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亲脂性镧系三(β-二酮)配合物作为用于氯离子选择性电极的离子载体。

Lipophilic lanthanide tris(beta-diketonate) complexes as an ionophore for Cl- anion-selective electrodes.

作者信息

Mahajan Rakesh Kumar, Kaur Inderpreet, Kaur Ravneet, Onimaru Aki, Shinoda Satoshi, Tsukube Hiroshi

机构信息

Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, India.

出版信息

Anal Chem. 2004 Dec 15;76(24):7354-9. doi: 10.1021/ac0497858.

Abstract

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.

摘要

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。

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