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  • sodium-23 NMR  (4)
  • Monensin  (2)
  • crown ethers  (2)
  • 1
    ISSN: 1572-8927
    Keywords: N-methylformamide ; nonaqueous solvents ; preferential solvation ; isosolvation point ; sodium-23 NMR
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Sodium-23 NMR chemical shifts and linewidths have been measured for 0.1M NaClO4 in binary mixtures of N-methylformamide (NMF) with a series of other solvents, as a function of the solvent mole fraction. The relative solvent composition at the isosolvation point, the mid-value of the Na-23 chemical shift between those measured in the respective pure solvents, reveals preferential solvation of the sodium cation in many cases. The isosolvation composition correlates well with the relative solvating abilities of the two solvents-as characterized by their donicities-provided that the cation-solvent interactions are of the ‘hard-hard’ type and that they are not complicated by interionic interactions. The variation in the electric field gradient around the sodium nucleus, as the composition of the solvent changes, results in broadening of the resonance line. Maximum broadening occurs close to the solvent mole fraction corresponding to the isosolvation point.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 7 (1978), S. 357-372 
    ISSN: 1572-8927
    Keywords: Monensin ; antibiotic ionophores ; alkali complexes ; thallium(l) complex ; Silver(l) complex ; stability constants ; entropy of complexation ; enthalpy of complexation ; nonaqueous solvents ; potentiometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Potentiometric and cyclo-voltammetric studies have been carried out on monensin anion (Mon−) complexes with the alkali ions as well as with Tl+ and Ag+ in absolute methanol solutions. The log Kf values obtained for the complexity constants and corrected for the activity effects are: Li+, 3.3±0.1; Na+, 6.72±0.05; K+, 5.18±0.05; Rb+, 4.58±0.05; Cs+, 3.75±0.05; Tl+, 5.31±0.05; Ag+, 8.2±0.2. It is seen that for the alkali, the most stable complex is formed with Na+. The enthalpy and entropy of complexation with the sodium ion were found to be ΔHo=−5.47±0.24 kcal-mole−1 and ΔSo=+12.4±0.7 e.u. The complex, therefore, is enthalpy and entropy stabilized.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 8 (1979), S. 83-95 
    ISSN: 1572-8927
    Keywords: Monensin ; alkali metal complex ; silver complex ; thallium complex ; potentiometry ; enthalpy of complexation ; entropy of complexation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The acid-base and complexing properties of a naturally occurring antibiotic ionophore-monensin (MonH)-were studied in anhydrous methanol solutions primarily by potentiometric measurements. The pK a of the acid was found to be 10.30±0.05 at 25°C. Complexes of silver, thallium, and alkali ions with the undissociated ligand were also studied, and their stability constants were determined. The acid dissociation constant of MonH as well as the stability constants of Mon− Na+ and MonH·NaClO4 complexes were determined in the 5–45°C temperature range, and the enthalpy and entropy of the acidity and stability constants were determined from van't Hoff's plots. The formation of MonH and Mon−Na+ species are both enthalpy and entropy stabilized, but the formation of the MonH·NaClO4 complex is enthalpy stabilized but entropy destabilized.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 11 (1982), S. 17-26 
    ISSN: 1572-8927
    Keywords: Zinc-67 NMR ; nonaqueous solution ; zinc complexes ; crown ethers ; EDTA ; methanol ; dimethylformamide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Solutions of zinc salts in water, methanol (MeOH), dimethylformamide (DMF) and binary mixtures of water with the two nonaqueous solvents were studied by zinc-67 NMR measurements. Anhydrous zinc nitrate solutions in DMF and MeOH show upfield, concentration independent, chemical shifts at −27 and −19 ppm, respectively, vs. the aqueous solution standard. Addition of DMF or MeOH to an aqueous solution of a zinc salt results in a diamagnetic shift but for the addition of acetonitrile a paramagnetic shift results. In all cases the signal was broadened very considerably, e.g., in ZnCl2 solution the linewidth increased from ∼40 to ∼600 Hz in going from water to 35% aqueous MeOH. Both67Zn and13C NMR failed to show any complexation of Zn2+ ion by crown ethers in aqueous solution. A gradual addition of EDTA, of diaza-18-crown-6 or of tetraazacyclotetradecane resulted in an immediate broadening of the67Zn signal which became undetectable when one equivalent of a ligand was added.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-8927
    Keywords: Lithium-7 NMR ; sodium-23 NMR ; cesium-133 NMR ; far infrared ; alkali complexes ; cryptates ; formation constants ; nonaqueous solvents ; membranes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Nuclear magnetic resonances of alkali nuclei,7Li,23Na, and133Cs, as well as far infrared measurements are used to study alkali complexes of a bicyclic diazapolyoxa ligand—the dilactam of cryptand C222. Measurements were carried out in pyridine, tetrahydrofuran, acetonitrile, nitromethane, dimethylformamide, and aqueous solutions. The complexing ability of the dilactam is similar to, but weaker than, that of the cryptand C222. The limiting chemical shifts of the complexed cations were solvent-dependent, indicating incomplete enclosure of the cation by the ligand. Formation constants of Li+ and Cs+ complexes were calculated from the chemical-shift dependence on the ligand/metal ion mole ratio.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 9 (1980), S. 183-196 
    ISSN: 1572-8927
    Keywords: Macrocyclic complexes ; crown ethers ; lithium ion ; lithium-7 NMR ; complexation constants ; calorimetry ; enthalpy of complexation ; entropy of complexation ; nonaqueous solvents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lithium-7 NMR studies have been carried out on lithium ion complexes with crown ethers 12C4, 15C5, and 18C6 in water and in several nonaqueous solvents. In all cases the exchange between the free and complexed lithium ion was fast on the NMR time scale, and a single, population average, resonance was observed. Both 1:1 and 2:1 (sandwich) complexes were observed between lithium ion and 12C4 in nitromethane solution. The stability of the complexes varied very significantly with the solvent. With the exception of pyridine, the stability varies inversely with the Gutmann donor number of the solvent. In general, the stability order of the complexes was found to be 15C5·Li+〉12C4·Li+〉18C6·Li+. Calorimetric studies on these complexes show that, in most cases, the complexes are both enthalpy and entropy stabilized.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-8927
    Keywords: Crown ethers ; sodium-23 NMR ; cesium-133 NMR ; thallium-205 NMR ; nonaqueous solvents ; enthalpy of complexation ; entropy of complexation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Formation constants for complexes of dibenzo-21-crown-7, dibenzo-24-crown-8 and dibenzo-27-crown-9 with the Na+, Cs+ and Tl+ ions have been determined by multinuclear NMR measurements in several nonaqueous solvents. The measurements of the cesium complexes were carried out at different temperatures and the enthalpy and entropy of complexation were determined from the temperature dependence of the formation constants. The stabilities of these complexes in solvents of low to medium donicity, —nitromethane, acetonitrile, acetone, methanol, and propylene carbonate, vary in the order Tl+〉Cs+〉Na+. Depending on the relative sizes of the cation and of the ligand cavity, either a three-dimensional ‘wrap-around’ complex or a two-dimensional ‘crown complex’ are formed. For the cesium complexes, the values of ΔH c o and ΔS c o are definitely solvent-dependent and in all cases the complexes are enthalpy stabilized but entropy destabilized. A compensating effect is observed in the variation of the enthalpy and entropy of complexation so that the overall influence of the above solvents on the stability of the complexes is rather limited.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-8927
    Keywords: Solvation ; ion pairs ; hexafluorophosphate ion ; fluorine-19 NMR ; sodium-23 NMR ; nonaqueous solvents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Fluorine-19 and sodium-23 NMR measurements were carried out on sodium hexafluorophosphate solutions in a number of solvents. In solvents of medium polarity and donicity (e.g., propylene carbonate, acetone, acetonitrile) the 19 F chemical shift moved upfield with increasing concentration of the salt. This behavior is indicative of anion-cation interactions which may be of long-range type, i.e., formation of solvent-separated ion pairs; the possibility of contact ion pair formation, however, cannot be excluded. In solvents of low polarity and donicity (acetic acid, tetrahydrofuran), the salt is essentially completely associated in the 0.1–1.0M concentration range. On the other hand, in solvating solvents with high dielectric constants, such as dimethyl-formamide, dimethylsulfoxide, and formamide, there is very little ionic association in the same concentration range. The above conclusions are supported by 23 Na chemical shift measurements. Potassium hexafluorophosphate solutions do not show any concentration dependence of the 19 F chemical shifts, while for tetra-n-butylammonium solutions the 19 F resonance moves downfield with increasing concentration of the salt.
    Type of Medium: Electronic Resource
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