Liquids that consist of a mixture of an alcohol and either an amidine or a guanidine have been developed to
switch from a low-polarity form to a high-polarity ionic liquid upon treatment with CO2 at atmospheric pressure.
Treatment with N2 and/or mild heat (50−60 °C) reverses the process. These liquids can be used as switchable
solvents to dissolve and then precipitate a solute or to dissolve reagents for a chemical synthesis and then
precipitate the product.
A five-coordinate chloride ion is believed to template the assembly of a pentadecanuclear lanthanide complex of europium(III). This cluster (see picture) has been prepared by coordination of europium(III) perchlorate with tyrosine at about pH 6. Single crystal X-ray analysis established an unprecedented structure in which 15 constituent europium(III) ions are organized into three parallel pentagonal layers.
We report a comprehensive variable-temperature solid-state 17 O NMR study of three 17 O-labeled crystalline sulfonic acids: 2-aminoethane-1-sulfonic acid (taurine, T), 3-aminopropane-1-sulfonic acid (homotaurine, HT), and 4-aminobutane-1-sulfonic acid (ABSA − groups in these compounds undergo a 3-fold rotational jump mechanism but also extracted the corresponding jump rates (10 2 −10 5 s −1 ) and the associated activation energies (E a ) for this process (E a =4 8± 7, 42 ± 3, and 45 ± 1 kJ mol −1 for T, HT, and ABSA, respectively). This is the first time that SO 3 − rotational dynamics have been directly probed by solid-state 17 O NMR. Using the experimental activation energies for SO 3 − rotation, we were able to evaluate quantitatively the total hydrogen bond energy that each SO 3 − group is involved in within the crystal lattice. The activation energies also correlate with calculated rotational energy barriers. This work provides a clear illustration of the utility of solid-state 17 O NMR in quantifying dynamic processes occurring in organic solids. Similar studies applied to selectively 17 O-labeled biomolecules would appear to be very feasible.
A series of pentadecanuclear lanthanide-hydroxo complexes possessing a common core of the formula [Ln(15)(mu(3)-OH)(20)(mu(5)-X)](24+)(1, Ln = Eu, X = Cl(-); 2, Ln = Nd, X = Cl(-); 3, Ln = Gd, X = Cl(-); 4, Ln = Pr, X = Br(-); 5, Ln = Eu, X = Br(-)) were prepared by L-tyrosine-controlled hydrolysis of corresponding lanthanide perchlorates in the presence of added Cl(-) or Br(-). The cationic cluster core comprises five vertex-sharing cubane-like [Ln(4)(mu(3)-OH)(4)](8+) units centered on the halide template. In the case of templating I(-), dodecanuclear complexes were isolated instead. The core component, [Ln(12)(mu(3)-OH)(16)(I)(2)](18+) (6, Ln = Dy; 7, Ln = Er), consists of four vertex-sharing cubane-like [Ln(4)(mu(3)-OH)(4)](8+) units and exists as a square-shaped cyclic structure with one I(-) located on each side of the square plane. An analogous hydrolytic reaction involving Er(NO(3))(3), L-tyrosine, and NaOH affords the known hexanuclear complex [Er(6)(mu(6)-O)(mu(3)-OH)(8)(NO(3))(6)(H(2)O)(12)](NO(3))(2) whose core component is a face-capped octahedral [Er(6)(mu(6)-O)(mu(3)-OH)(8)](8+) cluster with an interstitial mu(6)-oxo group (Wang, R.; Carducci, M. D.; Zheng, Z. Inorg. Chem. 2000, 39, 1836-1837.). The efficient self-assembly of halide-encapsulating multicubane complexes (1-7) and the inability to produce an analogous nitrate-containing complex demonstrate the superior templating roles played by the halide ion(s). Further credence for the halide template effects was provided by the isolation of the cationic pentadecanuclear complex 3 as the sole product when tyrosine-supported hydrolysis of Gd(NO(3))(3) was carried out in the presence of competitive Cl(-). Magnetic moments of complexes 1-7 measured at room temperature by using Evans' method are in excellent agreement with those calculated by the Van Vleck equation, assuming magnetically noninteractive lanthanide ions.
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