Quantitative evaluation of the ion-binding characteristics of poly(4′-vinylbenzo-18-crown-6)

Cindy C. Chen, Thomas W. Smith
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引用次数: 1

Abstract

We have carried out an in-depth study of the alkali metal ion binding characteristics of a model ionophoric macromolecule, poly(4′-vinylbenzo 18-crown-6), P18C6. Ion selective electrode potentiometry has been utilized to determine stability constants for complexstion of K+, Na+, and Cs+ to P18C6 in methanol/water (80/20)w. Our results show that (he intrinsic binding constants, Kn, of P18C6 towards K+C1 and Na+Cl are identical to that of the monomeric analog, benzo-18-crown-6.

In the absence of supporting electrolyte, the apparent binding constant of benzo-18-crown-6 is greater than (hat of P18C6. At low tonic strength the binding of K+ to P18C6 depends strongly on the fraction of crown moieties bound. P18C6 binds K+C1 and Na+Cl with a stoichiometry of 2 mol of crown per mole of M+ . This binding, however, is not sandwich mode. The binding of K+Cl, K+NO3 and K+ClO4 to P18C6 in methanol/water differs significantly, with KN(K+ClO41 being nearly an order of magnitude greater than KN(K+Cl). Cs+ is bound to P1SC6 with a stoichiometry of ∼3 mol of crown per mole of Cs+, and the ion is bound cooperatively in a sandwich geometry.

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聚(4’-乙烯基苯并-18-冠-6)离子结合特性的定量评价
我们深入研究了一种模型电离电大分子聚(4′-乙烯基苯并18-冠-6)P18C6的碱金属离子结合特性。离子选择电极电位法测定了K+、Na+和Cs+在甲醇/水(80/20)w中与P18C6络合的稳定性常数。结果表明,P18C6对K+C1−和Na+Cl−的本征结合常数Kn与单体类似物苯并-18-冠-6相同。在无支撑电解质的情况下,苯并-18-冠-6的表观结合常数大于P18C6。在低强压强度下,K+与P18C6的结合很大程度上取决于结合的树冠部分的比例。P18C6结合K+C1−和Na+Cl−的化学计量量为每摩尔M+ 2mol树冠。然而,这种绑定不是三明治模式。在甲醇/水中,K+Cl−、K+NO3和K+ClO4−与P18C6的结合有显著差异,其中KN(K+ClO4−1)几乎大于KN(K+Cl−)一个数量级。Cs+与P1SC6结合,每摩尔Cs+的化学计量量为~ 3mol王冠,并且离子以三明治几何形式合作结合。
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