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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 12 (1992), S. 377-387 
    ISSN: 1573-1111
    Keywords: Charles Pedersen ; crown ethers ; phenol-pendant cyclam-zinc(II) complex ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molecular structure of phenol-pendant cyclam-zinc(II) complex,4a, has been determined by X-ray structure analysis. Crystals of4a · ClO4 · CH3OH (C16H27N4OZn · ClO4 · CH3OH) are monoclinic, space groupP21/nn, with four molecules in the unit cell of dimensionsa=31.198(2) Å,b=8.426(1) Å,c=8.214(1) Å, andβ=93.96(1)°. The structure was solved by the heavy atom method and refined anisotropically toR=0.044,R w=0.062 for 1551 independent reflections. The complex assumes a five-coordinate, square pyramidal geometry, where zinc(II) is surrounded by the cyclam moiety in a planar fashion with the pendant phenolate anion occupying an axial position. An extremely short Zn-O(phenolate) bond distance of 1.983(5) Å, in conjunction with the 0.288 Å displacement of Zn(II) above the cyclam N4 plane toward the phenolate, accounts for the extremely low pK a value of 5.8 for the pendant phenol. These facts about4a, in comparison with the previous findings for the Ni(II) (4b) and Cu(II) complexes (4c) with the same ligand, illustrate well the characteristics of zinc(II) ion coordination properties.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 617-623 
    ISSN: 0947-6539
    Keywords: barbiturates ; macrocycles ; molecular recognition ; receptors ; zinc complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new bis-zinc(II) receptor (Zn2L), which has two macrocyclic 12-membered tetraamine (cyclen) ZnII complexes connected through a p-xylene bridge, has been synthesized as a novel host molecule to recognize barbiturates (such as barbital (bar)) in aqueous solution. Each of the zinc(II) ions in the biszinc(II) receptor was originally intended to match the dianionic barbital anion (bar2-) with supplementary hydrogen bonds between the cyclen NH's and the three carbonyl oxygens in complementary positions to yield a 1:1 complex, Zn2L-bar2-. From an aqueous solution of equimolar Zn2L and barbital at pH 8, however, a cyclic 2:2 complex, (Zn2L-bar2-)2, was isolated and characterized by X-ray crystal analysis. The NMR study in 10% (v/v) D2O/H2O has revealed dissociation of (Zn2L-bar2-)2 solely into the original target 1:1 complex Zn2L-bar2- and established the dimerization constant for 2Zn2L-bar2- → (Zn2L-bar2-)2, Kd ( = [(Zn2L-bar2-)2]/[Zn2L-bar2-]2) to be 103.4 M-1. The thermodynamic parameters were evaluated from the NMR measurements at 25, 35, 45, and 55°C: ΔG = -1.9 × 104 J mol-1, ΔH = - 3.3 × 104 J mol-1, ΔS = - 49 J mol-1 K-1 at 25°C. Potentiometric pH titration of Zn2L (1 mM) and barbital (1 mM) disclosed extremely facile deprotonation of the two imido groups of barbital at pH less than 7 to form the dianionic barbital-bound ZnII complexes Zn2L-bar2- and (Zn2L-bar2-)2, where-by the barbital binding affinity for Zn2L was estimated to be Kbar ( = [Zn2L-bar2-]/[uncomplexed Zn2L][uncomplexed barbital]) = 105.8 M-1 at pH 8 and 25°C with I = 0.10 (NaNO3). The significance of the bis-zinc(II) receptor in stabilizing the dianionic barbital is evident by comparison with the interaction of ZnII-cyclen complex (ZnL) with barbital, which yields only a 1:1 monoanionic barbital complex, ZnL-bar- (Kbar = [ZnL-bar-]/[uncomplexed ZnL][uncomplexed barbital] = 104.2M-1 at pH 8 and 25°C with I = 0.10 (NaNO3)).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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