Mahajan Rakesh Kumar, Kaur Inderpreet, Kaur Ravneet, Onimaru Aki, Shinoda Satoshi, Tsukube Hiroshi
Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, India.
Anal Chem. 2004 Dec 15;76(24):7354-9. doi: 10.1021/ac0497858.
A series of novel anion-selective electrodes were developed by incorporating lipophilic lanthanide tris(beta-diketonates) into plasticized poly(vinyl chloride) membranes. The new electrodes exhibited high selectivity toward Cl(-) anion in the concentration range of Cl(-) anion between 1.0 x 10(-5) and 1.0 x 10(-1) mol/L with near-Nernstian slopes and practically low detection limits. They offered non-Hofmeister anion selectivity, and interestingly discriminated Cl(-) anion from NO(3)(-), ClO(4)(-), and other anions. Since the employed lanthanide tris(beta-diketonates) were confirmed to form 1:1 highly coordinated complexes with Cl(-) anion, the observed high selectivity for Cl(-) anion was attributed to the characteristics of lanthanide coordination chemistry. All the prepared sensors worked well at neutral pH with quite short response time, <30 s, and could be used for longer than four months without any significant divergence in performance.
通过将亲脂性镧系三(β-二酮)掺入增塑聚氯乙烯膜中,开发了一系列新型阴离子选择性电极。新电极在1.0×10⁻⁵至1.0×10⁻¹mol/L的Cl⁻阴离子浓度范围内对Cl⁻阴离子表现出高选择性,具有近能斯特斜率和实际较低的检测限。它们具有非霍夫迈斯特阴离子选择性,有趣的是能将Cl⁻阴离子与NO₃⁻、ClO₄⁻和其他阴离子区分开来。由于所使用的镧系三(β-二酮)被证实与Cl⁻阴离子形成1:1的高配位络合物,因此观察到的对Cl⁻阴离子的高选择性归因于镧系配位化学的特性。所有制备的传感器在中性pH下工作良好,响应时间非常短,<30秒,并且可以使用四个多月而性能没有任何明显差异。