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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    British journal of dermatology 98 (1978), S. 0 
    ISSN: 1365-2133
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Antisera to human oral epithelial cells were produced in rabbits and found to be specific for epithelial type cells of man, guinea-pig and rabbit. Binding of the antisera to human oral epithelial cells was not affected by pre-incubation in concanavalin A, trypsin or neuraminidase, nor by pre-incubation of the antisera with fetuin. The antisera would appear to differ from pemphigus antiserum.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8927
    Keywords: Carbon-13 ; nitrogen-15 ; NMR ; samarium-nitrate complexes ; samarium-isothiocyanate complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The extent of inner-shell, contact ion-pairing between samarium(III)-nitrate and in a preliminary manner, samarium(III)-isothiocyanate, has been determined by a direct, low-temperature, multinuclear magnetic resonance technique. In water-acetone mixtures containing Freon-12 or Freon-22, the slow exchange condition is achieved at −110 to −120°C, permitting the observation of15N NMR resonance signals for bulk and coordinated nitrate. In these mixtures, signals are observed for Sm(NO3)2+, Sm(NO3) 2 + , and two higher complexes, possibly the tetranitrato with either the penta-or hexanitrato.1H NMR signals for bound water molecules in these mixtures were observed, but accurate hydration numbers can not yed be determined. In anhydrous or aqueous methanol mixtures,15N NMR signals for only three complexes are observed, with the dinitrato clearly dominating. Using15N and35Cl NMR chemical shift and linewidth measurements, the superior complexing ability of nitrate compared to perchlorate and chloride, was demonstrated. Successful preliminary13C and15N NMR measurements of Sm3+-NCS− interactions in water-acetone-Freon-22 mixtures also have been made. The13C NMR spectra reveal signals for five complexes, presumably Sm(NCS)2+ through Sm(NCS) 5 2− . In the15N NMR spectra, signals for only three complexes are observed (the result of insufficient spectral resolution.) displaced about +240 ppm from bulk anion.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-8927
    Keywords: Hydrogen-1 ; carbon-13 ; nitrogen-15 ; NMR ; lutetium(III) ; isothiocyanate ; complexation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A direct, low-temperature hydrogen-1, carbon-13, and nitrogen-15 nuclear magnetic resonance study of lutetium(III)-isothiocyanate complex formation in aqueous solvent mixtures has been completed. At −100°C to −120°C in water-acetone-Freon mixtures, ligand exchange is slowed sufficiently to permit the observation of separate1H,13C, and15N NMR signals for coordinated and free water and isothiocyanate ions. In the13C and15N spectra of NCS−, resonance signals for five complexes are observed over the range of concentrations studied. The13C chemical shifts of complexed NCS− varied from −0.5 ppm to −3 ppm from that of free anion. For the same complexes, the15N chemical shifts from free anion were about −11 ppm to −15 ppm. The magnitude and sign of the15N chemical shifts identified the nitrogen atom as the binding site in NCS−. The concentration dependence of the13C and15N signal areas, and estimates of the fraction of anion bound at each NCS−:Lu3+ mole ratio, were consistent with the formation of [(H2O)5Lu(NCS)]2+ through [(H2O)Lu(NCS)5]2−. Although proton and/or ligand exchange and the resulting bulk-coordinated signal overlap prevented accurate hydration number measurements, a good qualitative correlation of the water1H NMR spectral results with those of13C and15N was possible.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-8927
    Keywords: Hydrogen-1 ; carbon-13 ; nitrogen-15 ; NMR ; magnesiumisothiocyanate complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A hydrogen-1, carbon-13, and nitrogen-15 NMR study of magnesium(II)-isothiocyanate complexation in aqueous mixtures has been completed. At temperatures low enough to slow proton and ligand exchange, separate1H,13C, and15N NMR signals are observed for coordinated and bulk water molecules and anions. The1H NMR spectra reveal signals for the hexahydrate and the mono-through triisothiocyanato complexes, as well as two small signals attributed to [Mg(H2O)5(OH)]1+ and [Mg(H2O)4(OH)(NCS)]. Accurate hydration numbers were obtained from signal area integrations at each NCS− concentration. In the15N NMR spectra, signals also were observed for the mono-through triisothiocyanato complexes, and a small signal believed to be due to [Mg(H2O)4(OH)(NCS)]. Coordination number contributions for NCS− were measured from these spectra and when combined with the hydration numbers they totalled essentially six at each anion concentration. Signals for [Mg(H2O)5(NCS)]1+ through [Mg(H2O)3(NCS)3]1− also were observed in the13C NMR spectra and the area evaluations were comparable to the15N NMR results. An analysis of the magnitude and sign of the coordinated NCS− chemical shifts identified the nitrogen atom as the anion binding site. All spectra indicated [Mg(H2O)5(NCS)]1+ and [Mg(H2O)4(NCS)2] were the dominat isothiocyanato complexes over the entire range of anion concentrations. The inability to detect evidence for complexes higher than the triisothiocyanato reflects the competitive binding ability of water molecules and perhaps the decreased electrostatic interaction between NCS− and negatively charged higher complexes.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-8927
    Keywords: Carbon-13 ; nitrogen-15 ; NMR ; europium-nitrate complexes ; europium-isothiocyanate complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A direct, low-temperature nuclear magnetic resonance spectroscopic study of europium(III)-nitrate contact ion-pairing has been completed, and preliminary results for europium(III)-isothiocyanate have been obtained. In water-acetone-Freon mixtures, at −110°C to −120°C, four15N NMR signals are observed for coordinated nitrate ion. Area evaluations of the signals and their concentration dependence indicate the formation of Eu(NO3)2+, Eu(NO3) 2 1+ , and two higher complexes, possibly the tetra-, with either the penta-or hexanitrato. This correlates well with similar15N NMR results obtained for Ce(III), Pr(III), Nd(III), and Sm(III). As a result of a higher dielectric constant, complex formation is significantly less in water-methanol mixtures, wheein only three complexes form with Eu(NO3) 2 1+ dominating at the highest anion concentrations. Competitive complexing experiments in water-methanol also were made by35Cl NMR chemical shift and linewidth measurements, as well as15N NMR. Initial experiments with the Eu3+-NCS− system show four coordinated anion signals, displaced from the bulk anion peak by about −250 ppm and −2,500 ppm in the13C and15N NMR spectra, respectively. Area evaluations are consistent with the presence of Eu(NCS)2+ through Eu(NCS) 4 1- in these solutions. A consideration of the chemical shifts identified the nitrogen atom as the site of binding in the NCS−. A discussion of these preliminary results, as well as those for several other metal-ions, will be presented.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0749-1581
    Keywords: NMR ; 1H NMR ; 13C NMR ; 15N NMR ; 27Al NMR ; isothiocyanate ; complexes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A multinuclear magnetic resonance (NMR) study of the complexes of aluminum(III) with isothiocyanate ion in water-acetone mixtures has been completed. At temperatures low enough to slow proton and ligand exchange, separate resonance signals are observed for coordinated and bulk H2O (1H) and NCS- (13C, 15N), and Al3+ (27Al) in each complex. The 1H NMR spectra reveal six sets of signals for the complexes, [Al(H2O)6]3+ through [Al(H2O)(NCS)5]2-, including isomers for three of the species. Signal area measurements show a decrease in the Al3+ hydration number with increasing NCS- concentration, as this anion replaces water in the solvation shell. In the 27Al NMR spectra of these systems, signals for seven complexes, [Al(H2O)6]3+ through [Al(NCS)6]3-, are observed, with chemical shifts increasing by about 6 ppm with each additional NCS-. Although broadened somewhat by the Al(III) quadrupole, the 13C and 15N NMR spectra also reveal coordinated NCS- signals for these complexes, including 27Al—N13CS J-coupling in [Al(NCS)6]3-. Area evaluations of the 15N NMR signals provide an excellent complement to the 1H hydration number data. These NMR results demonstrate that a multinuclear approach to the study of solution complexes can provide detailed structural information about the species being formed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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