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  • Analytical Chemistry and Spectroscopy  (3)
  • 17O variable pressure NMR  (1)
  • Imaging agents  (1)
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  • 1
    ISSN: 1434-1948
    Keywords: Imaging agents ; Lanthanides ; NMR spectroscopy ; DNA cleavage ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydration state of a series of [Ln(DO2A)(H2O)n]+ complexes in aqueous solution at pH = 6.4-7.0 was studied by measuring the lanthanide-induced 17O shifts (LIS) of water [Ln includes elements from Ce to Yb; DO2A = 1,7-bis(carboxymethyl)-1,4,7,10-tetraazacyclododecane]. Their contact contribution, obtained from Reilley plots, indicated a decrease in the inner-sphere water coordination number of the [Ln(DO2A)(H2O)n]+ complexes from n = 3 (Ce-Eu), to n = 2 (Tb-Yb). A temperature-dependent UV/Vis absorption study of the 578-582 nm 7F0 → 5D0 transition band of [Eu(DO2A)(H2O)n]+ in aqueous solution showed that this complex is present in an equilibrium between eight- and nine-coordinate species with n = 2 and n = 3, respectively. The hydration equilibrium parameters (2 ↔ 3), K2-3298 = 4.0 ± 0.2, ΔH2-30 = -12.1 ± 1 kJ mol-1 and ΔS2-30 = -28.9 ± 3 J mol-1 K-1,correspond to an average hydration number of 2.65-2.85 in the temperature range 273-363 K. A variable temperature, multiple field 17O NMR study combined with direct EPR measurements of the transverse electronic relaxation rates has been used to obtain the parameters characterizing water exchange, rotation and electronic relaxation, all influencing the proton relaxivity of [Gd(DO2A)(H2O)2-3]+. The small increase in the water exchange rate of [Gd(DO2A)(H2O)2-3]+ (kex298 = (10 ± 5) × 106s-1) relative to that of[Gd(DOTA)(H2O)]- (4.8 × 106 s-1) is a consequence of an unfavorable interplay of charge and hydration equilibria. The value of τR298 = 40 ± 1 ps is short, and the electronic relaxation rate (1/T2e ≍ 1.2 × 1010 s-1) is fast relative to [Gd(DOTA)(H2O)]- (1.3-2.4 × 109 s-1 for B = 0.34 T). These parameters negate to some extent the expected increase in proton relaxivity of the [Gd(DO2A)(H2O)2-3]+ complex.Supporting information for this article is available on the WWW under -//_/_http://www.wiley-vch.de/contents/jc_2005/2000/99338_s.pdf or from the author.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0749-1581
    Keywords: Hexaaquarhodium(III) ; 17O variable pressure NMR ; Water exchange ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants and activation parameters for water exchange on hexaaqua- and monohydroxypentaaquarhodium(III) were determined by 17O NMR as a function of temperature (323-364 K) and pressure (up to 210 MPa, at 323 K) at several acidities (1.0-5.0 molal HClO4). The observed rate constant was of the form kex = k1 + k2/[H+], where the subscripts 1 and 2 refer to the exchange pathways on Rh(H2O)63+ and Rh(H2O)5(OH)2+, respectively. The kinetic parameters are as follows: k1298 = 2.2 × 10-9 s-1, ΔH1
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0749-1581
    Keywords: 17O NMR ; Gd3+ ; Variable pressure ; Water exchange ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 17O NMR longitudinal and tranverse relaxation rates and chemical shifts were measured at variable temperature at three magnetic fields (1.4, 4.7 and 9.4 T) for aqueous solutions of the complexes [Gd(H2O)8]3+ and [Gd(PDTA)(H2O)2]-. The transverse relaxation rates and chemical shifts were analysed in the light of recent EPR line width measurements to obtain the parameters for water exchange kinetics: kex298 = (8.30 ± 0.95) × 108 and (1.02 ± 0.10) × 108 s-1, ΔH
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 32 (1994), S. 739-745 
    ISSN: 0749-1581
    Keywords: NMR ; 17O ; Nd3+ ; Pr3+ ; Water exchange ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 17O NMR relaxation rate measurements were made on aqueous perchlorate solutions of the light lanthanide ions Nd3+ and Pr3+, with the aim of measuring the kinetics of water exchange on these ennea aqua ions. Variable-temperature results at three magnetic fields show that the ‘kinetic’ effect is not the only contribution to the difference between the transverse and longitudinal relaxation rates. The results at high magnetic field allow lower limits, kex298 ≥ 5 × 108 S-1 and kex298 ≥ 4 × 108 s-1, to be determined for water exchange rates at 298.15 K on [Nd(H2O)9]3+ and [Pr(H2O)9]3+, respectively. These limits are consistent with our current understanding of water exchange on the lanthanide aqua ions, based on the change of relative stability of the ennea and octa aqua ions across the series.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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