanism initiated by molecular elimination reactions (Scheme I), and a free radical based mechanism initiated by bond fission reactions (Scheme V). Modeling tests of these mechanisms show that only the former is consistent with the experimental data. The decompositions are shown to be essentially nonchain processes initiated by the following pressure dependent reactions: HSiCl3(SINGLEBOND)4→ SiCl2+HCl, H2SiCl2(SINGLEBOND)1→ SiCl2+H2 and H3SiCl(SINGLEBOND)5→ HSiCl+H2. High pressure Arrhenius parameters recommended for these reactions are A4,∞=A1,∞=A5,∞=1014.5±0.5 s-1, E4,∞=71.9±2.1 kcal/mol, E1,∞=69.2±2.0 kcal/mol, and E5,∞=60.6±1.8 kcal/mol. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet: 30: 69-88, 1998.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 89-97 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Data relative to methane trapping of SiCl2 and a rate constant for the SiCl2 into C(SINGLEBOND)H bond insertion process of k-1=13.4 M-1s-1 at 921 K are reported. Results on the decomposition of the trapping product, methyldichlorosilane, are also reported. This decomposition follows first-order kinetics with a rate constant of k=1.5±0.2×10-3 s-1 at 905 K and produces methane, trichlorosilane, methyltrichlorosilane, and tetrachlorosilane. It is argued that the decomposition involves silylene intermediates, is nonchain, and is initiated primarily by the molecular methane elimination process MeSiHCl2(SINGLEBOND)1→ CH4+SiCl2. Free radicals and Si(SINGLEBOND)C bond fission may also contribute to the decomposition but are not dominant. The kinetics of MeSiHCl2 decomposition are shown to be consistent with the kinetics of the reverse SiCl2/CH4 trapping reaction and with the overall reaction thermochemistry. Reaction modeling gives product yields, reactant conversions, and rates in reasonable agreement with the data. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 89-97, 1998.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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