Department of Chemistry, University of Minnesota, 207 Pleasant Street SE, Minneapolis Minnesota 55455, USA.
J Am Chem Soc. 2011 Dec 28;133(51):20869-77. doi: 10.1021/ja207680e. Epub 2011 Dec 2.
Manganese(III) complexes of three fluorophilic salen derivatives were used to prepare ion-selective electrodes (ISEs) with ionophore-doped fluorous sensing membranes. Because of their extremely low polarity and polarizability, fluorous media are not only chemically very inert but also solvate potentially interfering ions poorly, resulting in a much improved discrimination of such ions. Indeed, the new ISEs exhibited selectivities for CO(3)(2-) that exceed those of previously reported ISEs based on nonfluorous membranes by several orders of magnitude. In particular, the interference from chloride and salicylate was reduced by 2 and 6 orders of magnitude, respectively. To achieve this, the selectivities of these ISEs were fine-tuned by addition of noncoordinating hydrophobic ions (i.e., ionic sites) into the sensing membranes. Stability constants of the anion-ionophore complexes were determined from the dependence of the potentiometric selectivities on the charge sign of the ionic sites and the molar ratio of ionic sites and the ionophore. For this purpose, a previously introduced fluorophilic tetraphenylborate and a novel fluorophilic cation with a bis(triphenylphosphoranylidene)ammonium group, (R(f6)(CH(2))(3))(3)PN(+)P(R(f6)(CH(2))(3))(3), were utilized (where R(f6) is C(6)F(13)). The optimum CO(3)(2-) selectivities were found for sensing membranes composed of anionic sites and ionophore in a 1:4 molar ratio, which results in the formation of 2:1 complexes with CO(3)(2-) with stability constants up to 4.1 × 10(15). As predicted by established theory, the site-to-ionophore ratios that provide optimum potentiometric selectivity depend on the stoichiometries of the complexes of both the primary and the interfering ions. However, the ionophores used in this study give examples of charges and stoichiometries previously neither explicitly predicted by theory nor shown by experiment. The exceptional selectivity of fluorous membranes doped with these carbonate ionophores suggests their use not only for potentiometric sensing but also for other types of sensors, such as the selective separation of carbonate from other anions and the sequestration of carbon dioxide.
使用三种亲氟沙仑衍生物的三价锰配合物,制备了具有离子载体掺杂氟感测膜的离子选择性电极 (ISE)。由于其极低的极性和极化率,氟碳介质不仅在化学上非常惰性,而且对潜在干扰离子的溶剂化作用也很差,从而大大提高了对这些离子的选择性。实际上,新型 ISE 对 CO(3)(2-)的选择性超过了先前报道的基于非氟膜的 ISE 几个数量级。特别是,氯离子和水杨酸盐的干扰分别降低了 2 和 6 个数量级。为了实现这一目标,通过向传感膜中添加非配位疏水离子(即离子位)来微调这些 ISE 的选择性。通过依赖于离子位的电荷符号和离子位与离子载体的摩尔比来确定阴离子-离子载体配合物的稳定常数。为此,利用了先前引入的亲氟四苯硼酸盐和一种新型具有双(三苯基膦亚基)铵基团的亲氟阳离子,(R(f6)(CH(2))(3))(3)PN(+)P(R(f6)(CH(2))(3))(3)(其中 R(f6) 是 C(6)F(13))。在阴离子位和离子载体摩尔比为 1:4 的传感膜中发现了最佳的 CO(3)(2-)选择性,这导致与 CO(3)(2-)形成 2:1 配合物,稳定常数高达 4.1×10(15)。正如既定理论所预测的,提供最佳电位选择性的位-载体比取决于主离子和干扰离子的配合物的化学计量。然而,本研究中使用的离子载体提供了电荷和化学计量的例子,这些例子以前既没有被理论明确预测,也没有被实验证明。用这些碳酸根离子载体掺杂的氟碳膜具有出色的选择性,这表明它们不仅可用于电位传感,还可用于其他类型的传感器,例如从其他阴离子中选择性分离碳酸根和二氧化碳的螯合。