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SALICYLATE SELECTIVE ELECTRODE BASED ON A BIOMIMETIC GUANIDINIUM IONOPHORE

机译:基于仿生胍离子的水杨酸选择性电极

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A biomimetic strategy was employed in the development of oxoanion-selective ionophores containing the guanidinium functional group. These ionophores mimic the selective interaction observed between arginine residues of proteins and oxoanions. In previous work, it was demonstrated that a structurally rigid guanidinium ionophore exhibited excellent hydrogen sulfite selectivity (Anal, Chem. 1994, 66, 3188-3192). Herein, we describe guanidinium-containing ionophores that are selective for the oxoanion salicylate. The ability to rationally design anion-selective electrodes through this biomimetic strategy, and to both alter selectivity and improve response characteristics through structural changes to the ionophore, has been demonstrated. H-1-NMR complexation and modeling studies were used to examine and correlate the selectivity observed with the structure of the guanidinium compounds.
机译:仿生策略被用于开发含有胍基官能团的氧代阴离子选择性离子载体。这些离子载体模拟在蛋白质的精氨酸残基和氧阴离子之间观察到的选择性相互作用。在先前的工作中,已经证明结构上刚性的胍盐离子载体表现出优异的亚硫酸氢选择性(Anal,Chem.1994,66,3188-3192)。在本文中,我们描述了对水杨酸阴离子有选择性的含胍盐的离子载体。通过这种仿生策略合理设计阴离子选择电极,并通过改变对离子载体的结构来改变选择性和改善响应特性的能力已得到证明。使用H-1-NMR络合和模型研究来检查观察到的选择性并将其与胍化合物的结构相关联。

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