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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. 476-481 
    ISSN: 0749-1581
    Keywords: Electron paramagnetic resonance ; Electron spin resonance ; Metal carbonyl radical ; Iron-tungsten carbonyl ; Unpaired electron ; g Matrix ; Odd-electron carbonyl ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Single crystals of PPN+HFeW(CO)9- prepared from THF · W(CO)5 and PPN+HFe(CO)4- exhibit weak single-line EPR spectra corresponding to the presence of two paramagnetic impurities. One of the spectra increases in intensity by an order of magnitude on 60Co γ-irradiation. The g2 matrices for both species in an orthogonal crystal-axis system were assembled from measurements of g values made at 77 K on crystallographically oriented samples. The intense spectrum has principal g values of 2.0064, 2.0468 and 2.1320 and principal directions of g which lie close to bonds emanating from the Fe nucleus of the undamaged anion. Consideration of the principal g values and directions for this species leads to an assignment to a FeW(CO)9- radical in which the unpaired electron is principally located in a Fe 3dz2 orbital directed along the Fe—H bond of the host anion. The other signal has principal g values (2.0229, 2.0425, 2.0950) close to those established for the singly bridged isomer of Fe2(CO)8-, but their directions do not correlate well with bond directions within the host anion. It is concluded that small amounts of the persistent Fe2(CO)8- radical generated in the preparative procedures substitute for the host anion in the crystals of PPN+HFeW(CO)9-.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0749-1581
    Keywords: NMR ; substituent-induced chemical shifts ; 2-N-acetamido-2-deoxy-β-D-glucopyranosides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The additive behaviour generally observed for the substituent-induced chemical shifts (SCS) for disubstituted benzenes was examined for a series of aryl 2-N-acetamido-2-deoxy-β-D-glucopyranosides having a wide range of para substituents with varying possible electronic contributions. The SCS values associated with non-acetylated and peracetylated glucoside rings in para-substituted aryl 2-N-acetamido-2-deoxy-β-D-glucopyranosides were calculated. The additive nature of SCS analysis for para-substituted systems was shown to hold for the meta and para positions but the very small change in chemical shifts for the ortho positions precluded attempts at analysis of these data. The observation of a good correlation for the ipso carbons for the acetylated compounds compared with a poor correlation for the same site in the non-acetylated compounds is not well understood.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0749-1581
    Keywords: Molecular motion ; Carbon-13 relaxation ; Octyl chains ; Polydecene ; Model lubricants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C nuclear relaxation behaviour of n-alkyl chains in a variety of compounds can be described in terms of two relaxation times, one for tumbling (τc) and one for each carbon nucleus for the internal motions (τc). Relaxation data for the quaternary carbon nuclei of n-octylbenzene and n-octyl cyanide have been used to determine τc) and their activation energies [Ea(τc)]. These values have enabled τe and their associated activation energies [Ea(τe)] to be calculated for each carbon in the alkyl chains of the two compounds. In these compounds the values for C-6 appear to be invariant with τe(298) = 15 ± 2 ps and Ea(τc) = 15 ± 1 kJ mol-1. Assuming that these are universal values for all n-octyl chains, we have used them to calculate τe and Ea(τe) for other simple n-octyl compounds, thus allowing τc and E.a(τc) to be determined. It was found that Ea(τc) values correlate well with those for Ea(n/T) obtained from viscosity measurements. Di-n-octyl ether shows motional properties similar to those of the straightchain compounds.Simultaneous fitting of relaxation rate and NOE enhancement data measured over a range of radiofrequencies and temperatures permits a wealth of motional properties to be discerned when there is a suitable frequency dispersion. Both tri-n-octylamine and polydecene tumble sufficiently slowly to allow both relaxation rate and NOE data to be used to evaluate τc and τe and their activation energies without making any assumptions about C-6. The values of τc(298) and Ea(τc) obtained from C-6 for tri-n-octylamine are 314 ± 12 ps and 18.5 ± 0.4 kJ mol-1, respectively, and the corresponding values for polydecene are 576 ± 41 ps and 16.1 ± 1.3 kJ mol-1, respectively.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. 852-858 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; 3J(CH) ; Glucopyranosides ; Aryl 2-acetamido-2-deoxy-β-D-glucopyranosides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 13C NMR spectra of twenty aryl 2-acetamido-2-deoxy-β-D-glucopyranosides and eighteen aryl 3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-β-D-glucopyranosides have been obtained and assigned. The three-bond proton coupling constants of these compounds were also obtained.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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