Bakker E, Malinowska E, Schiller R D, Meyerhoff M E
Department of Chemistry, The University of Michigan, Ann Arbor, MI 48109, U.S.A.
Talanta. 1994 Jun;41(6):881-90. doi: 10.1016/0039-9140(94)e0041-o.
The role of lipophilic anionic and cationic additives on the potentiometric anion selectivities of polymer membrane electrodes prepared with various metalloporphyrins as anion selective ionophores is examined. The presence of lipophilic anionic sites (e.g. tetraphenylborate derivatives) is shown to enhance the non-Hofmeister anion selectivities of membranes doped with In(III) and Sn(IV) porphyrins. In contrast, membranes containing Co(III) porphyrins require the addition of lipophilic cationic sites (e.g. tridodecylmethylammonium ions) in order to achieve optimal anion selectivity (for nitrite and thiocyanate) as well as rapid and reversible Nernstian response toward these anionic species. These experimental results coupled with appropriate theoretical models that predict the effect of lipophilic anion and cation sites on the selectivities of membranes doped with either neutral or charged carrier type ionophores may be used to determine the operative ionophore mechanism of each metalloporphyrin complex within the organic membrane phase.
研究了亲脂性阴离子和阳离子添加剂对以各种金属卟啉作为阴离子选择性离子载体制备的聚合物膜电极的电位阴离子选择性的影响。结果表明,亲脂性阴离子位点(如四苯基硼酸盐衍生物)的存在可增强掺杂铟(III)和锡(IV)卟啉的膜的非霍夫迈斯特阴离子选择性。相比之下,含有钴(III)卟啉的膜需要添加亲脂性阳离子位点(如三(十二烷基)甲基铵离子),以实现最佳的阴离子选择性(针对亚硝酸盐和硫氰酸盐)以及对这些阴离子物种快速且可逆的能斯特响应。这些实验结果与适当的理论模型相结合,该模型预测了亲脂性阴离子和阳离子位点对掺杂中性或带电载体型离子载体的膜选择性的影响,可用于确定有机膜相中每种金属卟啉配合物的作用离子载体机制。