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  • NMR  (9)
  • Wiley-Blackwell  (9)
  • American Association for the Advancement of Science
  • Annual Reviews
  • International Union of Crystallography (IUCr)
  • 1990-1994  (9)
  • 1955-1959
  • 1994  (9)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 2803-2807 
    ISSN: 0887-624X
    Keywords: copolymer sequence ; NMR ; methyl methacrylate ; styrene ; α-trifluorome-thacrylic acid ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [no Abstrat]
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1585-1592 
    ISSN: 0887-6266
    Keywords: NMR ; polymer networks ; distribution of chain lengths ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel technique for the analysis of the distribution of chain lengths between crosslink junctions of polymer networks is proposed. The technique is based on the relation between the high-temperature nuclear magnetic resonance free-induction decay and the network structure. The distribution functions are determined for a number of networks. In particular, the evolution of structure of a thermally degrading network is studied. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; Conformation ; Ab initio calculations ; 1-cis-Methoxy-1,3-trans-butadiene ; 1-trans-Methoxy-1,3-trans-butadiene ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton-coupled 13C NMR spectra of 1-trans-methoxy- (2) and 1-cis-methoxy-1,3-trans-butadiene (3) are consistent with a methoxy heavy atom planar conformation with s-syn and s-anti orientations, respectively. Ab initio 6-31G* calculations confirmed such conformations. They were taken as model compounds to determine the influence of electrostatic interactions on the methoxy 13C NMR parameters. A shielding increase of 4 ppm is observed in 2, with respect to 3, for the OMe 13C chemical shift in an s-syn conformation and is ascribed to the attraction between the methyl and vinyl moieties as proposed by Li and Chesnut. The methyl 1J(C,H) coupling is not affected by this interaction, showing that the carbon 2p electrons are more polarizable than those in the 2s orbital.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 335-342 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; Conformational analysis ; Coupling constants ; NOE ; Non-steroidal anti-inflammatory drugs ; Mefenamic acid ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR spectra of the non-steroidal anti-inflammatory drugs mefenamic acid, meclofenamic acid and flufenamic acid were assigned and the solution dynamics and conformations of the compounds were probed by the analysis of NMR chemical shifts, temperature coefficients, 3J(C,H) coupled constants, nuclear Overhauser enhancement (NOE) effects and saturation transfer experiments. At low concentrations the anthranilic acid derivatives (the fenamates) exist as monomer units with intramolecular hydrogen bonding between the amine proton and the carboxylic acid group. At concentrations of 10 mM and above, solution aggregates exist. The intermolecular association does not disrupt the intramolecular N—H…O=C hydrogen bonding, resulting in a similar conformation for mefenamic and flufenamic acids at both low and high concentrations. Meclofenamic acid has an additional intramolecular hydrogen bond, resulting in a slightly different conformation to the other two fenamates. The results from this conformational study are of potential value in molecular and pharmacophore modelling studies on the bioactive conformations of these drugs.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 446-451 
    ISSN: 0749-1581
    Keywords: NMR ; 14N ; NMR ion-exchange membrane ; NH4+ ; Quadrupolar splitting ; Spin-lattice relaxation ; Nafion ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 14N NMR Spectroscopy of NH4+ is a convenient and sensitive probe of structure and mobility in Nafion, Dow and Neosepta cation-exchange membranes. NH4+ ions bound to these commercially produced membranes give rise to small 14N quadrupolar splittings ranging from 10 to 160 Hz. Moderate stretching of Nafion and Dow membranes induces much larger splittings of up to 2 kHz. The splitting has also been found to be dependent on the orientation of the membranes in the magnetic field B0. In Nafion it reaches a minimum at an angle of 45-55° between the direction of stretch and B0. The quadrupolar splittings also increase with increase in temperature. 14N spin-lattice relaxation times in all three membranes at 300 K are about 20 times shorter than in aqueous solution, consistent with strongly bound NH4+ ions. The apparent activation energies for 14N relaxation, derived from the temperature dependence of the T1, data, show that reorientation of the bound NH4+ ions requires ca. 20 kJ mol-1 in Nafion and Dow membranes and ca. 30 kJ mol-1 in Neosepta, compared with 6.5 kJ mol-1 for free NH4+ in aqueous solution.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 242-247 
    ISSN: 0749-1581
    Keywords: NMR ; Isotope shift ; 19F,129Xe chemical shifts ; Xe,F coupling constants ; Xenon difluoride ; Krypton difluoride ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of the various xenon and krypton isotopes on the nuclear shielding of 19F in xenon and krypton difluoride in solution were studied by 19F NMR spectroscopy. For both molecules, linear relationships were observed between the one-bond secondary isotope shift of the 19F nucleus, 1Δ; 19F(m′/128Xe) and 1Δ 19F(m′/78Kr), and the relative mass factor, (m′ - m)/m′, and also between the shifts and the quadratic mean bond displacement, 〈(Δr)2〉. On the basis of the latter correlation and the linear relationship between 〈Δr〉 and 〈(Δr)2〉 for the linear combination of the first and second derivatives of the 19F shielding, the values -1742 and -5804 ppm Å-2, respectively, were determined. Further, the temperature dependence of the 129Xe and 19F chemical shifts and the 129Xe, 19F indirect spin-spin coupling of XeF2 were determined. The 129Xe chemical shift is extremely sensitive to temperature with Δδ/ΔT = -0.4718 ppm K-1, whereas for 19F Δδ/ΔT = +0.0042 ppm K-1. In contrast, the 129Xe, 19F indirect spin-spin coupling is independent of temperature over the range 243-303 K, the mean value being 5644.2 ± 0.6 Hz.
    Additional Material: 5 Ill.
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  • 7
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; Deuterium isotope effects ; Benzanilides ; Cross-conjugated transmission ; Substituent effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deuterium isotope effects on 13C nuclear shielding, nΔC(D), transmitted across a D-labelled nitrogen atom were investigated for a series of para-substituted benzanilides. The two two-bond isotope shifts, 2ΔC(D) are perturbed essentially in a trough-bond manner by change of the contribution of mesomeric structures. The magnitudes of 2Δ(C=O) and 2Δ(C-1′) are found to be mutually interdependent as evidenced by the linear relationships between the average values of 2Δ(C=O) and 2Δ(C-1′) with 1H(NH) chemical shifts and with 15N SCS. This behaviour is interpreted as resulting from a cross-conjugated transmission pathway involving the carbons sharing the D-labelled nitrogen.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 330-334 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; NOE ; 4-Amino-(D3)-trishomocubanes ; Biological activity ; Configuration ; Stereochemistry ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Amino compounds of the highly symmetrical (D3)-trishomocubane were recently shown to possess promising biological activities, i.e. antiviral and antiparkinson. This series was synthesized via a modified Ritter reaction. The unique hydrocarbon skeleton of these compounds has a D3 point group symmetry with a propeller shape. Several geometrical isomers are possible for the derivatives of (D3)-trishomocubane. This paper reports the complete 1H and 13C NMR assignments and the configuration at C-4 of one of the most promising compounds of the present series, i.e. 3-phenyl-4-amino-(D3)-trishomocubane. The 13C NMR spectrum of this amine indicates the presence of only one geometrical isomer for the compound. NOE experiments on the fully assigned 1H NMR spectrum show that this isomer has the 3S4S/3R4R configuration, and not the 3S4R/3R4S configuration. These results indicate that the Ritter rearrangement proceeds stereospecifically and that it provides a facile method for the synthesis of (D3)-trishomocuban-4-amines from tertiary alcohols of pentacyclo[5.4.0.02,6.03,10.05,9] undecan-8-ol.
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 561-563 
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; Substituted ; naphthalenes ; Deoxyhemigossypol ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 13C NMR spectra of the deoxyhemigossypol derivatives 4-isopropyl-2,3-dimethoxy-6-methylnaphthalene, 4-isopropyl-2,3-dimethoxy-6-methyl-1-naphthaldehyde and 2,3-dihydroxy-4-isopropyl-6-methyl-1-naphthaldehyde were assigned using one- and two-dimensional NMR techniques, including DEPT, 1H NOE and 1H—13C HETCORR spectroscopy.
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