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  • 1
    ISSN: 1572-8927
    Keywords: Nitrogen-15 ; NMR ; praseodymium-nitrate complexes ; water-acetone mixtures ; contact ion-pairing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A direct, low-temperature nitrogen-15(15N) NMR technique has been applied to the study of inner-shell complex formation between praseodymium(III) and nitrate ion in aqueous solvent mixtures. In water-acetone mixtures at −95°C, ligand exchange is slow enough to permit the observation of15N NMR signals for uncomplexed and coordinated nitrate ion, but satisfactory resolution is obtained only by the addition of Freon-12 to these systems for study at −110 to −115°C. Four coordinated nitrate signals are generally observed and a very small signal for an additional complex, or an isomer of one of the others, appears at the highest nitrate concentrations. Signals for the mono-and dinitrato complexes are unambiguously identified, but with the exception of the trinitrato complex, several possibilities exist for the remaining peaks. To overcome excessive viscosity signal broadening, measurements in methanol and ethanol are possible only with praseodymium trifluoromethanesulfonate (triflate). Coordinated nitrate signals in aqueous and anhydrous methanol are observed only for the mono-and dinitrato species, and signal areas indicate a maximum of two moles of nitrate per Pr(III) are complexed. A third signal is evident in the ethanol solution spectra, and the presence of this higher complex was confirmed by area measurement of the fraction of bound nitrate. The extent of complex formation in these solvent systems is attributed to differences in the dielectric constant. A comparison of the complexing tendencies of Pr(III) to other ions studied by this NMR method suggests the possibility of a coordination number change across the lanthanide series. Preliminary15N NMR results for metal-ion complexes with the isothiocyanate ion are presented.
    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: 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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  • 4
    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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